H. Nemoto

发表

The enantioselective synthesis of poison-frog alkaloids (−)-203A, (−)-209B, (−)-231C, (−)-233D, and (−)-235B″

J. Daly, T. Spande, N. Toyooka, 2006 .

Alkaloids Indolizidine 235B′, Quinolizidine 1-epi-207I, and the Tricyclic 205B are Potent and Selective Noncompetitive Inhibitors of Nicotinic Acetylcholine Receptors

J. A. Dani, T. Sasaoka, N. Toyooka, 2004, Molecular Pharmacology.

Alkaloids Indolizidine 235 B , Quinolizidine 1-epi-207 I , and the Tricyclic 205 B are Potent and Selective Noncompetitive Inhibitors of Nicotinic Acetylcholine Receptors

J. A. Dani, T. Sasaoka, N. Toyooka, 2004 .

Efficient enantio- and diastereodivergent synthesis of poison-frog alkaloids 251O and trans-223B.

J. Daly, S. Kadota, Y. Tezuka, 2009, The Journal of organic chemistry.

Synthetic organic chemistry based on small ring compounds.

H. Nemoto, H. Nemoto*, 2007, Chemical & pharmaceutical bulletin.

Second generation of steroid synthesis via o-quinodimethane

H. Nemoto, K. Fukumoto, H. Nemoto*, 1998 .

A STEREOSELECTIVE SYNTHESIS OF 1 α-HYDROXY-VITAMIN D3

H. Nemoto, T. Kametani, K. Fukumoto, 1985 .

A facile ring-opening reaction of cyclobutenes: application to a synthesis of vitamin D3

H. Nemoto, T. Kametani, M. Tsubuki, 1983 .

Synthesis of Poison-Frog Alkaloids and Their Pharmacological Effects at Neuronal Nicotinic Acetylcholine Receptors

T. Sasaoka, N. Toyooka, H. Nemoto, 2007 .

Synthesis and biological evaluation of pyrethroid insecticide-derivatives as a chemical inducer for Bdnf mRNA expression in neurons.

M. Tsuda, M. Fukuchi, A. Tabuchi, 2012, Bioorganic & medicinal chemistry.

Construction of 4a,8a-cis-octahydroquinolin-7-one core using an intramolecular aldol type of cyclization: An application to enantioselective total synthesis of lepadin B

N. Toyooka, H. Nemoto, H. Takahata, 1999 .

Synthesis of new phorbol derivatives having ethereal side chain and evaluation of their anti-HIV activity.

M. Takeuchi, N. Yamamoto, H. Nemoto, 2005, Bioorganic & medicinal chemistry.

Synthesis of macrosphelides with a thiazole side chain: new antitumor candidates having apoptosis-inducing property.

Qing‐Li Zhao, T. Kondo, K. Ahmed, 2006, Organic letters.

A stereoselective synthesis of 1α-hydroxyvitamin D3

H. Nemoto, T. Kametani, K. Fukumoto, 1985 .

First enantioselective synthesis of (+)-quinolizidine 207I: determination of the absolute stereochemistry

N. Toyooka, H. Nemoto, 2003 .

A new method for selective epoxidation and a biogenetic-type synthesis of linalyloxides

H. Nemoto, T. Kametani, K. Fukumoto, 1978 .

Mechanism of apoptosis induced by a newly synthesized derivative of macrosphelides with a thiazole side chain.

T. Kondo, T. Sugiyama, Y. Yoshihisa, 2009, Chemico-biological interactions.

The role of a HSV thymidine kinase stimulating substance, scopadulciol, in improving the efficacy of cancer gene therapy

Y. Maitani, K. Hayashi, Jung-Bum Lee, 2006, The journal of gene medicine.

Vinyl cyclobutanol strategy for halogenated cyclopentanoids

H. Nemoto, K. Fukumoto, Motohiro Shiraki, 1995 .

A novel synthetic approach to the ecdysone side chain via furan derivatives

H. Nemoto, T. Kametani, M. Tsubuki, 1981 .

Synthesis of poison-frog alkaloids 237D, 207A, and two congeners of 235B' for evaluation to inhibitory effect of nicotinic acetylcholine receptors.

N. Toyooka, H. Nemoto, M. Kawasaki, 2005, Chemical & pharmaceutical bulletin.

Kinetically controlled ring-closing metathesis: synthesis of a potential scaffold for 12-membered salicylic macrolides.

H. Nemoto, Y. Matsuya, Sho Takayanagi, 2008, Chemistry.

Recent advances in the total synthesis of steroids via intramolecular cycloaddition reactions

H. Nemoto, T. Kametani, H. Nemoto*, 1981 .

Studies on the Syntheses of Heterocyclic Compounds. CDXVII. Syntheses of 1, 2-Benzoxazepine, Oxindole and Furanoquinolone Derivatives by Cyclization of Hydroxamic Acid with Polyphosphoric Acid

H. Nemoto, T. Kametani, 1971 .

Enzymic phenol oxidation of N-methylcoclaurine. Studies on the syntheses of heterocyclic compounds. Part cccxxxii†

H. Nemoto, T. Kametani, T. Kobari, 1970 .

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

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

Novel Access to Neopentyl-Type Halogenated Cyclopentanoids via Olefinic Cyclobutanols

H. Nemoto, K. Fukumoto, and Motohiro Shiraki, 1996 .

First enantioselective total synthesis of (+)-cortisone

H. Nemoto, M. Nagai, M. Imaizumi, 1990 .

A novel o-quinodimethane strategy for an active metabolite of vitamin D3. A total synthesis of 25-hydroxy windaus-grundmann ketone

H. Nemoto, K. Fukumoto, M. Ando, 1990 .

High diastereoselection in the intramolecular Diels–Alder reaction of o-quinodimethanes: an expedient entry to trans-benzoperhydrindans. A highly stereoselective total synthesis of (±)-estrone and (±)-adrenosterone

H. Nemoto, T. Kametani, M. Nagai, 1989 .

A novel approach to the stereocontrolled synthesis of steroid side chains including the CD-ring system: the first total synthesis of (+)-8.alpha.-(phenylsulfonyl)-des-AB-cholestane and its efficient conversion into Grundmann's ketone and vitamin D3

H. Nemoto, T. Kametani, K. Fukumoto, 1986 .

A GENERAL METHOD FOR THE STEREOSELECTIVE CONSTRUCTION OF DES-AB-CHOLESTANES. A FIRST TOTAL SYNTHESIS OF (+)-8α-PHENYLSULFONYL-DES-AB-CHOLESTANE

H. Nemoto, T. Kametani, K. Fukumoto, 1985 .

Evaluation of scopadulciol-related molecules for their stimulatory effect on the cytotoxicity of acyclovir and ganciclovir against Herpes simplex virus type 1 thymidine kinase gene-transfected HeLa cells.

K. Hayashi, Toshimitsu Hayashi, H. Ohno, 2004, Chemical & pharmaceutical bulletin.

An efficient synthesis of cholanic acids from 20-ketopregnanes

H. Nemoto, T. Kametani, K. Fukumoto, 1982 .

A New Protocol for the Consecutive α‐ and β‐Activation of Propiolates towards Electrophiles, Involving Conjugate Addition of Tertiary Amines and Intramolecular Silyl Migration

H. Nemoto, Y. Matsuya, Kousuke Hayashi, 2005 .

A novel modified baylis-hillman reaction of propiolate.

H. Nemoto, Y. Matsuya, Kousuke Hayashi, 2003, Journal of the American Chemical Society.

Synthesis of dihydrofuran-fused perhydrophenanthrenes having a phenolic hydroxyl group as a novel anti-Alzheimer's disease agent.

C. Tohda, N. Toyooka, H. Nemoto, 2012, Bioorganic & medicinal chemistry letters.

Synthesis of a new class of furan-fused tetracyclic compounds using o-quinodimethane chemistry and investigation of their antiviral Activity.

H. Ochiai, N. Toyooka, H. Nemoto, 2004, The Journal of organic chemistry.

A Novel Palladium-Mediated Cascade Reaction Triggered by Strain Release of the Cyclobutane System. A New General Route to Benzo- and Naphthohydrindans

Masahiro Yoshida, H. Nemoto, K. Fukumoto, 1997 .

A novel C(2)-symmetric 2,6-diallylpiperidine carboxylic acid methyl ester as a promising chiral building block for piperidine-related alkaloids.

H. Nemoto, H. Takahata, H. Ouchi, 2002, Organic letters.

Synthesis of poison-frog alkaloids 233A, 235U, and 251AA and their inhibitory effects on neuronal nicotinic acetylcholine receptors.

J. Daly, T. Sasaoka, T. Wada, 2007, Bioorganic & medicinal chemistry letters.

Flexible synthetic routes to poison-frog alkaloids of the 5,8-disubstituted indolizidine-class I: synthesis of common lactam chiral building blocks and application to the synthesis of (-)-203A, (-)-205A, and (-)-219F

J. Daly, T. Spande, N. Toyooka, 2007, Beilstein journal of organic chemistry.

Enantioselective syntheses of poison-frog alkaloids : 219F and 221I and an epimer of 193E

J. Daly, T. Spande, N. Toyooka, 2006 .

Stereodivergent synthesis of the 2,3,5,6-tetrasubstituted piperidine ring system: an application to the synthesis of alkaloids 223A and 205B from poison frogs

H. Shinoda, A. Fukutome, N. Toyooka, 2004 .

Asymmetric synthesis of 1-deoxynojirimycin and its congeners from a common chiral building block

H. Nemoto, A. Kato, I. Adachi, 2004 .

Aerobic oxidation of α-hydroxycarbonyls catalysed by trichlorooxyvanadium: efficient synthesis of α-dicarbonyl compounds

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

Enantioselective Synthesis of Poison-Frog Alkaloid 237D and Determination of Absolute Stereochemistry

J. Daly, T. Spande, N. Toyooka, 2005 .

Synthesis of alkaloid 223A and a structural revision.

J. Daly, T. Spande, A. Fukutome, 2002, Organic letters.

Synthesis of (-)-5-Epiindolizidine 167B and Formal Synthesis of 5E,9Z-Indolizidine 223AB

N. Toyooka, H. Nemoto, 2005 .

A concise and enantioselective approach to cyclobutanones by tandem asymmetric epoxidation and enantiospecific ring expansion of cyclopropylidene alcohols. An enantiocontrolled synthesis of (+)-and (-)-α-cuparenones

H. Nemoto, K. Fukumoto, M. Nagamochi, 1992 .

A new method for the synthesis of N-t-butoxycarbonyl protected α-alkoxy amines from allylamines under neutral conditions

Yoshinori Yamamoto, H. Jimenez, H. Nemoto, 1990 .

Palladium-catalyzed cascade ring expansion reaction of 1-(3-methoxycarbonyloxy-1-propynyl)cyclobutanols with phenols

M. Ihara, Masahiro Yoshida, H. Nemoto, 1999 .

Palladium-catalysed cascade ring expansion reaction of cyclobutanols that have a propargylic moiety with nucleophiles.

M. Ihara, Masahiro Yoshida, H. Nemoto, 2004, Organic & biomolecular chemistry.

A remarkable substituent effect on the enantioselectivity of tandem asymmetric epoxidation and enantiospecific ring expansion of cyclopropylidene alcohols: a new enantiocontrolled synthesis of (-)-debromoaplysin and (-)-aplysin

H. Nemoto, K. Fukumoto, M. Nagamochi, 1994 .

An asymmetric synthesis of benzylic quaternary carbon centers. A formal total synthesis of (−)-mesembrine

T. Tanabe, H. Nemoto, K. Fukumoto, 1994 .

Application of Chiral Building Blocks to the Synthesis of Drugs

N. Toyooka, H. Nemoto, 2003 .

Asymmetric synthesis of fagomine and its congeners

H. Nemoto, A. Kato, I. Adachi, 2001 .

Studies on the syntheses of heterocyclic compounds. Part DCXXII. Total synthesis of (±)-mappicine [7-(1-hydroxypropyl)-8-methyl-indolizino[1,2-b]quinolin-9(11H)-one]

H. Nemoto, T. Kametani, K. Fukumoto, 1975 .

Three-component coupling reaction and cyclization of N-tosylimines and TMS-substituted propiolate mediated by DABCO.

H. Nemoto, Y. Matsuya, Kousuke Hayashi, 2008, The Journal of organic chemistry.

Synthetic Studies on Biologically Active Alkaloids Starting from Lactam-type Chiral Building Blocks

N. Toyooka, H. Nemoto, 2004 .

Asymmetric synthesis of trans-benzoperhydroindan: asymmetric induction in intramolecular Diels–Alder reactions of o-quinodimethanes

H. Nemoto, T. Kametani, M. Nagai, 1988 .

New method for the synthesis of boron-10 containing nucleoside derivatives for neutron-capture therapy via palladium-catalyzed reaction

Yoshinori Yamamoto, H. Nemoto, T. Seko, 1989 .

Stereodivergent process for the synthesis of the decahydroquinoline type of dendrobatid alkaloids.

N. Toyooka, H. Nemoto, M. Okumura, 2002, The Journal of organic chemistry.

Asymmetric total synthesis of estradiol by an intramolecular cycloaddition of benzocyclobutene derivative

H. Matsumoto, H. Nemoto, T. Kametani, 1978 .

A formal regio- and stereoselective total synthesis of estrone. A convenient synthesis of D-homoestrone

H. Nemoto, T. Kametani, K. Fukumoto, 1976 .

Stereoselective approach to potential scaffold of A-nor B-aromatic OSW-1 analogues via [4+2] cycloaddition of o-quinodimethane

H. Nemoto, Kenji Sugimoto, Y. Matsuya, 2014 .

Enhancement of hyperthermia-induced apoptosis by a new synthesized class of benzocycloalkene compounds

Qing‐Li Zhao, T. Kondo, Da-yong Yu, 2008, Apoptosis.

Chiral cyclobutanones as versatile synthons: the first enantioselective total synthesis of (+)-laurene

H. Nemoto, K. Fukumoto, M. Nagamochi, 1993 .

Allenylcyclobutanol, a Versatile Initiator for the Palladium-Catalyzed Cascade Reaction: A Novel Route to Bicyclo[5.3.0] and -[6.3.0] Frameworks

H. Nemoto, K. Fukumoto, and Masahiro Yoshida, 1997 .

An Enantiocontrolled Formal Total Synthesis of (+)-Ipomeamarone, (-)-Ngaione, and Their Epimers

T. Tanabe, H. Nemoto, K. Fukumoto, 1993 .

A Novel Approach to Quaternary Substituted Chiral Cyclobutanes. A Formal Enantioselective Total Synthesis of 1,3-Dioxole Pheromone, (-)-Frontalin

T. Yamada, H. Nemoto, K. Fukumoto, 1991 .

Asymmetric construction of α,α–disubstituted cyclobutanones–enantioselective total synthesis of (–)-frontalin

T. Yamada, H. Nemoto, K. Fukumoto, 1991 .

Enantioselective syntheses of two 5, 9E diastereomers of 223V, an alkaloid from the poison frog Dendrobates pumilio

J. Daly, T. Spande, N. Toyooka, 2005 .

Asymmetric total synthesis of (+)-equilenin utilizing two types of cascade ring expansion reactions of small ring systems

M. Ihara, M. Ismail, Masahiro Yoshida, 2000 .

A Highly Enantiocontrolled Strategy for the Synthesis of Benzylic Quaternary Carbon Centers. A Formal Total Synthesis of (-)-Mesembrine

T. Tanabe, H. Nemoto, K. Fukumoto, 1995 .

The first example of asymmetric dihydroxylation of cyclopropylidene derivatives—An enantioenriched formal total synthesis of (−)-filiformin

H. Hakamata, H. Nemoto, K. Fukumoto, 1995 .

A novel access to hydrindan derivatives by palladium mediated tandem ring expansion and insertion reaction of alkenic cyclobutanols

H. Nemoto, K. Fukumoto, Motohiro Shiraki, 1994 .

Synthetic studies toward to 1α-hydroxyvitamin D3 — stereoselective synthesis of (±)-(Z)-2-(3β, 5α-dihydroxy-2-methylenecyclohexylidene) ethylidenecyclohexane

M. Ihara, Xiaomei Wu, H. Nemoto, 1983 .

New strategy for the total synthesis of macrosphelides a and B based on ring-closing metathesis.

H. Nemoto, Y. Matsuya, T. Kawaguchi, 2003, Organic letters.

Ring expansion of cyclopropylmethanols to cyclobutanes—an enantioselective total synthesis of (R)-(+)-dodecan-5-olide, and (S)-(+)- and (R)-(–)-5-[(Z)-dec-1-enyl]dihydrofuran-2(3H)-one

H. Nemoto, K. Fukumoto, M. Mori, 1990 .

Structure-activity-relationship studies on dihydrofuran-fused perhydrophenanthrenes as an anti-Alzheimer's disease agent.

C. Tohda, N. Toyooka, H. Nemoto, 2013, Bioorganic & medicinal chemistry.

Concise and highly stereocontrolled synthesis of 1-deoxygalactonojirimycin and its congeners using dioxanylpiperidene, a promising chiral building block.

H. Nemoto, H. Takahata, H. Ouchi, 2003, Organic letters.

A practical route for enantioselective total synthesis of (+)-11-deoxy-19-norcorticosterone via intramolecular Diels–Alder addition to an ortho-quinodimethane

A. Satoh, H. Nemoto, K. Fukumoto, 1991 .

A facile and enantioselective total synthesis of (+)-19-nordeoxycorticosterone

A. Satoh, H. Nemoto, K. Fukumoto, 1990 .

Syntheses of aza-analogues of macrosphelides via RCM strategy and their biological evaluation

T. Kondo, N. Toyooka, H. Nemoto, 2011 .

Concerted ring-opening reaction of cyclobutenes. The extraordinary accelerating effects of arylsulfoxy and sulfonyl carbanion substituents

H. Nemoto, T. Kametani, M. Tsubuki, 1981 .

Asymmetric synthesis of the four possible fagomine isomers.

H. Nemoto, A. Kato, I. Adachi, 2003, The Journal of organic chemistry.

Efficient approach to 1,2-diazepines via formal diazomethylene insertion into the C-C bond of cyclobutenones.

Kenji Sugimoto, N. Toyooka, H. Nemoto, 2012, Organic letters.

A new stereocontrolled access to angularly disubstituted cis-decalinsvia tandem radical ring expansion and cyclization

H. Nemoto, K. Fukumoto, Motohiro Shiraki, 1996 .

An aromatic version of claisen rearrangements of ester silyl enolates: a facile synthesis of 2,3-disubstituted furans

H. Nemoto, T. Kametani, K. Fukumoto, 1985 .

A simple and stereoselective synthesis of Des-A-B-aromatic corticoids via intramolecular cycloaddition: potential intermediates for the synthesis of corticoids

H. Nemoto, T. Kametani, M. Nagai, 1985 .

Studies on the syntheses of heterocyclic and natural compounds. 950. Asymmetric total synthesis of (+)-chenodeoxycholic acid. Stereoselectivity of intramolecular cycloaddition of olefinic o-quinodimethanes

H. Nemoto, T. Kametani, Koji Suzuki, 1982 .

Total Synthesis of (±)-Scirpene

M. Ihara, H. Nemoto, and Eiki Takahashi, 1999 .

The first enantioselective total synthesis of (+)-laurene

H. Nemoto, K. Fukumoto, M. Nagamochi, 1992 .

A simple and efficient total synthesis of the sesquiterpenes cuparene and iso-α-curcumene, from furan derivatives

H. Nemoto, T. Kametani, M. Tsubuki, 1980 .

Annelation Reaction by Using Heterocyclic Compounds

H. Nemoto, T. Kametani, H. Nemoto*, 1978 .

An improved and practical method for the synthesis of optically active diethyl tartrate dibenzyl ether

S. Takamatsu, Yoshinori Yamamoto, H. Nemoto, 1991 .

First total synthesis of (+)-chenodeoxycholic acid

H. Nemoto, T. Kametani, Koji Suzuki, 1981 .

A novel strategy for the enantioselective synthesis of the steroidal framework using cascade ring expansion reactions of small ring systems-asymmetric total synthesis of (+)-equilenin

M. Ihara, Masahiro Yoshida, H. Nemoto, 1999 .

Diels-Alder Reactions with o-Quinodimethanes: The influence of protective groups and substituents of allyl alcohols on the stereochemical course—A new access to 18-trifluoroestrans

A. Satoh, H. Nemoto, K. Fukumoto, 1995 .

Studies on the stereochemical course of intramolecular cycloaddition reactions of olefinic o-quinodimethanes-stereoselective synthesis of 8α, 9α, 14β-estranes

M. Aizawa, H. Nemoto, T. Kametani, 1981 .

A stereocontrolled total synthesis of 2β,3β,20β-triacetoxy-5α-pregnan-6-one — A total synthesis of 20-hydroxyecdysone

H. Nemoto, T. Kametani, M. Tsubuki, 1980 .

Hydroxylation of benzylic and allylic sites by plant cultured suspension cells

H. Hamada, T. Furuya, H. Nemoto, 2001 .

Total synthesis of (±)-4-deoxyverrucarol; a new route to trichothecanes via ring expansion of small ring compounds

M. Ihara, H. Nemoto, J. Miyata, 1999 .

Studies on the synthesis of heterocyclic compounds. Part 832. A simple and efficient synthesis of apomitomycin derivatives; a potential intermediate for mitomycin synthesis

M. Ihara, H. Nemoto, T. Kametani, 1980 .

TRANSITION METAL CATALYZED ADDITION OF CERTAIN NUCLEOPHILES TO IMINES

N. Asao, H. Nemoto, Y. Yamamoto, 1994 .

Recent Advances in Macrosphelide Synthesis

H. Nemoto, Y. Matsuya, H. Nemoto*, 2005 .

Synthetic Studies on Poison-Frog Alkaloid 261C

S. Kadota, Y. Tezuka, S. Awale, 2005 .

Aerobic deprotection of monothioacetals catalyzed by trichlorooxyvanadium

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

A highly stereoselective total synthesis of (±)-estrone and (±)-adrenosterone

H. Nemoto, T. Kametani, M. Nagai, 1988 .

Asymmetric synthesis of (-) -3.beta.-hydroxy-17-methoxy-D-homo-18-nor-5.alpha.-androsta-13,15,17-triene

H. Nemoto, T. Kametani, Koji Suzuki, 1980 .

Total synthesis of (+)-5α-dihydropregnenolone via acetylene-cation cyclization

H. Nemoto, T. Kametani, Koji Suzuki, 1980 .

Design, synthesis, and biological evaluation of artificial macrosphelides in the search for new apoptosis-inducing agents.

Qing‐Li Zhao, T. Kondo, Da-yong Yu, 2009, Chemistry.

A New Selenium-Assisted Cyclization-A Biogenetic-type Synthesis of Safranal

H. Nemoto, T. Kametani, H. Kurobe, 1981 .

A NEW SELENIUM-ASSISTED CYCLIZATION - A BIOGENETIC-TYPE SYNTHESIS OF SAFRANAL

H. Nemoto, T. Kametani, H. Kurobe, 1981 .

Stereoselective olefinic cyclization assisted by the selenyl group — biogenetic-type synthesis of caparrapi oxide

H. Nemoto, T. Kametani, K. Fukumoto, 1981 .

Stereoselective olefin cyclization mediated by the selenyl group; direct formation of a selenyl caparrapi oxide

H. Nemoto, T. Kametani, K. Fukumoto, 1982 .

Stereoselective cyclization assisted by the selenyl group. Biogenetic-type synthesis in the p-menthane series

H. Nemoto, T. Kametani, H. Kurobe, 1981 .

New method for carbon–carbon bond formation: biogenetic-type synthesis of safranal

H. Nemoto, T. Kametani, H. Kurobe, 1979 .

Marine alkaloids (-)-pictamine and (-)-lepadin B block neuronal nicotinic acetylcholine receptors.

J. A. Dani, T. Sasaoka, N. Toyooka, 2005, Biological & pharmaceutical bulletin.

Asymmetric synthesis of the four possible fagomine isomers.

H. Nemoto, A. Kato, I. Adachi, 2003, Journal of Organic Chemistry.

ARTIFICIAL MACROSPHELIDES AS A NOVEL APOPTOSIS-INDUCING COMPOUND

H. Nemoto, Y. Matsuya, 2010 .

TOTAL SYNTHESIS OF 2-NOR-MACROSPHELIDES A AND B

H. Nemoto, Y. Matsuya, Takashi Matsushita, 2009 .

Rapid and transient intracellular oxidative stress due to novel macrosphelides trigger apoptosis via Fas/caspase-8-dependent pathway in human lymphoma U937 cells.

Qing‐Li Zhao, T. Kondo, Da-yong Yu, 2007, Chemico-biological interactions.

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 .

A practical asymmetric synthesis of trans-4,5-benzhydrindan-1-ones as a precursor of A-nor B-aromatic steroidal compounds.

H. Nemoto, Y. Matsuya, Seiji Masuda, 2005, The Journal of organic chemistry.

Total Synthesis of A‐Nor B‐Aromatic OSW‐1 Aglycon: A Highly Effective Approach to Optically Active trans‐4,5‐Benzhydrindane

H. Nemoto, Y. Matsuya, T. Itoh, 2003 .

A novel chiral approach to trans-3a,4,5,9b-tetrahydro-1H-benz[e]indene

A. Satoh, H. Nemoto, K. Fukumoto, 1992 .

A novel strategy for the stereoselective total synthesis of C-17 spiro steroids. Total synthesis of 19-norcanrenone - a formal total synthesis of 19-norspironolactone

H. Nemoto, T. Kametani, M. Nagai, 1988 .

A Novel Chiral Approach to trans‐3a,4,5,9b‐Tetrahydro‐1H‐benz(e)indene.

A. Satoh, H. Nemoto, K. Fukumoto, 1992 .

A novel approach to optically active trans-benzoperhydroindan (2,3,3a,3b,4,5-hexahydro-1 H-benz[e]indene)

H. Nemoto, K. Fukumoto, N. Matsuhashi, 1991 .

A novel stereoselective access to des-A B-aromatic corticosteroids via intramolecular cycloaddition reaction—potential intermediates for the synthesis of corticosteroids

H. Nemoto, T. Kametani, M. Nagai, 1987 .

A stereoselective total synthesis of 11-oxoprogesterone, a precursor to the corticosteroids, via an intramolecular cycloaddition reaction

H. Nemoto, T. Kametani, M. Nagai, 1986 .

Concise and practical approach to chiral des-A B-trienic corticosteroids

A. Satoh, H. Nemoto, K. Fukumoto, 1994 .

Rapid enantioselective access to des-AB-trienic corticosteroids via intramolecular cycloaddition

A. Satoh, H. Nemoto, K. Fukumoto, 1993 .

Synthesis and antitumor activity of des-AB analogue of steroidal saponin OSW-1

H. Sakurai, N. Toyooka, H. Nemoto, 2013 .

Studies toward intramolecular cycloaddition of o-quinodimethane with an oxazole moiety

H. Nemoto, Y. Matsuya, Hong-Bo Qin, 2009 .

Synthesis and antitumor activity of the estrane analogue of OSW-1

H. Nemoto, Y. Matsuya, T. Tschamber, 2005 .

Total Synthesis of A-Nor B-Aromatic OSW-1 Aglycon: A Highly Effective Approach to Optically Active trans-4,5-Benzhydrindan.

H. Nemoto, Y. Matsuya, T. Itoh, 2003 .

A Novel Strategy for the Stereoselective Total Synthesis of C-17 Spiro Steroids. Total Synthesis of 19-Norcanrenone, a Formal Total Synthesis of 19-Norspironolactone.

H. Nemoto, T. Kametani, M. Nagai, 1988 .

A Stereoselective Total Synthesis of 11-Oxoprogesterone, a Precursor to the Corticosteroids, via an Intramolecular Cycloaddition Reaction.

H. Nemoto, T. Kametani, M. Nagai, 1987 .

Model studies toward the total synthesis of halenaquinol and halenaquinone

N. Toyooka, H. Nemoto, H. Kakuda, 2002 .

A new stereocontrolled synthesis of d-ring aromatic steroid

H. Nemoto, T. Kametani, H. Nemoto*, 1979 .

The asymmetric total synthesis of estradiol by an intramolecular cycloaddition reaction of o-quinodimethane

H. Matsumoto, H. Nemoto, T. Kametani, 1978 .

Concise and Practical Approach to Chiral Des‐A B‐Trienic Corticosteroids.

A. Satoh, H. Nemoto, K. Fukumoto, 1994 .

Rapid Enantioselective Access to Des-AB-trienic Corticosteroids via Intramolecular Cycloaddition.

A. Satoh, H. Nemoto, K. Fukumoto, 1994 .

Studies Toward Intramolecular Cycloaddition of o‐Quinodimethane with an Oxazole Moiety.

H. Nemoto, Y. Matsuya, Hong-Bo Qin, 2009 .

Approach to a New Dihydrofuran-Fused Cyclic System by a Remarkable Switching of endo/exo Selectivity of a [4+2] Cycloaddition Reaction

H. Ochiai, H. Nemoto, T. Miyahara, 2008 .

Enhancement of hyperthermia-induced apoptosis by a new synthesized class of furan-fused tetracyclic compounds

Qing‐Li Zhao, T. Kondo, Da-yong Yu, 2007, Apoptosis.

Synthesis and biological evaluation of dihydrofuran-fused perhydrophenanthrenes as a new anti-influenza agent having novel structural characteristic.

H. Ochiai, H. Nemoto, Y. Matsuya, 2007, Bioorganic & medicinal chemistry.

Facile transformation of benzocyclobutenones into 2,3-benzodiazepines via 4pi-8pi tandem electrocyclic reactions involving net insertion of diazomethylene compounds.

H. Nemoto, Y. Matsuya, N. Ohsawa, 2006, Journal of the American Chemical Society.

Accelerated electrocyclic ring-opening of benzocyclobutenes under the influence of a beta-silicon atom.

H. Nemoto, Y. Matsuya, N. Ohsawa, 2006, Journal of the American Chemical Society.

Synthesis of New Potentially Antiviral Furan-fused Compounds by Thermolysis of Benzocyclobutene Derivatives

H. Nemoto, Y. Matsuya, Hong-Bo Qin, 2004 .

Rapid Access to the Potential Intermediate for the Synthesis of Halenaquinol and Halenaquinone

N. Toyooka, H. Nemoto, H. Kakuda, 2001 .

Competitive reactions between sigmatropic reaction and cycloaddition affected by geometry of o-quinodimethanes

M. Ihara, H. Nemoto, T. Kametani, 1977 .

OSW-1 analogues: modification of the carbohydrate moiety.

H. Nemoto, Y. Matsuya, T. Tschamber, 2007, Bioorganic & medicinal chemistry letters.

Synthesis of the N-Terminus of Glycopeptide Unit for Aeruginosin 205-A

N. Toyooka, H. Nemoto, A. Nakazawa, 2003 .

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 .

Boron-10 carriers for NCT: a new synthetic method via condensation with aldehydes having boronic moiety

Yoshinori Yamamoto, H. Nemoto, F. Rong, 1989 .

Novel stereoselective total synthesis of 14α-hydroxyestrone methyl ether

H. Nemoto, T. Kametani, M. Tsubuki, 1979 .

DIHYDROAZAMACROSPHELIDES : SYNTHESIS AND APOPTOSIS INDUCING ACTIVITIES

T. Kondo, N. Toyooka, H. Nemoto, 2011 .

A New Water-soluble p-Boronophenylalanine Derivative for Neutron Capture Therapy

S. Iwamoto, Yoshinori Yamamoto, H. Nemoto, 1993 .

Studies on the syntheses of heterocyclic compounds. Part CDLXII. Total photolytic syntheses of aporphine [(±)-N-methyl-laurotetanine, (±)-cassythicine, and (±)-pukateine], proaporphine [(±)-orientalinone], and morphinandienone [(±)-pallidine and (±)-salutaridine] alkaloids

S. Shibuya, H. Nemoto, K. Fukumoto, 1972 .

A novel and efficient route to chiral A-ring aromatic trichothecanes—The first enantiocontrolled total synthesis of (-)-debromofiliformin and (-)-filiformin

H. Hakamata, H. Nemoto, K. Fukumoto, 1995 .

Novel Phorbol Esters Exert Dichotomous Effects on Inhibition of HIV-1 Infection and Activation of Latent HIV-1 Expression

N. Yamamoto, H. Nemoto, Yu Zhong, 2005, Antiviral chemistry & chemotherapy.

Total synthesis of macrosphelides A, B, and E: first application of ring-closing metathesis for macrosphelide synthesis.

H. Nemoto, Y. Matsuya, T. Kawaguchi, 2004, The Journal of organic chemistry.

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.

Novel 3,4-diazabenzotropone compounds (2,3-benzodiazepin-5-ones): synthesis, unique reactivity, and biological evaluation.

T. Kondo, H. Nemoto, Zheng-li Wei, 2009, Organic Letters.

Total synthesis of the antipode of alkaloid 205 B.

H. Shinoda, A. Fukutome, N. Toyooka, 2003, Angewandte Chemie.

A novel and general route to diverse A-ring aromatic trichothecanes via cyclobutanes

H. Nemoto, K. Fukumoto, J. Miyata, 1996 .

Flexible synthesis of poison-frog alkaloids of the 5,8-disubstituted indolizidine-class. II: Synthesis of (-)-209B, (-)-231C, (-)-233D, (-)-235B", (-)-221I, and an epimer of 193E and pharmacological effects at neuronal nicotinic acetylcholine receptors.

J. Daly, T. Sasaoka, T. Wada, 2007 .

Cyclic carbonates, novel expandable monomers on polymerization

T. Endo, T. Takata, F. Sanda, 1997 .

Treatment with SRT1720, a SIRT1 activator, ameliorates fatty liver with reduced expression of lipogenic enzymes in MSG mice.

K. Tsuneyama, K. Tobe, I. Usui, 2009, American journal of physiology. Endocrinology and metabolism.

Synthesis of Macrosphelides Containing a Heterocyclic Side Chain as a Novel Apoptosis Inducer

Da-yong Yu, Tomomi Kawamura, T. Kondo, 2010 .

Synthesis of Macrosphelides Containing a Heterocyclic Side Chain as a Novel Apoptosis Inducer.

Da-yong Yu, Tomomi Kawamura, T. Kondo, 2010 .

Studies on the Syntheses of Heterocyclic Compounds. DCLXXII. A Synthesis of Coralydine and O-Methylcorytenchirine by Thermolysis of Benzocyclobutene

H. Nemoto, T. Kametani, K. Fukumoto, 1976 .

Total synthesis of steroid hormones. Efficient stereocontrolled synthesis of 17-methoxy-6-oxo-D-homo-18-nor-5.beta.-androsta-2,13,15,17-tetraene

H. Nemoto, T. Kametani, M. Tsubuki, 1980 .

Synthesis of sominone and its derivatives based on an RCM strategy: discovery of a novel anti-Alzheimer's disease medicine candidate "denosomin".

Y. Yamakawa, C. Tohda, M. Yamada, 2009, Organic letters.