S. Terashima

发表

A linear space representation of language probability through SVD of N‐gram matrix

F. Itakura, K. Takeda, S. Terashima, 2003 .

Synthesis and matrix metalloproteinase-12 inhibitory activity of ageladine A analogs.

S. Terashima, N. Ando, 2011, Chemical & pharmaceutical bulletin.

1,4-Addition of the methylenecarbonyl unit (-CH2CO-) to dienes

E. Corey, S. Terashima, T. Ravindranathan, 1971 .

An efficient synthesis of optically pure anthracyclinone intermediates by the novel use of microbial reduction

S. Terashima, K. Tamoto, 1983 .

Synthetic studies on the compounds related to neocarzinostatin chromophore. 3. Novel synthesis of a chiral cyclic dienediyne system

K. Nakatani, S. Terashima, K. Arai, 1993 .

Synthetic studies on the compounds related to neocarzinostatin chromophore. 2. Synthesis of the open-chain (E)- and (Z)-dienediyne systems and its application to the synthesis of a strain-released cyclic analogue

K. Nakatani, S. Terashima, Kaoru Yamada, 1992 .

Synthetic studies on the compounds related to neocarzinostatin chromophore. 1. Synthesis of the acyclic (E)- and (Z)-dienediyne systems

K. Nakatani, F. Matsuda, S. Terashima, 1992 .

Stereochemical studies. XLVII. Asymmetric reduction of 2-alkyl-1,3,4-cyclopentanetriones with lithium aluminum hydride decomposed by optically active .BETA.-aminoalcohols. Syntheses of optically active allethrolone and prostaglandin E1.

S. Terashima, K. Kameo, M. Kitamoto, 1977 .

Total synthesis of an enantiomeric pair of FR900482. 2. Syntheses of the aromatic and the optically active aliphatic segments

T. Katoh, S. Terashima, M. Hashimoto, 1997 .

A novel biogenetic type synthesis of (+)-hydantocidin

T. Katoh, S. Terashima, T. Yoshino, 1993 .

Ketene Recognizes 1,3-Dienes in Their s-Cis Forms through [4 + 2] (Diels−Alder) and [2 + 2] (Staudinger) Reactions. An Innovation of Ketene Chemistry

S. Terashima, S. Yamabe, T. Minato, 1999 .

Synthesis of Optically Active and Biologically Active Compounds

S. Terashima, 1993 .

A stereoselective synthesis of the (2R, 3S)- and (2S, 3R)-3-amino-2-hydroxybutyric acid derivatives, the key components of a renin inhibitor and bestatin.

Yuko Kobayashi, S. Terashima, Y. Takemoto, 1992 .

A novel synthesis of the (2R,3S)- and (2S3R)-3-amino-2-hydroxycarboxylic acid derivatives, the key components of a renin inhibitor and bestatin, from methyl (R)- and (S-mandelate

Yuko Kobayashi, S. Terashima, Y. Takemoto, 1990 .

STEREOCHEMICAL STUDIES. XL. A BIOMIMETIC CONVERSION OF L-LYSINE INTO OPTICALLY ACTIVE 2-SUBSTITUTED PIPERIDINES. SYNTHESIS OF D- AND L-PIPECOLIC ACID, AND (S)-(+)-CONIINE FROM L-LYSINE

S. Terashima, S. Yamada, K. Aketa, 1976 .

Stereochemical studies. XL. A biomimetic conversion of L-lysine into optically active 2-substituted piperidines. Syntheses of D- and L-pipecolic acid, and (S) (+)-coniine from L-lysine.

S. Terashima, S. Yamada, K. Aketa, 1976 .

Novel synthesis and antitumor activity of 14,14-difluoro-4-demethoxydaunorubicin

F. Matsuda, S. Terashima, M. Ohsaki, 1989 .

Studies toward the total synthesis of popolohuanone E: enantioselective synthesis of 8-O-methylpopolohuanone E.

O. Ohmori, T. Katoh, S. Terashima, 2001, Organic letters.

Studies toward the Total Synthesis of Popolohuanone E: Enantioselective Synthesis of 8-O-MethylpopolohuanoneE

O. Ohmori, T. Katoh, S. Terashima, 2001 .

Studies toward the synthesis of popolohuanone E: Synthesis of natural (+)-arenarol related to the proposed biogenetic precursor of popolohuanone E

T. Katoh, S. Terashima, M. Itoh, 1997 .

Stereochemical Studies. XXIII. Stereochemistry of the Thermal Isocyanide-Cyanide Rearrangement

N. Ohashi, M. Shibasaki, S. Terashima, 1973 .

Novel syntheses of the carbapenem key intermediates, (3R,4R)-4-acetoxy-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone and (3S,4R)-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-4-carboxymethyl-2-azetidinone, from (S)-ethyl lactate

T. Kawabata, S. Terashima, Yoshio N Ito, 1989 .

A highly stereoselective synthesis of (3S,4S)-statine and (3S,4S)-cyclohexylstatine

S. Terashima, Y. Takemoto, Yoshio N Ito, 1991 .

Synthesis of the 1β-Methylcarbapenem Key Intermediates

S. Terashima, Yoshio N Ito, 1993 .

Synthesis of the 1/β-Methylcarbapenem Key Intermediates

S. Terashima, Yoshio N Ito, 1989 .

A highly stereoselective synthesis of the 1β-methylcarbapenem key intermediate from (R)-3-hydroxybutyric acid☆

Yuko Kobayashi, S. Terashima, Yoshio N Ito, 1992 .

Highly stereocontrolled synthesis of the 1β-methylcarbapenem key intermediate by the reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives with a 4-acetoxy-2-azetidinone

S. Terashima, Yoshio N Ito, A. Sasaki, 1991 .

A novel synthesis of the 1β-methylcarbapenem key intermediate employing the [2+2]-cycloaddition reaction of chlorosulfonyl isocyanate with a 4H-1,3-dioxin derivative

Yuko Kobayashi, S. Terashima, Yoshio N Ito, 1989 .

A novel and efficient synthesis of the key intermediate of 1β-methylcarbapenem antibiotics employing [ 2+2 ]-cycloaddition reaction of diketene with a chiral imine

T. Kawabata, Y. Kimura, S. Terashima, 1988 .

A highly stereoselective synthesis of a key intermediate of 1β-methylcarbapenems employing the reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives

S. Terashima, Yoshio N Ito, 1987 .

A novel and efficient synthesis of the key intermediate of 1β-methylcarbapenem antibiotics from (s)-methyl 3-hydroxy-2-methylpropionate

T. Kawabata, Y. Kimura, S. Terashima, 1986 .

Synthetic studies on duocarmycin. 2. Synthesis and cytotoxicity of natural (+)-duocarmycin A and its three possible stereoisomers.

K. Nakatani, S. Terashima, Y. Fukuda, 1994 .

Synthesis and cytotoxicity of enantiomeric pairs of duocarmycin a and its 2-epimer

K. Nakatani, S. Terashima, Y. Fukuda, 1992 .

DNA alkylation properties of the duocarmycins: (+)-duocarmycin A, epi-(+)-duocarmycin A, ent-(−)-duocarmycin A and epi,ent-(−)-duocarmycin A

D. Boger, K. Nakatani, S. Terashima, 1992 .

First total synthesis of dl-duocarmycin A

K. Nakatani, S. Terashima, Yoshio N Ito, 1990 .

Total Synthesis of Nogalamycin Congeners and their Related Compounds1

F. Matsuda, S. Terashima, 1994 .

A novel synthesis of the 2-amino-1H-imidazol-4-carbaldehyde derivatives and its application to the efficient synthesis of 2-aminoimidazole alkaloids, oroidin, hymenidin, dispacamide, monobromodispacamide, and ageladine A

S. Terashima, N. Ando, 2010 .

Synthesis of novel ageladine A analogs showing more potent matrix metalloproteinase (MMP)-12 inhibitory activity than the natural product.

Naoki Ando, Shiro Terashima, S. Terashima, 2009, Bioorganic & medicinal chemistry letters.

Synthesis and matrix metalloproteinase (MMP)-12 inhibitory activity of ageladine A and its analogs.

Naoki Ando, Shiro Terashima, S. Terashima, 2007, Bioorganic & medicinal chemistry letters.

Highly stereoselective reformatsky reactions of 3-(2-Bromopropionyl)-2-oxazolidone derivatives with various aldehydes

S. Terashima, Yoshio N Ito, 1991 .

Stereospecific total synthesis of prostaglandins E3 and F3 alpha.

E. Corey, S. Terashima, H. Shirahama, 1971, Journal of the American Chemical Society.

Synthesis and Cytotoxicity of Various Structural Types of Novel Cyclopropapyrroloindole(CPI) Derivatives

H. Furuta, S. Terashima, Y. Oomori, 1998 .

Total Synthesis of Quinocarcin and Its Related Compounds

T. Katoh, S. Terashima, 1998 .

Synthetic studies on quinocarcin and its related compounds. 2.

Katsunori Tanaka, K. Nakatani, F. Matsuda, 1994 .

Synthetic studies on quinocarcin and its related compounds. 1. Synthesis of enantiomeric pairs of the ABE ring systems of quinocarcin

F. Matsuda, Yuko Kobayashi, T. Katoh, 1994 .

A novel synthesis of (+)-duocarmycin SA

S. Terashima, Y. Fukuda, 1997 .

Asymmetric synthesis of (1R,2S)-2-fluorocyclopropylamine, the key intermediate of the new generation of quinolonecarboxylic acid, DU-6859

K. Nakatani, Yuko Kobayashi, T. Katoh, 1992 .

Chiral synthesis of the def-ring system of nogalamycin

F. Matsuda, S. Terashima, M. Kawasaki, 1985 .

A novel synthesis of the α-hydroxyketone moiety of anthracyclinones by the use of 2-trimethylsilylethynylcerium(III) reagents

Y. Kimura, S. Terashima, Michiyo Suzuki, 1984 .

An Improved Synthesis of N-Trifluoroacetyl-L-daunosamine

Y. Kimura, S. Terashima, Teruyo Matsumoto, 1986 .

Synthetic studies on the key component of the new generation of quinolonecarboxylic acid, DU-6859. 2.

K. Nakatani, Yuko Kobayashi, T. Katoh, 1994 .

A novel and highly efficient asymmetric synthesis of optically active anthracyclinones

Y. Kimura, S. Terashima, Michiyo Suzuki, 1986 .

AN IMPROVED ASYMMETRIC SYNTHESIS OF (R)-(−)-2-ACETYL-5,8-DIMETHOXY-1,2,3,4-TETRAHYDRO-2-NAPHTHOL. A VERSATILE KEY SYNTHETIC INTERMEDIATE OF OPTICALLY ACTIVE ANTHRACYCLINONES

Y. Kimura, S. Terashima, Michiyo Suzuki, 1985 .

A general and highly efficient asymmetric synthesis of optically active anthracyclinones

Y. Kimura, S. Terashima, Michiyo Suzuki, 1985 .

A novel enantioselective synthesis of the key intermediate of (−)-huperzine a employing asymmetric palladium-catalyzed bicycloannulation

T. Katoh, S. Terashima, T. Yoshino, 1997 .

Synthetic studies on the key component of the new generation of quinolonecarboxylic acid, DU-6859. 1. Synthesis of (1R,2S)-2-fluorocyclopropylamine by the use of optical resolution

K. Nakatani, Yuko Kobayashi, T. Katoh, 1994 .

Amino acids and peptides—V

S. Terashima, M. Wagatsuma, S. Yamada, 1973 .

(Acetylacetonato)[(-)-N-alkylephedrinato]dioxomolybdenum, a new class of chiral chelate complexes which catalyze asymmetric epoxidation of allylic alcohol

S. Terashima, T. Mashiko, S. Yamada, 1977 .

A stereoselective synthesis of cyclohexylnorstatine, the key component of a renin inhibitor

Yuko Kobayashi, S. Terashima, Y. Takemoto, 1990 .

A novel synthesis of cyclohexylnorstatine isopropyl ester, the C-terminal component of a renin inhibitor

S. Terashima, Yoshio N Ito, H. Harada, 1990 .

An expeditious synthesis of (3S,4S)-statine and (3S,4S)cyclohexylstatine

S. Terashima, Y. Takemoto, Yoshio N Ito, 1990 .

Asymmetric halolactonisation reaction—4

K. Koga, S. Terashima, M. Hayashi, 1981 .

A highly efficient asymmetric synthesis of optically active α,β-epoxyaldehydes from α,β-unsaturated acids

K. Koga, S. Terashima, M. Hayashi, 1980 .

Asymmetric reduction of αβ-unsaturated ketones with lithium aluminium hydride partially decomposed by (–)-N-methylephedrine and N-ethylaniline

K. Koga, S. Terashima, N. Tanno, 1980 .

Synthesis of the 1β‐Methylcarbapenem Key Intermediates

S. Terashima, Yoshio N Ito, 2010 .

A novel synthesis of (3R,4R)-4-acetoxy-3-[(R)-1-(t-butyldimethylsilyloxy)ethyl]-2-azetidinone, the versatile key intermediate of carbapenem synthesis, from (S)-ethyl lactate

T. Kawabata, S. Terashima, Yoshio N Ito, 1986 .

Synthetic studies of huperzine A and its fluorinated analogues. 2. Synthesis and acetylcholinesterase inhibitory activity of novel fluorinated huperzine A analogues

N. Nakajima, T. Katoh, S. Terashima, 1998 .

Synthetic studies of huperzine A and its fluorinated analogues. 1. Novel asymmetric syntheses of an enantiomeric pair of huperzine A

T. Katoh, S. Terashima, T. Yoshino, 1998 .

Practical synthesis of (2s,3s)-3-amino-2-hydroxy-4-phenylbutyric acid, a key component of HIV protease inhibitors.

S. Terashima, N. Shibata, E. Itoh, 1998, Chemical & pharmaceutical bulletin.

A Novel and Efficient Synthesis of the Key Intermediate of 1β-Methylcarbapenem Antibiotics Employing (2 + 2) Cycloaddition Reaction of Diketene with a Chiral Imine.

T. Kawabata, Y. Kimura, S. Terashima, 1988 .

A Novel Synthesis of the 1β-Methylcarbapenem Key Intermediate Employing the (2 + 2)Cycloaddition Reaction of Chlorosulfonyl Isocyanate with a 4H-1,3-Dioxin Derivative.

Yuko Kobayashi, S. Terashima, Yoshio N Ito, 1990 .

A Highly Stereoselective Synthesis of the 1β‐Methylcarbapenem Key Intermediate from (R)‐3‐Hydroxybutyric Acid.

Yuko Kobayashi, S. Terashima, Yoshio N Ito, 1992 .

An Improved Synthetic Method of (S)-2-Alkoxypropanals from Ethyl (S)-Lactate

Yuko Kobayashi, S. Terashima, Yoshio N Ito, 1989 .

A Novel and Efficient Synthesis of the Key Intermediate of 1β-Methylcarbapenem Antibiotics from (S)-Methyl 3-Hydroxy-2-methylpropionate.

T. Kawabata, Y. Kimura, S. Terashima, 1987 .

Synthetic studies on quinocarcin and its related compounds. 3.

Yuko Kobayashi, T. Katoh, S. Terashima, 1994 .

(4R,5S)‐4,5‐Diphenyl‐3‐Vinyl‐2‐Oxazolidinone

S. Terashima, O. Tamura, T. Akiba, 2003 .

Synthetic studies on nogalamycin congeners [2]1,2 chiral synthesis of the cdef-ring system of nogalamycin

F. Matsuda, S. Terashima, M. Kawasaki, 1988 .

Novel Ethynylcerium(III) Reagents as Efficient Tools for Constructing the α-Hydroxy Methyl Ketone Moiety of Anthracyclinones

Y. Kimura, S. Terashima, Michiyo Suzuki, 1986 .

Asymmetric halolactonisation reaction—1

K. Koga, S. Terashima, S. Jew, 1979 .

Synthetic studies of himbacine, a potent antagonist of the muscarinic M2 subtype receptor 1. Stereoselective total synthesis and antagonistic activity of enantiomeric pairs of himbacine and (2′S,6′R)-diepihimbacine, 4-epihimbacine, and novel himbacine congeners

T. Katoh, S. Terashima, A. Ishiwata, 2002 .

Total synthesis of natural (+)-FR900482. 2. Efficient syntheses of the aromatic and the optically active aliphatic fragments

T. Katoh, S. Terashima, M. Hashimoto, 1996 .

Asymmetric reduction of prochiral cyclic ketones with lithium aluminum hydride partially decomposed by (1R, 2S)-(−)-N-methylephedrine and 2-alkylaminopyridine

S. Terashima, M. Kawasaki, Yasutaka Suzuki, 1984 .

Asymmetric halolactonization reaction: a highly efficient synthesis of optically active α-hydroxy acids from α,β-unsaturated acids

S. Terashima, S. Jew, 1977 .

Stereochemical Studies. XXIX. Asymmetric Synthesis of 2-Alkylcyclohexanones via optically Active Lithioenamines

S. Terashima, K. Hiroi, M. Kitamoto, 1974 .

Stereochemical Studies. I. Elucidation of the Reaction Mechanism of the Base-induced Rearrangement of Ketone Trimethylhydrazonium Iodide using optically Active Compounds

S. Terashima, S. Yamada, 1968 .

Enantioselective synthesis of 5-substituted- and 3,5-disubstituted-2-formylpyrrolidine derivatives, the key D-ring fragments of (−)-quinocarcin and (−)-10-decarboxyquinocarcin

T. Katoh, S. Terashima, Y. Nagata, 1993 .

Chiral synthesis of the ABC-ring system of quinocarcin

Katsunori Tanaka, K. Nakatani, F. Matsuda, 1989 .

Stereochemical studies—LVII: Synthesis of optically active compounds by the novel use of meso-compounds—1. Efficient synthesis of two structural types of optically pure prostaglandin intermediates

S. Terashima, S. Yamada, M. Nara, 1980 .

Stereochemical Studies. XLI. Asymmetric Synthesis of optically Active 4a-Methyl-4, 4a, 9, 10-tetrahydro-2 (3H)-phenanthrone Derivatives, Key Intermediates for Total Syntheses of optically Active Diterpenes and Steroids

S. Terashima, T. Sone, S. Yamada, 1976 .

Total synthesis of natural (+)-FR900482. 1. Synthetic and end-game strategies

T. Katoh, S. Terashima, T. Yoshino, 1996 .

Stereochemical Studies. XLIV. Exploitation of the New Synthetic Scheme for Chiral Additives Usable in Asymmetric Syntheses. Novel Syntheses of optically Active γ-Amino Acids and Pyrrolidines from L-α-Amino Acids

S. Terashima, C. Tseng, S. Yamada, 1977 .

Novel cyclopropapyrroloindole derivative (AT-3510) bearing methoxycarbonyl and trifluoromethyl groups.

H. Furuta, S. Terashima, Y. Oomori, 1999, Journal of medicinal chemistry.

Studies on Optically Active Amino Acids. XIV. Studies on α-Alkyl-α-amino acids. VII. Determination of Absolute Configuration of Optically Active α-Methylphenylglycine Configuration of Optically Active α-Methylphenylglycine and 1-Methyl-1-phenylpropylamine.

K. Achiwa, S. Terashima, S. Yamada, 1967 .

Determination of the absolute configuration of alpha-methylphenylglycine by the thermal decomposition of the azidoformate.

K. Achiwa, S. Terashima, S. Yamada, 1966, Chemical & pharmaceutical bulletin.

Synthesis and antitumor activity of novel cyclopropapyrroloindole (CPI) derivatives bearing bis(methoxycarbonyl) groups

S. Terashima, Y. Oomori, Y. Fukuda, 1997 .

Synthetic Studies on Duocarmycin. Part 2. Synthesis and Cytotoxicity of Natural (+)-Duocarmycin A and Its Three Possible Stereoisomers.

K. Nakatani, S. Terashima, Y. Fukuda, 1994 .

The novel cyclopropapyrroloindole(CPI) bisalkylators bearing methoxycarbonyl and trifluoromethyl groups.

H. Furuta, S. Terashima, Y. Oomori, 1998, Bioorganic & medicinal chemistry letters.

Synthesis and antitumor activity of novel cyclopropapyrroloindole(CPI) derivatives bearing methoxycarbonyl and trifluoromethyl groups

H. Furuta, S. Terashima, F. Shiga, 1997 .

First Total Synthesis of dl‐Duocarmycin A (I).

K. Nakatani, S. Terashima, Yoshio N Ito, 1992 .

Synthetic Studies on Duocarmycin. Part 1. Total Synthesis of dl‐ Duocarmycin A and Its 2‐Epimer.

K. Nakatani, S. Terashima, Y. Fukuda, 1994 .

Synthesis of optically Active α-Alkyl or α-Aryl Acids from L-α-Amino Acids by the Use of Organocopper Reagents

K. Koga, S. Terashima, C. Tseng, 1979 .

Synthesis, chemical property, and cytotoxicity of the carzinophilin congeners carrying a 2-(1-acylamino-1-alkoxycarbonyl)methylidene-1-azabicyclo[3.1.0]hexane system

S. Terashima, M. Hashimoto, Kaoru Yamada, 1994 .

A Stereoselective Synthesis of a Novel Model Compound of Carzinophilin Carrying the C6-C13 Unit with Correct Stereochemistry.

S. Terashima, M. Hashimoto, 1994 .

Synthetic studies of carzinophilin. Part 2: Synthesis of 3,4-dibenzyloxy-2-methylidene-1-azabicyclo[3.1.0]hexane systems corresponding to the C1–C17 fragment of carzinophilin

S. Terashima, M. Hashimoto, M. Matsumoto, 2003 .

A Stereoselective Synthesis of a Novel Model Compound of Carzinophilin Carrying the C6-C13 Unit with Correct Stereochemistry

S. Terashima, M. Hashimoto, 1994 .

11,15-Epiprostaglandin E 2 and its enantiomer. Biological activity and synthesis.

E. Corey, D. Floyd, S. Terashima, 1972, The Journal of organic chemistry.

A dramatic change in the balance between SN2 and E2 pathways with formate and oxalate as nucleophile

E. Corey, S. Terashima, 1972 .

A highly stereoselective synthesis of aldols employing the Reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives with various aldehydes

S. Terashima, Yoshio N Ito, 1987 .

Amino acids and peptides—IV

S. Terashima, M. Wagatsuma, S. Yamada, 1973 .

A Synthesis of (3S,4R)-3-[(R)-1-(t-Butyldimethylsilyloxy)ethyl]-4-carboxymethyl-2-azetidinone, the Thienamycin Intermediate, from (S)-Ethyl Lactate

S. Terashima, Yoshio N Ito, 1987 .

Asymmetric Synthesis of optically Active Anthracyclinone Intermediate and 4-Demethoxyanthracyclinones by the Use of a Novel Chiral Reducing Agent

S. Terashima, N. Tanno, 1983 .

Synthesis of Anthracycline Antibiotics.

S. Terashima, 1982 .

Efficient synthesis and antitumor activity of an enantiomeric pair of the sesbanimide AB-ring systems

F. Matsuda, S. Terashima, M. Kawasaki, 1985 .

Asymmetric halolactonisation reaction-2

K. Koga, S. Terashima, S. Jew, 1979 .

Synthetic studies of carzinophilin. Part 3: Synthetic approach toward carzinophilin and successful synthesis of 13-O-desacetyl-12,13-di-O-benzyl-4-O-methylcarzinophilin

S. Terashima, M. Sugiura, M. Hashimoto, 2003 .

Novel synthesis of a chiral cyclic dienediyne system related to the neocarzinostatin chromophore

K. Nakatani, S. Terashima, K. Arai, 1992 .

A simple and efficient synthesis of optically active (+)-4-demethoxydaunomycinone.

Y. Kimura, S. Terashima, Teruyo Matsumoto, 1986 .

2-Chloro-1,3-butadiene as an efficient enophile in the Diels-Alder reaction with anthracene-1,4,9,10-tetraone. A simple synthesis of the 4-demethoxyanthracyclinone intermediate

Y. Kimura, S. Terashima, R. Abe, 1984 .

Synthesis of 14,14-difluoro-4-demethoxydaunorubicin

F. Matsuda, S. Terashima, M. Ohsaki, 1991 .

Novel resolution of the anthracyclinone intermediate by the use of (2r, 3r)-(+)- and (2s, 3s)-(-).1,4-bis(4-chlorobenzyloxy)butane-2,3-diol: a simple and efficient synthesis of optically pure 4-demethoxydaunomycinone and 4-demethoxyadriamycinone☆

S. Terashima, M. Sugimori, K. Tamoto, 1984 .

Asymmetric synthesis of optically active anthracyclinones

K. Koga, S. Terashima, S. Jew, 1979 .

Asymmetric synthesis of (R)-(−)−2-acetyl-1,2,3,4-tetrahydro-2-naphthol: a model study for the synthesis of optically active anthracyclinones

K. Koga, S. Terashima, S. Jew, 1977 .

(+)- and (-)-1-0, 4-0-bis(p-chlorobenzyl)threitol as novel resolving agents for optically active anthracyclinone synthesis: an efficient synthesis of optically pure 4-demethoxydaunomycinone

S. Terashima, M. Sugimori, K. Tamoto, 1982 .

Synthesis of various model compounds for the central tricyclic ring system of popolophuanone E

T. Katoh, S. Terashima, Y. Ueki, 1996 .

TOTAL SYNTHESIS OF AN ENANTIOMERIC PAIR OF FR900482. 1. SYNTHETIC AND END-GAME STRATEGIES

T. Katoh, S. Terashima, T. Yoshino, 1997 .

Total Synthesis of Nogalamycin Congeners and Their Related Compounds

F. Matsuda, S. Terashima, 1994 .

Synthetic studies on nogalamycin congeners. Total syntheses of (+)-nogarene, (+)-7-con-O-methylnogarol, and their related compounds

F. Matsuda, S. Terashima, M. Kawasaki, 1989 .

Syntheses and cytotoxicity of various 7-methoxynogarene derivatives.

F. Matsuda, S. Terashima, M. Kawasaki, 1988 .

Synthetic studies on nogalamycin congeners [3]1,2 total syntheses of (+)-nogarene, (+)-7-deoxynogarol, and (+)-7-con-o-methylnogarol

F. Matsuda, S. Terashima, M. Kawasaki, 1988 .

Synthetic studies on nogalamycin congeners [4]1,2 syntheses amd antitumor activity of various nogalamycin congeners

F. Matsuda, S. Terashima, M. Kawasaki, 1988 .

First total syntheses of (+)-7-deoxynogarol and (+)-7-con-o-methylnogarol

F. Matsuda, S. Terashima, M. Kawasaki, 1988 .

Total syntheses of (+)-nogarene and (+)-7,8-dihydronogarene

F. Matsuda, S. Terashima, M. Kawasaki, 1986 .

Stereochemical Studies. XXXIX. A Novel Method for the Preparation of Optically Active Aldehydes. Syntheses of Optically Active (R) (+)-α-Cyclocitral, (S) (+)-Dehydrovomifoliol, and (S) (+)-Abscisic Acid

M. Shibasaki, S. Terashima, S. Yamada, 1976 .

Stereochemical Studies. XXXV. A Biogenetic-type Asymmetric Cyclization. Syntheses of optically Active α-Cyclocitral and trans-α-Damascone

M. Shibasaki, S. Terashima, S. Yamada, 1975 .

Synthetic studies on himbacine, a potent antagonist of the muscarinic M2 subtype receptor. Part 2: synthesis and muscarinic M2 subtype antagonistic activity of the novel himbacine congeners modified at the C-3 position of lactone moiety.

S. Terashima, K. Yamaguchi, M. Takadoi, 2003, Bioorganic & medicinal chemistry.

Synthesis and muscarinic M(2) subtype antagonistic activity of enantiomeric pairs of 3-demethylhimbacine (3-norhimbacine) and its C(4)-epimer.

S. Terashima, K. Yamaguchi, M. Takadoi, 2002, Bioorganic & medicinal chemistry letters.

A NOVEL TOTAL SYNTHESIS OF (+)-HIMBACINE, A POTENT ANTAGONIST OF THE MUSCARINIC RECEPTOR OF M2 SUBTYPE

T. Katoh, S. Terashima, A. Ishiwata, 1999 .

Synthesis and optical resolution of dl-cis-2-fluorocycloproplylamine, the key component of the new generation of quinolonecarboxylic acid, DU-6859

K. Nakatani, Yuko Kobayashi, T. Katoh, 1992 .

Absolute Configuration of Biochemically Active (-)-α-Methyl-3, 4-dihydroxyphenylalanine

K. Achiwa, S. Terashima, S. Yamada, 1965 .

Novel Glycosidation of 4-Demethoxyanthracyclinones by the Use of Trimethylsilyl Triflate. Syntheses of Optically Active 4-Demethoxydaunorubicin and 4-Demethoxyadriamycin

Y. Kimura, S. Terashima, R. Abe, 1986 .

Total syntheses of natural (+)-sesbanimide A and (−)-sesbanimide B

F. Matsuda, S. Terashima, 1986 .

Syntheses and Cytotoxicity of the AB-, C-, and BC-Ring Systems of Sesbanimides

F. Matsuda, S. Terashima, Kaoru Yamada, 1988 .

Synthetic studies of carzinophilin. Part 1: Synthesis of 2-methylidene-1-azabicyclo[3.1.0]hexane systems related to carzinophilin

S. Terashima, M. Hashimoto, M. Matsumoto, 2003 .

Total Synthesis of Sesbanimides

F. Matsuda, S. Terashima, 1988 .

Syntheses and Cytotoxicity of the AB-, C-, and BC-Ring Systems of Sesbanimides.

F. Matsuda, S. Terashima, Kaoru Yamada, 1988 .

Novel Synthesis of Three Types of C-Terminal Components of Renin Inhibitors from Unnatural (2S,3S)-Tartaric Acid

K. Nakatani, Yuko Kobayashi, S. Terashima, 1991 .

Synthesis of various model compounds for the conjugated heterocyclic ring system of antibiotic roseophilin

S. Terashima, S. Nakatani, Kaoru Yamada, 1995 .

Total Synthesis of Antitumor Antibiotic FR900482

T. Katoh, S. Terashima, 1997 .

A novel synthesis of (±)-2-acetyl-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol, a key intermediate for the synthesis of anthracyclinones

K. Koga, S. Terashima, N. Tanno, 1980 .

An Expeditious Synthesis of the (2R,3S)- and (2S,3R)-3-Amino-2-hydroxycarboxylic Acids, the Key Components of a Renin Inhibitor and Bestatin, from (S)- and (R)-Phenylalanine

F. Matsuda, S. Terashima, Yoshio N Ito, 1990 .

Total synthesis of natural (+)-sesbanimide a and (-)-sesbanimide b

F. Matsuda, S. Terashima, 1988 .

Studies toward the total synthesis of antibiotic roseophilin: A novel synthesis of the macrotricyclic part

T. Katoh, S. Terashima, N. Shibata, 1998 .

Synthesis of Various Model Compounds for the Conjugated Heterocyclic Ring System of Antibiotic Roseophilin.

S. Terashima, S. Nakatani, M. Kirihara, 1996 .

An expeditious synthesis of (2R,3S)-3-tert-butoxycarbonylamino-1-isobutylamino-4-phenyl-2-butanol, a key building block of HIV protease inhibitors

T. Katoh, S. Terashima, N. Shibata, 1997 .

Total synthesis of an enantiomeric pair of FR900482. 3. Completion of the synthesis by assembling the two segments

T. Katoh, S. Terashima, T. Yoshino, 1997 .

Asymmetric Halolactonization Reactions. 3. Asymmetric Synthesis of optically Active Anthracyclinones

K. Koga, S. Terashima, S. Jew, 1979 .

Novel use of -compound for the preparation of optically active compounds: synthesis of optically active prostaglandin intermediates from -2-cyclopentene-1,4-diol

S. Terashima, S. Yamada, Nara Munehiko, 1977 .

An Expeditious Synthesis of the (2R,3S)- and (2S,3R)-3-Amino-2-hydroxycarboxylic Acids (VI) and (X), the Key Components of a Renin Inhibitor and Bestatin, from (S)- and (R)-Phenylalanine.

F. Matsuda, S. Terashima, Yoshio N Ito, 2010 .

Stereochemical Studies. III. Chemical Correlation of Absolute Configuration of 2-Cyano-2-methyl-3-phenylpropionic Acid to α-Methyl-α-isopropylsuccinic Acid

S. Terashima, S. Yamada, Kongko Lee, 1969 .

A novel synthesis of the C1–C17 fragment of carzinophilin

S. Terashima, M. Hashimoto, 1994 .

Synthesis and acetylcholinesterase inhibitory activity of fluorinated analogues of huperzine A

N. Nakajima, T. Katoh, S. Terashima, 1996 .

Synthesis and Acetylcholinesterase Inhibitory Activity of Fluorinated Analogues of Huperzine A.

N. Nakajima, T. Katoh, S. Terashima, 1996 .

Synthetic studies on quinocarcin and its related compounds. 5.

K. Nakatani, T. Ashizawa, F. Matsuda, 1994 .

A Practical Synthesis of threo-3-Amino-2-hydroxycarboxylic Acids.

F. Matsuda, S. Terashima, Yoshio N Ito, 1992 .

An Enantioselective Synthesis of Natural (-)-Huperzine A via Cinchona Alkaloid Promoted Asymmetric Michael Reaction.

T. Katoh, S. Terashima, T. Yoshino, 1998 .

AN ENANTIOSELECTIVE SYNTHESIS OF NATURAL (-)-HUPERZINE A VIA CINCHONA ALKALOIDS-PROMOTED ASYMMETRIC MICHAEL REACTIONS

T. Katoh, S. Terashima, T. Yoshino, 1997 .

An expeditious synthesis of the open-chain (E)- and (Z)–dienediyne systems related to neocarzinostatine chromophore

K. Nakatani, S. Terashima, Kaoru Yamada, 1991 .

An Expeditious Synthesis of the Open-Chain E- and Z-Dienediyne Systems Related to Neocarzinostatine Chromophore.

K. Nakatani, S. Terashima, Kaoru Yamada, 1992 .

Synthesis and cytotoxicity of the acyclic (E)- and (Z)-dienediyne systems related to neocarzinostatine chromophore

K. Nakatani, F. Matsuda, S. Terashima, 1990 .

Regioselective intramolecular asymmetric cyclization of symmetrical open chain triketone

K. Koga, S. Terashima, Susumu Sato, 1980 .

Trimethylsilyl trifluoromethanesulfonate (trimethylsilyl triflate) as an excellent glycosidation reagent for anthracycline synthesis: simple and efficient synthesis of optically pure 4-demethoxydaunorubicin

Y. Kimura, S. Terashima, R. Abe, 1984 .

A novel synthesis of the 2-aminoimidazol-4-carbaldehyde derivatives, versatile synthetic intermediates for 2-aminoimidazole alkaloids

S. Terashima, N. Ando, 2006 .

Efficient synthesis and biological activity of enantiomeric pairs of thiolactomycin and its 3-demethyl derivative

S. Terashima, Kohei Ohata, 2009 .

Synthesis and biological activity of enantiomeric pairs of 5-[(E)-cycloalk-2-enylidenemethyl]thiolactomycin congeners.

S. Terashima, Kohei Ohata, 2008, Bioorganic & medicinal chemistry letters.

Synthesis and biological activity of enantiomeric pairs of 5-vinylthiolactomycin congeners.

S. Terashima, Kohei Ohata, 2007, Bioorganic & medicinal chemistry letters.

Efficient synthesis of enantiomeric pairs of thiolactomycin and its 3-demethyl derivative

S. Terashima, Kohei Ohata, 2006 .

Synthesis and biological activity of enantiomeric pairs of 5-(Alk-2-enyl)thiolactomycin and 5-[(E)-Cycloalk-2-enylidenemethyl]thiolactomycin congeners.

S. Terashima, Kohei Ohata, 2009, Chemical & pharmaceutical bulletin.

Studies on optically Active Amino Acids. XVIII. Studies on α-Methyl-α-amino Acids. XIV. Several Optical Properties of α-Methyl-α-amino Acids

K. Achiwa, S. Terashima, N. Takamura, 1970 .

Study of the cluster state at Ex=10.3 MeV in 12C

H. Sakaguchi, T. Kawabata, M. Uchida, 2004 .

Evidence for an alpha cluster condensed state in 16O(alpha,alpha') at 400 MeV

H. Sakaguchi, Y. Shimizu, M. Uchida, 2006 .

Novel efficient synthesis of an enantiomeric pair of tricycloillicinone

S. Terashima, Sanae Furuya, 2003 .

Novel Efficient Synthesis of an Enantiomeric Pair of Tricycloillicinone.

S. Terashima, Sanae Furuya, 2003 .

Synthetic studies of carzinophilin. Part 4: Chemical and biological properties of carzinophilin analogues

S. Terashima, M. Hashimoto, Kaoru Yamada, 2003 .

Synthesis, Chemical Reactivity, and Cytotoxicity of 2-Bis(alkoxycarbonyl)methyliden-1-azabicyclo[3.1.0]hexane Systems Related to Antitumor Antibiotic Carzinophilin A

S. Terashima, M. Hashimoto, Kaoru Yamada, 1992 .

Novel synthesis of (+)-hydantocidin based on the plausible biosynthetic pathway

N. Nakajima, T. Katoh, S. Terashima, 1996 .

Asymmetric reduction of 4-phenyl-3(E)-buten-2-one by using lithium aluminum hydride partially decomposed with (-)-N-methylephedrine and achiral secondary amine.

S. Terashima, M. Kawasaki, 1985 .

ASYMMETRIC REDUCTION OF 4-PHENYL-3(E)-BUTEN-2-ONE BY USING LITHIUM ALUMINUM HYDRIDE PARTIALLY DECOMPOSED WITH (-)-N-METHYLEPHEDRINE AND ACHIRAL SECONDARY AMINE

S. Terashima, M. Kawasaki, 1985 .

A Novel Synthetic Approach to 2,2,2-Trifluoroethylidene Derivatives from Ketones.

N. Nakajima, T. Katoh, S. Terashima, 1997 .

Studies on Optically Active Amino Acids. IX. Studies on α-Alkyl-α-amino Acids. IV. Chemical Correlation of Absolute Configuration of α-Methylaspartic Acid to Isovaline

K. Achiwa, S. Terashima, S. Yamada, 1966 .

14-Fluoroanthracyclines. Novel syntheses and antitumor activity.

F. Matsuda, S. Terashima, T. Matsumoto, 1988, Chemical & pharmaceutical bulletin.

Efficient synthesis and antitumor activity of novel 14-fluoroanthracyclines

F. Matsuda, S. Terashima, M. Ohsaki, 1987 .

Stereochemical studies-LVIII

S. Terashima, S. Yamada, M. Nara, 1980 .

Synthesis of optically pure steroid intermediate by the novel use of meso-compound

S. Terashima, S. Yamada, Nara Munehiko, 1978 .

Application of Successive Cleavage and Formation, or vice versa, of Cyclic Compound to Natural Product Synthesis, Its Recent Development

S. Terashima, 1977 .

Amino Acids and Peptides. I. Novel Peptide Bond Formation Catalyzed by Metal Ions. I. Formation of Glycine Peptide Esters

S. Terashima, Y. Takéuchi, M. Wagatsuma, 1971 .

Stereochemical studies. XLII. Asymmetric synthesis of naturally occurring podocarpic acid.

S. Terashima, T. Sone, S. Yamada, 1976 .

A biogenetic-type asymmetric cyclization syntheses of optically active α-cyclocitral and trans-α-damascone

M. Shibasaki, S. Terashima, S. Yamada, 1973 .

Stereochemical Studies. II. Thermal and Photochemical Decompositions of Optically Active Alkyl Azidoformates

S. Terashima, S. Yamada, 1968 .

Cluster fragmentations of deep(1s)-hole states in light nuclei

E. Obayashi, H. Sakaguchi, T. Kawabata, 2004 .

Synthesis of (±)-12-Fluorohuperzine A, a Novel Acetylcholinesterase Inhibitor

T. Katoh, S. Terashima, M. Shikano, 1997 .

Studies on Optically Active Amino Acids. VI. Studies on α-Alkyl-α-amino Acids. II. Resolution of Some α-Methyl-α-amino Acids through l-Menthyl Ester

K. Achiwa, S. Terashima, S. Yamada, 1965 .

Asymmetric Reduction of Various Types of Ketones with Lithium Aluminum Hydride partially decomposed with (-)-N-Methylephedrine and N-Ethylaniline

S. Terashima, N. Tanno, 1983 .

(ACETYLACETONATO)((-)-N-ALKYLEPHEDRINATO)DIOXOMOLYBDENUM, A NEW CLASS OF CHIRAL CHELATE COMPLEXES WHICH CATALYZE ASYMMETRIC EPOXIDATION OF ALLYLIC ALCOHOL

S. Terashima, T. Mashiko, S. Yamada, 1977 .

A Stereoselective Synthesis of 4-O-Methyl- 13-desacetyl-12,13-di-O-benzylcarzinophilin

S. Terashima, M. Hashimoto, 1998 .

A Novel Synthesis of the (2R,3S)‐ and (2S,3R)‐3‐Amino‐2‐ hydroxycarboxylic Acid Derivatives, the Key Components of a Renin Inhibitor, and Bestatin, from Methyl (R)‐ and (S)‐Mandelate.

Yuko Kobayashi, S. Terashima, Y. Takemoto, 1991 .

Asymmetric synthesis of optically pure (R)(−)-2-acetyl-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol, a key intermediate for optically active anthracyclinone synthesis

K. Koga, S. Terashima, N. Tanno, 1980 .