T. Momose

发表

A short, chirospecific synthesis of the ant venom alkaloid (3R,5S,8S)-3,5-dialkylpyrrolizidines

H. Takahata, H. Bandoh, T. Momose, 1992 .

Concise Syntheses of Natural .gamma.-Butyrolactones, (+)-trans-Whisky Lactone, (+)-trans-Cognac Lactone, (-)-Methylenolactocin, (+)-Nephrosteranic Acid, and (+)-Roccellaric Acid Using Novel Chiral Butenolide Synthons

H. Takahata, T. Momose, Y. Uchida, 1995 .

1, 6-Dihydro-3 (2H)-pyridinones. II. Synthesis of 2-Azabicyclo [2. 2. 2] octanes by the Reaction of N-Substituted 1, 6-Dihydro-3 (2H)-pyridinones with 1, 3-Dicarbonyl Compounds

T. Imanishi, M. Hanaoka, T. Momose, 1982 .

Synthetic Studies on Anthracyclinones. IX. Lithiation of N, N-Dimethylnaphthalenemethylamines and a New Synthetic Pathway to 2, 3-Naphthalides

T. Momose, Z. Horii, Y. Matsumoto, 1971 .

3-Hydroxypyrroles. III. Synthesis and Tautomerism of N-Alkyl-3-hydroxypyrroles

Tetsuaki Tanaka, T. Yokota, T. Momose, 1979 .

Asymmetric twin-ring differentiation by lipase-catalyzed enantiotoposelective reaction of the ring-crossed meso glycol: Asymmetric synthesis of a highly functionalized piperidine from the conjoined twin piperidine system

N. Toyooka, T. Momose, M. Jin, 1992 .

An asymmetric total synthesis of (−)-supinidine

H. Takahata, T. Momose, Y. Banba, 1991 .

Asymmetric intramolecular amidation of N-(tert-butoxycarbonyl)-3-hydroxy-4-pentenylamine. A new entry to chiral building blocks for the synthesis of biologically active nitrogen-containing compounds

May Tajima, H. Takahata, T. Momose, 1991 .

The Structures of Securinol B and C

M. Yamauchi, T. Momose, M. Ikeda, 1970 .

Enantio- and diastereodivergent synthesis of all four diastereomers of the 2,6-disubstituted 3-piperidinol chiral building block

N. Toyooka, T. Momose, Yasuko Yoshida, 1995 .

Chapter 3 Simple Indolizidine Alkaloids

H. Takahata, T. Momose, 1993 .

Bicyclo[3.3.1]nonanes as Synthetic Intermediates. XXIII.1 A Breakthrough by Lanthanoid Mediation in Nucleophilic Addition of Carbanions to the Inert “Fork Head” Carbonyl in Bicyclo[3.3.1]nonan-3-ones

S. Takizawa, T. Momose, M. Kirihara, 1997 .

A Facile Synthesis of 7-Methylenebicyclo-[3.3.1]nonan-3-one and its Transformation Leading to the Novel Tricyclic System, Protoadamantane

G. Tanabe, O. Muraoka, Ya-lou Wang, 1996 .

4-Oxo-2-pyrrolines Carrying No Substituents on the Ring Carbon: Substituent Effects in the Tautomerism between 4-Oxo-2-pyrrolines and 3-Hydroxypyrroles

Tetsuaki Tanaka, T. Yokota, T. Momose, 1977 .

Indium-Mediated Reaction of 3-Bromo-3,3-difluoropropene and Bromodifluoromethylacetylene Derivatives with Aldehydes

S. Takizawa, H. Nemoto, T. Takuwa, 2000 .

The norrish type I photo-cleavage of (+)-2β-ethyl-9-azabicyclo[3.3.1]nonan-3-one: A short, enantioselective formal synthesis of (−)-Indolizidine 223ab

G. Tanabe, O. Muraoka, Tomomi Maeda, 1994 .

ASYMMETRIC SYNTHESIS OF INDOLIZIDINES 167B AND 223AB

H. Takahata, H. Bandoh, T. Momose, 1995 .

A short, practical synthesis of the ant venom alkaloid, three (3R,5S,8aS)-3-alkyl-5-methylindolizidines

H. Takahata, H. Bandoh, T. Momose, 1993 .

A new asymmetric entry to 2-substituted piperidines. A concise synthesis of (+)-coniine, (−)-pelletierine, (+)-δ-coniceine, and (+)-epidihydropinidine

H. Takahata, T. Momose, M. Kubota, 1996 .

Synthetic Studies on Anthracyclinones. VII. Synthesis of Bisanhydroaklavinone

H. Hakusui, T. Momose, Z. Horii, 1968 .

New synthesis of all the four stereoisomers of indolizidine 209D and their affinity for nicotinic acetylcholine receptor

A. Eldefrawi, M. Eldefrawi, H. Takahata, 1998 .

Highly stereoselective construction of trans(2,3)-cis(2,6)-trisubstituted piperidines: An application to the chiral synthesis of Dendrobates alkaloids

J. Daly, N. Toyooka, H. M. Garraffo, 1997 .

Bicyclo[3.3.1]nonanes as synthetic intermediates. Part 20.1 Asymmetric synthesis of the indolizidine alkaloids monomorine I and indolizidine 223AB

N. Toyooka, T. Momose, Y. Hirai, 1997 .

A general asymmetric route to trans- or cis-2,6-disubstituted piperidine. First total synthesis of (+)-9-epi-6-epipinidinol and (−)-pinidinol

H. Takahata, T. Momose, Yasuhito Yotsui, 1998 .

Bicyclo[3.3.1]nonanes as synthetic intermediates. Part 19.1 Asymmetric cleavage of ω-azabicyclo[3.n.1]alkan-3-ones at the ‘fork head’

C. Eugster, N. Toyooka, T. Momose, 1997 .

Asymmetric Synthesis of Indolizidines 167B and 223 AB.

H. Takahata, H. Bandoh, T. Momose, 1995 .

New entry to chiral butenolide synthons. Application to expeditious syntheses of (+)-nephrosteranic acid, (+)-trans-whisky lactone, and (+)-trans-cognac lactone

H. Takahata, T. Momose, Y. Uchida, 1994 .

A novel approach to (+)-yohimbine

Y. Okaji, T. Yamazaki, T. Momose, 1990 .

AN ASYMMETRIC SYNTHESIS OF THE ANT VENOM ALKALOID (3S,5S,8AR)-3-BUTYL-5-(4-PENTENYL)INDOLIZIDINE VIA THE SHARPLESS ASYMMETRIC DIHYDROXYLATION

H. Takahata, H. Bandoh, T. Momose, 1996 .

2-Piperidone Type of Chiral Building Block for 3-Piperidinol Alkaloid Synthesis.

N. Toyooka, T. Momose, Yasuko Yoshida, 1999, The Journal of organic chemistry.

Heterocycles in asymmetric synthesis. Part 1. Construction of the chiral building blocks for enantioselective alkaloid synthesis via an asymmetric intramolecular Michael reaction

T. Yamazaki, T. Momose, Y. Hirai, 1992 .

SYMMETRY-ASSISTED SYNTHESIS OF C2-SYMMETRIC TRANS-ALPHA , ALPHA '-BIS(HYDROXYMETHYL)PYRROLIDINE AND -PIPERIDINE DERIVATIVES VIA DOUBLE SHARPLESS ASYMM ETRIC DIHYDROXYLATION OF ALPHA , OMEGA -TERMINAL DIENES

H. Takahata, T. Momose, Shinji Kouno, 1998 .

Synthetic Studies on η-Pyrromycinone. V. Total Synthesis of η-Pyrromycinone

Y. Tamura, T. Momose, Z. Horii, 1965 .

2(3H)- and 2(5H)-Furanones. IV. The Di-π-methane Rearrangement of 3, 4-Bis(phenymethyl)-2(5H)-furanone

G. Tanabe, O. Muraoka, T. Momose, 1992 .

Synthesis of natural (S)-(−)-tulipalin B starting from L-malic acid as a chiral pool

O. Muraoka, N. Toyooka, T. Momose, 1989 .

A breakthrough for the photochemical arylation in the 3-(phenylmethyl)-2(5H)-furanone system leading to the tetrahydroindenofuranone system

G. Tanabe, O. Muraoka, T. Momose, 1992 .

Accentuation of the Di-p-Methane Reactivity by Central Carbon Substitution in the 4-(Phenylmethyl)-2(5H)-furanone System

G. Tanabe, O. Muraoka, T. Momose, 1990 .

The Di-p-methane Rearrangement in 3,4-Dibenzyl-2(5H)-furanone

G. Tanabe, K. Kanai, T. Momose, 1989 .

Synthetic Studies on Lignans and Related Compounds. VI. Photochemical Rearrangement of β-Apolignans

K. Kanai, T. Momose, Takeshi Nakamura, 1978 .

Efficient fragmentation of the tertiary cyclopropanol system: Oxidation of 1-(trimethylsiloxy)bicyclo[n.1.0]alkanes and analogues by using phenyliodine(III) diacetate

T. Momose, H. Kakuda, S. Yokoyama, 1995 .

Tertiary cyclopropanol systems as synthetic intermediates: novel ring-cleavage of tertiary cyclopropanol systems using vanadyl acetylacetonate

S. Takizawa, T. Momose, M. Kirihara, 1998 .

Allylic fluorides via the cleavage of tertiary cyclopropyl silyl ethers with diethlaminosulfur trifluoride

T. Momose, M. Kirihara, T. Kambayashi, 1996 .

Functionalized chiral γ-butyrolactones as C5 building units: a straightforward formal synthesis of (+)- exo- and (+)-endo-brevicomines

H. Takahata, T. Momose, M. Kusunoki, 1996 .

A chirospecific synthesis of (−)-pinidine

H. Takahata, H. Bandoh, T. Momose, 1992 .

An efficient route to chiral trans-2,5-dialkylpyrrolidines via stereoselective intramolecular amidomercuration

H. Takahata, T. Momose, H. Takehara, 1990 .

Hypervalent λn-iodane-mediated fragmentation of tertiary cyclopropanol systems II: Application to asymmetric syntheses of piperidine and indolizidine alkaloids

T. Nishio, T. Momose, H. Kakuda, 1999 .

Hypervalent λn-iodane-mediated fragmentation of tertiary cyclopropanol systems

T. Momose, H. Kakuda, S. Yokoyama, 1998 .

A Significant Effect of Triflic Acid on the Hypervalent λn-Iodane-Mediated Fragmentation of the Tertiary Cyclopropanol System

T. Momose, S. Yokoyama, M. Kirihara, 1998 .

Synthetic Studies on Lignans and Related Compounds. VIII. : Synthesis of Justicidin B and Diphyllin and of Taiwanin C and E from 2, 3-Dibenzylidenebutyrolactones via β-Apolignans : A Chemical Model for Natural Co-occurrence of 4-Hydrogen-and 4-Hydroxy-1-phenyl-2, 3-naphthalides in Plants

K. Kanai, T. Momose, K. Hayashi, 1978 .

Synthetic Studies on Lignans and Related Compounds. V. Regiospecificity in the Photocyclization of 2,3-Dibenzylidenebutyrolactones

K. Kanai, T. Momose, Takeshi Nakamura, 1977 .

a-Allylation of b-Tetronic Acids and Chirality Transfer via the 4-Oxygenated 2(5H)-Furanone System

N. Toyooka, T. Momose, Hiromi Fujii, 1989 .

A Short, Practical Synthesis of the Ant Venom Alkaloid, Three (3R,5S, 8aS)-3-Alkyl-5-methylindolizidines.

H. Takahata, H. Bandoh, T. Momose, 1994 .

An asymmetric synthesis of an acetonide form of (−)-cis-1,2-dihydroxyindolizidine

H. Takahata, T. Momose, Y. Banba, 1992 .

TOTAL SYNTHESIS OF (+)-MONOMORINE I VIA ASYMMETRIC α-KETONIC CLEAVAGE OF 8-AZABICYCLO[3.2.1]OCTAN-3-ONE

N. Toyooka, T. Momose, Y. Hirai, 1990 .

A facile synthesis of N-protected statine and its analog via stereoselective iodolactamization

T. Yamazaki, H. Takahata, T. Momose, 1990 .

Electrophilic olefin heterocyclization in organic synthesis. Highly stereoselective synthesis of trans 3,5-disubstituted pyrrolidin-2-ones by iodolactamization via homoallylic asymmetric induction

T. Yamazaki, H. Takahata, T. Momose, 1990 .

α,α-difluoroallyl carbanion: Indium-mediation in its facile coupling with aldehydes

S. Takizawa, T. Takuwa, T. Momose, 1997 .

Bicyclo[3.3.1]nonanes as synthetic intermediates XIII. : Novel transannular hydride shifts enforced by relief of the steric constraint in the bicyclo[3.3.1]nonane system bearing endo-substituents at position 7

O. Muraoka, Mari L. Uchimoto, T. Momose, 1987 .

Bicyclo [3.3.1] nonanes as Synthetic Intermediates. I. Improved Synthetic Methods for Bicyclo [3.3.1] nonan-3-one

O. Muraoka, T. Momose, 1978 .

Efficient synthesis of an enantiomeric pair pinpinidine: An illustration of organochemical carving on the rigid bridged system as the stereochemical tactics

T. Nishio, T. Momose, M. Kirihara, 1996 .

High-Enantioselective Synthesis of Pyrrolidine Derivatives as Chiral Building Blocks

T. Yamazaki, T. Momose, Y. Hirai, 1989 .

2(3H)- and 2(5H)-Furanones. III: An efficient synthesis and the Eschenmoser-Mannich reaction of N-substituted 4-amino-2(5H)-furanones

N. Toyooka, T. Momose, Takafumi Nishi, 1988 .

Studies on oxytetracycline and related compounds. XVII. Synthesis of 1,3,11-trimethoxynaphthacenequinone.

Y. Tamura, T. Momose, Z. Horii, 1962, Chemical & pharmaceutical bulletin.

A GENERAL ENTRY TO 2-(2-HYDROXYALKYL)PIPERIDINES VIA ITERATIVE ASYMMETRIC DIHYDROXYLATION TO CAUSE ENANTIOMERIC ENHANCEMENT

H. Takahata, T. Momose, M. Kubota, 1997 .

A New Asymmetric Entry to 2‐Substituted Piperidines. A Concise Synthesis of (+)‐Coniine (VIII), (‐)‐Pelletierine (IX), (+)‐δ‐ Coniceine (XI), and (+)‐Epidihydropinidine (XIII).

H. Takahata, T. Momose, M. Kubota, 1997 .

A New Procedure for Construction of 2,6-trans-Disubstituted Piperidines Using Osmium-catalyzed Asymmetric Dihydroxylation: Application to the Synthesis of (+)-Epidihydropinidine and (+)-Solenopsin A1

H. Takahata, T. Momose, Kumiko Inose, 1994 .

Octahydro-7(1H)-quinolones. I. Stereochemistries of catalytic hydrogenation of 7-hydroxyquinoline.

T. Imanishi, T. Momose, S. Uchida, 1977 .

On the Dual Mode of Aldol Cyclization of Bicyclo-[4.3.1]Decane-3,8-Dione: A Novel, Efficient Entry into the Isotwistanone System

O. Muraoka, T. Momose, T. Itooka, 1982 .

Bicyclo [3. 3. 1] nonanes as Synthetic Intermediates. II. Synthesis of Bicyclo [3. n. 1] alkan-3-one via α, α'Annelation of Cycloalkanone

O. Muraoka, T. Momose, 1978 .

On the transannular cyclization of 3,7-difunctionalized bicyclo[3.3.1]nonanes: revision of the literature

O. Muraoka, T. Momose, 1978 .

Novel steric factors operating on the baeyer-villiger oxidation of bicyclo[3,3,1]Nonan-3-one system

O. Muraoka, T. Momose, S. Atarashi, 1974 .

Aerobic deprotection of monothioacetals catalyzed by trichlorooxyvanadium

S. Takizawa, Yuta Ochiai, H. Nemoto, 1999 .

Highly chemoselective, oxyvanadium-catalysed cleavage of α-hydroxy ketones

S. Takizawa, T. Momose, M. Kirihara, 1998 .

Transesterification-based enzymatic resolutions of racemic 3-hydroxy-4-pentenylurethanes in organic solvents

H. Takahata, T. Momose, Y. Uchida, 1992 .

New entry to C2 symmetric trans-2,6-bis(hydroxymethyl)-piperidine derivatives via the Sharpless asymmetric dihydroxylation

H. Takahata, T. Momose, Shinji Kouno, 1995 .

Asymmetric synthesis of the indolizidine alkaloids 207A, 209B, and 235B' : 6-substituted 2,3-didehydropiperidine-2-carboxylate as a versatile chiral building block

N. Toyooka, T. Momose, 1994 .

An efficient synthesis of (-)-bulgecinine

T. Momose, Y. Hirai, T. Terada, 1992 .

Asymmetric cleavage of 9-azabicyclo[3.3.1]nonan-3-one into cis-2,6-disubstituted piperidine. A facile approach to a chiral building block for alkaloid synthesis

N. Toyooka, T. Momose, Y. Hirai, 1990 .

Bicyclo[3.3.1]nonanes as synthetic intermediates. Part 21.1 Enantiodivergent synthesis of the cis,cis 2,6-disubstituted piperidin-3-ol chiral building block for alkaloid synthesis

N. Toyooka, T. Momose, M. Jin, 1997 .

Asymmetric synthesis of the alkaloid 2,6-disubstituted piperidin-3-ols, (-)-cassine and (+)-spectaline

N. Toyooka, T. Momose, 1993 .

Asymmetric Synthesis of the Alkaloid 2,6-Disubstituted Piperidin-3-ols, (-)Cassine (I), and (+)-Spectaline (II).

N. Toyooka, T. Momose, 1993 .

Bicyclo(3.3.1)nonanes as Synthetic Intermediates. Part 21. Enantiodivergent Synthesis of the cis,cis 2,6-Disubstituted Piperidin- 3-ol Chiral Building Block for Alkaloid Synthesis.

N. Toyooka, T. Momose, M. Jin, 2010 .

Highly stereoselective construction of 4,6-cis-substituted quinolizidine ring core: an application to enantioselective total synthesis of the marine alkaloid clavepictines A, B and pictamine

N. Toyooka, H. Nemoto, T. Momose, 1999 .

Enantioselective Total Synthesis of the Marine Alkaloid Clavepictines A and B

N. Toyooka, T. Momose, Yasuhito Yotsui, 1996 .

A short and practical synthesis of (+)-pseudoconhydrine and (+)-N-methylpseudoconhydrine via osmium catalyzed asymmetric dihydroxylation

H. Takahata, T. Momose, Kumiko Inose, 1994 .

The shortest synthesis of optically active Geissman-Waiss lactone, a key synthetic intermediate for necine bases

H. Takahata, T. Momose, Y. Banba, 1991 .

Asymmetric Synthesis of Methyl N,O-Diacetylspicigerinate

N. Toyooka, T. Momose, 1995 .

Enantioselective Total Synthesis of the Marine Alkaloid Clavepictines A (XI) and B (IX).

N. Toyooka, T. Momose, Yasuko Yoshida, 1996 .

Highly Stereoselective Construction of 4,6-cis-Substituted Quinolizidine Ring Core: An Application to Enantioselective Total Synthesis of the Marine Alkaloid Clavepictines A (Va), B (IIIa) and Pictamine (Vb).

N. Toyooka, H. Nemoto, T. Momose, 2000 .

Tandem Beckmann and Huisgen–White rearrangement as an alternative to the Baeyer–Villiger oxidation of the bicyclo[3.3.1]nonane system: first asymmetric synthesis of (–)-dihydropalustramic acid. X-Ray molecular structure of 2β-ethyl-9-phenylsulfonyl-9-azabicyclo[3.3.1]nonan-3-one

C. Eugster, G. Tanabe, O. Muraoka, 1996 .

A Short and Practical Synthesis of (+)-Pseudoconhydrine and (+)-N- Methylpseudoconhydrine via Osmium-Catalyzed Asymmetric Dihydroxylation.

H. Takahata, T. Momose, Kumiko Inose, 1994 .

The Shortest Synthesis of Optically Active Geissman‐Waiss Lactone, a Key Synthetic Intermediate for Necine Bases.

H. Takahata, T. Momose, Y. Banba, 1991 .

ELECTROPHILIC OLEFIN HETEROCYCLIZATION IN ORGANIC SYNTHESIS. : STEREOSELECTIVE INTRAMOLECULAR AMIDOMERCURATION OF γ-HYDROXY-δ, ε-UNSATURATED URETHANES

May Tajima, H. Takahata, T. Momose, 1989 .

3-Hydroxypyrroles. I. A General Synthetic Route to 4,5-Unsubstituted Alkyl 3-Hydroxypyrrole-2-carboxylates

Tetsuaki Tanaka, T. Yokota, T. Momose, 1978 .

Studies on the Novel Cyclodepsipeptides. A Total Synthesis of (+)-Jasplakinolide (Jaspamide)

T. Momose, Y. Hirai, K. Yokota, 1994 .

Asymmetric Construction of Versatile Chiral Building Blocks and Their Application to the Syntheses of Natural Products

T. Momose, Y. Hirai, 2010 .

Heterocycles in asymmetric synthesis. Part 2. Efficient asymmetric approaches to heteroyohimbine, yohimbine and related alkaloids

T. Yamazaki, T. Momose, Y. Hirai, 1992 .

An enantioselective construction of pyrrolidones bearing functionalized appendages via an asymmetric intra-molecular Michael reaction

S. Sonohara, T. Momose, Y. Hirai, 1991 .

Asymmetric synthesis of 1-hydroxyindolizidines, biosynthetic precursors to the toxic indolizidine alkaloids slaframine and swainsonine

H. Takahata, T. Momose, Y. Banba, 1990 .

Bicyclo[3.3.1] Nonanes as Synthetic Intermediates. Viii.1 1-Alkoxybicyclo [4.3.1] Decan-3-Onecarboxylates via the Anti-Bredt [4.3.1] System: An Improved Synthetic Route to Bicyclo [4.3.1] Decan-8-One

O. Muraoka, T. Momose, K. Masuda, 1984 .

Alpha-bromo-alpha,alpha-difluoroallyl derivatives as synthetic intermediate: nucleophilic substitution of alpha-bromo-alpha,alpha-difluoroallyl derivatives in the presence of palladium catalysts.

Y. Takéuchi, H. Nemoto, T. Takuwa, 2000, Chemical & pharmaceutical bulletin.

Bicyclo[3.3.1]Nonanes as Synthetic Intermediates. Vii.(1) An Intramolecular Alkylation in the Bicyclo[3.3.1]nonan-3-One System by the “fork head” endo-Methanol: An Efficient Route to 4-Protoadamantanone

O. Muraoka, T. Momose, T. Itooka, 1984 .

Synthetic Studies on Anthracyclinones. VI. The Friedel-Crafts Condensation between 3-Methoxyphthalic Anhydride and α-Naphthol Derivatives

H. Hakusui, T. Momose, Z. Horii, 1968 .

Bicyclo [3. 3. 1] nonanes as Synthetic Intermediates. IX. Photo-Irradiation of Bicyclo [3....1] alkan-3-one in Cyclohexane : A Selective Photo-Reduction with Predominance of endo-Hydrogenation

O. Muraoka, T. Momose, K. Masuda, 1984 .

Synthesis of bisanhydroaklavinone.

H. Hakusui, T. Momose, Z. Horii, 1966, Chemical & pharmaceutical bulletin.

SYNTHESIS OF METHYL 2-ETHYL-6,11-DIOXO-5,7,10-TRIMETHOXY-6,11-DIHYDRO-1-NAPHTHACENECARBOXYLATE (ETA-PYRROMYCINONE TRIMETHYL ETHER).

Y. Tamura, T. Momose, Z. Horii, 1964, Chemical & pharmaceutical bulletin.

Furan-2(3H)- and 2(5H)-ones. Part 5. Photoreactions of 3-benzylfuran2(5H)-ones; cyclisation to indenofuranones

G. Tanabe, O. Muraoka, T. Momose, 1994 .

Furan‐2(3H)‐ and 2(5H)‐ones. Part 5. Photoreactions of 3‐Benzylfuran‐2( 5H)‐ones: Cyclization to Indenofuranones.

G. Tanabe, O. Muraoka, T. Momose, 1994 .

Furan-2(3H)- and -2(5H)-ones. Part 6. Di-π-methane rearrangement of the α-substituted 4-benzylfuran-2(5H)-one system

G. Tanabe, O. Muraoka, T. Momose, 1995 .

Synthesis of N-Substituted 1,6-Dihydro-3 (2H)-Pyridi-None. The Simplest Azacyclic α-Enone Lacking Conjugation with Nitrogen

T. Imanishi, T. Momose, I. Imanishi, 1978 .

Bicyclo[3.3.1]nonanes as synthetic intermediates. V. The Baeyer-Villiger oxidation of bicyclo[3.3.1]nonane-3,7-dione and its congeners.

T. Momose, S. Atarashi, 1979 .

Bicyclo [3. 3. 1]nonanes as Synthetic Intermediates. IV. Behavior of Bicyclo [3. n. 1] alkan-3-ones toward the Baeyer-Villiger Oxidation

O. Muraoka, T. Momose, S. Atarashi, 1979 .

Fluorinative Beckmann fragmentation: fluorinative alpha-cleavage of cyclic ketoximes by diethylaminosulfur trifluoride.

T. Momose, M. Kirihara, K. Niimi, 2000, Chemical & pharmaceutical bulletin.

Fluorinative α-cleavage of cyclic ketoximes withdiethylaminosulfur trifluoride: an efficient synthesis of fluorinatedcarbonitriles

T. Momose, M. Kirihara, K. Niimi, 1997 .

New synthesis of all the four isomers of 2-(2-hydroxypropyl)pyrrolidines via iterative asymmetric dihydroxylation to cause enantiomeric enhancement

H. Takahata, T. Momose, M. Kubota, 1997 .

Synthetic Studies on Lignans and Related Compounds. IV. Synthesis of Taiwanin C and E, and Justicidin D (Neojusticin A), E, and F (Taiwanin E Methyl Ether)

K. Kanai, T. Momose, Z. Horii, 1977 .

Synthetic Studies on Lignans and Related Compounds. III. Structure and Synthesis of Diphyllin

T. Momose, Z. Horii, Sangwon Kim, 1971 .

Synthetic Studies on Lignans and Related Compounds. II. Synthesis of 1-Hydroxy-3-hydroxymethyl-6,7-dimethoxy-4-(3,4-methylenedioxyphenyl)-2-naphthoic Acid γ-Lactone and Its Non-identity with Diphyllin

T. Momose, Z. Horii, Sangwon Kim, 1969 .

Synthetic Studies on Lignans and Related Compounds. I. Synthesis of 1-Hydroxy-3-hydroxymethyl-4-(3, 4-dimethoxyphenyl)-6, 7-methylenedioxy-2-naphthoic Acid γ-Lactone

T. Momose, Z. Horii, Sangwon Kim, 1968 .

Structure and synthesis of diphyllin

T. Momose, Z. Horii, S. Kim, 1968 .

Marine natural products. XXVI. Biologically active tridecapeptide lactones from the Okinawan marine sponge Theonella swinhoei (Theonellidae). (2). Structures of theonellapeptolides Ia, Ib, Ic, and Ie.

I. Kitagawa, M. Kobayashi, T. Momose, 1991, Chemical & pharmaceutical bulletin.

1, 6-Dihydro-3 (2H)-pyridinones. I. Facile Synthesis of N-Substituted 1, 6-Dihydro-3 (2H)-pyridinones

T. Imanishi, M. Hanaoka, T. Momose, 1982 .

Allylic Fluorides via the Cleavage of Tertiary Cyclopropyl Silyl Ethers with Diethylaminosulfur Trifluoride.

T. Momose, M. Kirihara, T. Kambayashi, 1996 .