M. Hanaoka

发表

Rh(I)-catalyzed intramolecular allenic Pauson-Khand reaction: construction of a bicyclo[5.3.0]dec-1,7-dien-9-one skeleton.

C. Mukai, Izumi Nomura, K. Yamanishi, 2002, Organic letters.

A highly stereoselective synthesis of (±)-dihydrofumariline-1

C. Mukai, M. Hanaoka, M. Iwasaki, 1985 .

Photochemical valence tautomerization of berberinephenolbetaines to 8,14-cycloberbines, versatile aziridine derivatives for spirobenzylisoquinolines

T. Imanishi, M. Hanaoka, S. Yasuda, 1979 .

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 .

Stereoselective Total Synthesis of (+/-)-Swainsonine Based on Endo Mode Cyclization.

C. Mukai, M. Hanaoka, Yu-ichi Sugimoto Yi, 1998, The Journal of organic chemistry.

An optically active chromium(0)-complexed benzaldehyde in organic synthesis: A highly stereocontrolled asymmetric synthesis of (2R,3S)-(-)-N-benzoyl-3-phenylisoserine methyl ester, the taxol C-13 side chain analogue

C. Mukai, M. Hanaoka, I. Kim, 1992 .

1,6-DIHYDRO-3 (2H)-PYRIDINONES AS SYNTHETIC INTERMEDIATES. TOTAL SYNTHESIS OF (±)-EBURNAMONINE

T. Imanishi, M. Inoue, M. Hanaoka, 1982 .

Stereocomplementary Construction of Optically Active Bicyclo[4.3.0]nonenone Derivatives.

Jin Sung Kim, C. Mukai, M. Hanaoka, 1999, The Journal of organic chemistry.

Structure of securinine.

M. Hanaoka, Y. Tamura, Z. Horii, 1963, Tetrahedron.

Formal synthesis of nitidine through palladium-catalyzed isocoumarin synthesis

M. Hanaoka, T. Minami, A. Nishimoto, 1995 .

A New Total Synthesis of Oxyterihanine

C. Mukai, M. Hanaoka, N. Kobayashi, 1987 .

Transformation of protoberberines into benzo[C]phenanthridines a novel and efficient synthesis of antitumor benzo[C]phenanthridine alkaloids, fagaronine and nitidine

M. Marutani, C. Mukai, H. Yamagishi, 1984 .

New glycosylation reaction based on alkyne-Co2(CO)6 complex

C. Mukai, M. Hanaoka, T. Itoh, 1997 .

SYNTHESIS OF 3-SUBSTITUTED ISOCOUMARINS THROUGH ACYLOXYPALLADATION OF o-ALKENYLBENZOIC ACIDS

Yumio Nakamura, M. Hanaoka, T. Minami, 1994 .

INVERSION OF A HYDROXYL GROUP BY THE NEIGHBORING-GROUP PARTICIPATION OF A URETHANE : A GENERAL AND STEREOSELECTIVE SYNTHESIS OF (±)-RADDEANONE, (±)-YENHUSOMIDINE, AND RELATED SPIROBENZYLISOQUINOLINE ALKALOIDS

M. Hanaoka, S. Yasuda, Masumi Kohzu, 1988 .

A convenient transformation of spirobenzylisoquinolines to dehydrophthalideisoquinolines.

S. Kim, M. Hanaoka, S. Yasuda, 1988 .

A NOVEL AND HIGHLY STEREOSELECTIVE SYNTHESIS OF (±)-SIBIRICINE

M. Hanaoka, S. Yasuda, Masumi Kohzu, 1985 .

Chemical Transformation of Protoberberines. XIII. A Novel and Efficient Synthesis of Antitumor Benzo [c] phenanthridine Alkaloids, Nitidine and Fagaronine

M. Marutani, C. Mukai, H. Yamagishi, 1987 .

Studies on total syntheses of antitumor styryllactones: Stereoselective total syntheses of (+)-goniofufurone, (+)-goniobutenolide A, and (−)-goniobutenolide B

C. Mukai, M. Hanaoka, M. Kido, 1996 .

A new entry to oxacycles via base-catalyzed endo mode cyclization of allenyl sulfoxides and sulfones.

H. Yamashita, C. Mukai, M. Hanaoka, 2001, Organic letters.

Diastereocomplementary construction of optically active bicyclo[4.3.0]nonenone skeleton based on Pauson-Khand reaction

Jin Sung Kim, C. Mukai, M. Uchiyama, 1998 .

Stereoselective construction of optically active bicyclo[3.3.0]octenone derivatives based on the Pauson–Khand reaction

Jin Sung Kim, C. Mukai, M. Uchiyama, 1998 .

A highly diastereoselective construction of optically active bicyclo[3.3.0]octenone derivatives from L-ascorbic acid via Pauson-Khand reaction

C. Mukai, M. Uchiyama, M. Hanaoka, 1995 .

Bis(cyclopentadienyl)tetracarbonyldimolybdenum-alkyne complexes mediated [2 + 2 + 1] cycloaddition: the formation of 3-substituted cyclopentenone derivatives

C. Mukai, M. Uchiyama, M. Hanaoka, 1992 .

Dicobalt hexacarbonyl-complex of propynals in organic synthesis: Erythro-selective aldol reaction of cobalt-complexed propynals with silyl enol ethers

C. Mukai, M. Hanaoka, K. Nagami, 1989 .

A novel total synthesis of (±)-cryptaustoline, a dibenzopyrrocoline alkaloid

M. Hanaoka, S. Yasuda, S. Yoshida, 1989 .

First Total Synthesis of (+)-Secosyrin 1

C. Mukai, M. Hanaoka, Sameh M. Moharram, 1997 .

NEW APPROACH TO AI-77B: STEREOSELECTIVE CONSTRUCTION OF A POTENTIAL PRECURSOR OF THE AMINO ACID SIDE CHAIN

C. Mukai, M. Hanaoka, Motonori Miyakawa, 1997 .

syn-Selective aldol reaction of propynal–hexacarbonylcobalt complexes with ketene silyl acetals

C. Mukai, M. Hanaoka, K. Nagami, 1992 .

A Highly Stereoselective Synthesis of the N-Terminal Amino Acid Analogue of Nikkomycin B and Bx

C. Mukai, M. Hanaoka, Motonori Miyakawa, 1994 .

Regioselective and stereospecific formation of 2-ethynyl-3-hydroxytetrahydropyran derivatives via 6-endo ring closure

C. Mukai, M. Hanaoka, Y. Sugimoto, 1994 .

Chemical Transformation of Protoberberines. III. Convenient Synthesis of 8-Methoxyberberinephenolbetaine by Photooxygenation of Berberine. A Novel Conversion of Berberine into (±)-Ophiocarpine, (±)-Epiophiocarpine, (±)-α-Hydrastine, and (±)-β-Hydrastine

C. Mukai, M. Hanaoka, Y. Arata, 1983 .

Transformation of (±)-Ophiocarpine and (±)-13-Epiophiocarpine to (±)-α- and (±)-β-Hydrastine with Complete Retention of Configuration

T. Imanishi, M. Hanaoka, K. Nagami, 1979 .

Photo-oxygenation of Berberine. A Novel Conversion of Berberine to (±)-Ophiocarpine, (±)-a- and (±)-b-Hydrastine

C. Mukai, M. Hanaoka, Y. Arata, 1977 .

Chapter 3 Transformation Reactions of Protoberberine Alkaloids

M. Hanaoka, 1988 .

An alternative procedure for the stereoselective formation of tetrahydropyran derivatives via 6-endo ring closure

C. Mukai, M. Hanaoka, Y. Sugimoto, 1994 .

Optically active tricarbonyl(η6-o-trimethylsilylbenzaldehyde)chromium(O) complexes in organic synthesis: a highly diastereoselective 1,3-dipolar cycloaddition with electron-rich olefins

W. Cho, C. Mukai, M. Hanaoka, 1993 .

Optically active tricarbonyl[.eta.6-o-(trimethylsilyl)benzaldehyde]chromium(0) complexes in organic synthesis: a highly anti-selective asymmetric aldol reaction with O-silyl ketene O,S-acetals

C. Mukai, M. Hanaoka, A. Mihira, 1992 .

Asymmetric aldol reaction : a highly Erythro-selective aldol reaction between tricarbonyl(O-trimethylsilylbenzaldehyde derivative)- chromium(0) complexes and cyclic silyl enol ethers

W. Cho, C. Mukai, M. Hanaoka, 1991 .

Tricarbonyl(benzaldehyde)chromium(0) complexes in organic synthesis: A highly stereoselective 1,3-dipolar cycloaddition of chromium(0)-complexed nitrones

C. Mukai, M. Hanaoka, Jea Cho Won, 1990 .

A highly erythro selective aldol reaction between chromium-complexed benzaldehyde derivatives and cyclic silyl enol ethers

W. Cho, C. Mukai, M. Hanaoka, 1989 .

An optically active chromium(0)-complexed benzaldehyde derivative in organic synthesis: A highly stereocontrolled total synthesis of (+)-goniofufurone

C. Mukai, M. Hanaoka, I. Kim, 1993 .

Tricarbonyl(η6-o-(trimethylsilyl)benzaldehyde)chromium(0) Complexes in Organic Synthesis: A Highly Anti-Selective Asymmetric Aldol Reaction with O-Silyl Ketene O,S-Acetals.

C. Mukai, M. Hanaoka, A. Mihira, 1992 .

Erythro-Selective Aldol Reaction of Tricarbonyl(η 6 -o-trialkylsilylbenzaldehyde)chromium(0) Complexes with Cyclic Ketene Silyl Acetals

C. Mukai, M. Hanaoka, A. Mihira, 1991 .

Asymmetric Aldol Reaction: A Highly erythro‐Selective Aldol Reaction Between Tricarbonyl(o‐trimethylsilylbenzaldehyde derivative)chromium(0) Complexes and Cyclic Silyl Enol Ethers.

W. Cho, C. Mukai, M. Hanaoka, 1991 .

First total synthesis of (-)-ichthyothereol and its acetate.

C. Mukai, N. Miyakoshi, M. Hanaoka, 2001, The Journal of organic chemistry.

A New Procedure for Construction of Oxocane and Oxonane Derivatives Based on Alkyne–Co2(CO)6 Complexes

C. Mukai, M. Hanaoka, H. Yamashita, 2000 .

Highly stereocontrolled asymmetric syntheses of taxol and taxotère C-13 side chain analogues

C. Mukai, M. Hanaoka, I. Kim, 1993 .

1, 6-Dihydro-3 (2H)-pyridinones. VII. Stereoselective Total Synthesis of a Monoterpene Alkaloid, (±)-Tecomanine

T. Imanishi, M. Hanaoka, N. Yagi, 1983 .

1,6-dihydro-3(2H)-pyridinones as synthetic intermediates. Total synthesis of (±)-tecomanine

T. Imanishi, M. Hanaoka, N. Yagi, 1981 .

A new procedure for highly stereoselective and regioselective synthesis of 2-ethynyl-3-hydroxytetrahydropyran derivatives based on alkyne-Co2(CO)6 complex

C. Mukai, M. Hanaoka, Y. Sugimoto, 1998 .

Total synthesis of (′)-ceratopicanol

Minoru Kobayashi, C. Mukai, M. Hanaoka, 2002 .

Trimethylsilyl Trifluoromethanesulfonate-Catalyzed Aldol Reaction of Various Aldehydes with Silyl Enol Ethers

C. Mukai, M. Hanaoka, K. Nagami, 1990 .

A novel and biomimetic synthesis of (.+-.)-chelamine, (.+-.)-chelidonine, sanguinarine, and dihydrosanguinarine from coptisine via a common intermediate.

C. Mukai, M. Hanaoka, S. Yoshida, 1986 .

A stereoselective synthesis of (±)-homochelidonine

C. Mukai, M. Hanaoka, S. Yoshida, 1985 .

Highly diastereoselective aldol reactions of cobalt-complexed and uncomplexed propynals with O-silyl ketene O,S-ketals : highly stereoselective divergent formal syntheses of the β-lactam antibiotics (±)-PS-5 and (±)-epi-PS-5

C. Mukai, M. Hanaoka, O. Kataoka, 1993 .

A highly diastereoselective aldol reaction of dicobalt hexacarbonyl propynal complex and uncomplexed propynal: A stereoselective divergent synthesis of (±)-PS-5 and (±)-6-Epi-PS-5

C. Mukai, M. Hanaoka, O. Kataoka, 1991 .

1,6-Dihydro-3(2H)-pyridinones as synthetic intermediates. A convenient total synthesis of (.+-.)-cleavamine.

T. Imanishi, M. Hanaoka, A. Nakai, 1981 .

Dicobaltoctacarbonyl-Mediated Deoximation.

C. Mukai, Izumi Nomura, M. Hanaoka, 2000 .

Synthesis of α,β-unsaturated aldehydes through palladium catalyzed regioselective hydrogen migration

M. Hanaoka, T. Minami, 1994 .

Stereocomplementary construction of 2-ethynyl-3-hydroxytetrahydrofuran derivatives via endo-mode ring closure of 3,4-epoxy-6-substitutedhex-5-yn-1-ols

C. Mukai, M. Hanaoka, Y. Sugimoto, 1994 .

The total synthesis of securinine and virosecurinine

M. Hanaoka, Y. Tamura, H. Nakai, 1967 .

New Glycosylation Reaction Based on Alkyne-Co2(CO)6 Complex.

C. Mukai, M. Hanaoka, T. Itoh, 1997 .

Studies on synthesis of optically active twelve-membered diynes: a convergent construction of a twelve-membered diketodiyne compound with C2 symmetry

C. Mukai, M. Hanaoka, E. Kasamatsu, 2000 .

Formal Synthesis of Nitidine Through Palladium‐Catalyzed Isocoumarin Synthesis.

M. Hanaoka, T. Minami, A. Nishimoto, 1996 .

DICOBALTOCTACARBONYL-MEDIATED DEOXIMATION

C. Mukai, Izumi Nomura, M. Hanaoka, 1999 .

A NOVEL SYNTHESIS OF QUINAZOLINEQUINONE AND CARBAZOLEQUINONE THROUGH ANIONIC CYCLOADDITION : ITS APPLICATION TO A SYNTHESIS OF MURRAYAQUINONE A

M. Hanaoka, A. Wada, Syuichi Hirai, 1994 .

A cobalt-complexed propyanl in organic synthesis: A highly stereoselective total synthesis of bengamide E

C. Mukai, M. Hanaoka, O. Kataoka, 1994 .

An efficient method for the optical resolution of 3-hydroxy-2-substituted-4-alkynoates: a highly stereoselective total synthesis of (+)-bengamide E1

C. Mukai, M. Hanaoka, O. Kataoka, 1995 .

Studies on antispasmodics. V. Synthesis and anticholinergic activity of N-alkyl 1- and 2-diarylmethylene-indolizidinium bromides.

H. Kato, M. Hanaoka, S. Kubo, 1980, Chemical & pharmaceutical bulletin.

Synthetic Studies on Securitinine and Related Compounds. I. Stereochemistries of the Catalytic Hydrogenation Products of 6-(4-Methoxy-2-pyridyl)-1, 4-dioxaspiro [4, 5] decan-6-ol

T. Imanishi, M. Hanaoka, Tetsuaki Tanaka, 1972 .

Structure of phyllantidine

T. Imanishi, M. Hanaoka, M. Yamauchi, 1972 .

Potential cancer chemopreventive activity of simple isoquinolines, 1-benzylisoquinolines, and protoberberines.

Kazuyoshi Takeda, Harukuni Tokuda, Yumi Nishiyama, 2006, Phytochemistry.

Co2(CO)8-mediated endo mode cyclization of epoxy-alcohol: synthesis of 2-ethynyl-3-hydroxy-2-methyltetrahydropyran and 2-ethynyl-3-hydroxy-3-methyltetrahydropyran derivatives.

C. Mukai, M. Hanaoka, S. Yamaguchi, 2001, Chemical & pharmaceutical bulletin.

Biomimetic Synthesis of Benzo[C]Phenanthridine Alkaloids from Protoberberines

C. Mukai, M. Hanaoka, 1994 .

Stereoselective Syntheses of (+)-Goniotriol, (+)-8-Acetylgoniotriol, (+)-Goniodiol, (+)-9-Deoxygoniopypyrone, (+)-Altholactone, and (−)-Goniofupyrone

C. Mukai, M. Hanaoka, Syuichi Hirai, 1997 .

First total synthesis and structural elucidation of (−)-goniofupyrone

C. Mukai, M. Hanaoka, I. Kim, 1996 .

Chemical transformation of protoberberines. XVII, Biomimetic introduction of an oxy functionality at the C-10 position in the benzo[c]phenanthridine skeleton : synthesis of 2,3,7,8,10-pentaoxygenated benzo[c]phenanthridine alkaloids, chelilutine and sanguilutine

W. Cho, C. Mukai, M. Hanaoka, 1991 .

A FIRST TOTAL SYNTHESIS OF ()-AMBININE

W. Cho, C. Mukai, M. Hanaoka, 1991 .

Chemical Transformation of Protoberberines. XVI. Regioselective Introduction of an Oxy Functionality at the C12-Position of the Benzo[c]phenanthridine Skeleton : A Convenient Synthesis of Macarpine from Oxychelirubine

W. Cho, C. Mukai, M. Hanaoka, 1990 .

A novel and biomimetic synthesis of chelilutine and sanguilutine.

W. Cho, C. Mukai, M. Hanaoka, 1989 .

A new and convenient synthesis of macarpine and dihydromacarpine from oxychelirubine

W. Cho, C. Mukai, M. Hanaoka, 1989 .

A biomimetic synthesis of (±)-corynoline, (±)-11-epicorynoline, (±)-isocorynoline, and (±)-11-epiisocorynoline from corysamine

C. Mukai, M. Hanaoka, S. Yoshida, 1988 .

Chemical Transformation of Protoberberines. XI. A Novel Synthesis of 2, 3, 10, 11-Tetraoxygenated Protoberberine Alkaloids from Corresponding 2, 3, 9, 10-Tetraoxygenated Protoberberine Alkaloids

M. Marutani, W. Cho, C. Mukai, 1987 .

A new and convenient synthesis of protoberberine alkaloids: (±)-tetrahydropalmatine, (±)-sinactine, (±)-canadine, and (+)-stylopine

M. Hanaoka, S. Yasuda, T. Hirasawa, 1987 .

Chemical transformation of protoberberines. Part 10. A novel synthesis of sanguilutine and dihydrosanguilutine, fully aromatised 2,3,7,8,10-pentaoxygenated benzo[c]phenanthridine alkaloids

C. Mukai, M. Hanaoka, N. Kobayashi, 1987 .

Chemical transformation of protoberberines. Part 9. A biomimetic synthesis of oxychelerythrine, dihydrochelerythrine, and chelerythrine from berberine

C. Mukai, M. Hanaoka, Toshio Motonishi, 1986 .

Synthesis of fagaridine, a phenolic benzo (c) phenanthridine alkaloid.

C. Mukai, H. Yamagishi, M. Hanaoka, 1985 .

Transformation of 2,3,9,10-tetraoxygenated protoberberine alkaloids into 2,3,10,11-tetraoxygenated protoberberine alkaloids

M. Marutani, C. Mukai, M. Hanaoka, 1985 .

A biomimetic conversion of berberine into chelerythrine and dihydrochelerythrine

C. Mukai, M. Hanaoka, Toshio Motonishi, 1984 .

A biomimetic synthesis of (±)-corydalic acid methyl ester from corysamine

C. Mukai, M. Hanaoka, S. Yoshida, 1984 .

Synthetic Studies on Lythraceae Alkaloids. III. Stereoselective Total Synthesis of (±)-Decaline

M. Hanaoka, Y. Arata, N. Ogawa, 1975 .

A novel and stereoselective synthesis of (±)-cephalotaxine and its analogue

Takahiro Yamada, M. Hanaoka, S. Yasuda, 1986 .

1,6-Dihydro-3 (2H)-pyridinones as synthetic intermediates. Formal synthesis of (±)-tabersonine and (±)-catharanthine

T. Imanishi, M. Hanaoka, H. Shin, 1980 .

Causative agent of vascular pain among photodegradation products of dacarbazine

K. Miyamoto, C. Emoto, K. Yokogawa, 2002, The Journal of pharmacy and pharmacology.

Determination of a Pain Substance Produced by the Photodegradation of Dacarbazine

K. Miyamoto, C. Emoto, F. Ichimura, 2001 .

Photochemical valence tautomerization of berberinephenolbetaines to 8,14-cycloberbines, versatile aziridine derivatives for spirobenzylisoquinolines

T. Imanishi, M. Hanaoka, S. Yasuda, 1980 .

Synthesis and gastrointestinal prokinetic activity of novel benzamide derivatives with amphoteric side chains.

T. Saito, H. Kato, M. Hanaoka, 2001, Chemical & pharmaceutical bulletin.

Synthetic Studies on Lythraceae Alkaloids. IV. Total Synthesis of (±)-Methyldecinine

M. Hanaoka, H. Sassa, Y. Arata, 1975 .

A New Synthesis of (±)-Canadaline

T. Imanishi, M. Hanaoka, K. Nagami, 1979 .

A TOTAL SYNTHESIS OF (±)-CEPHALOTAXINAMIDE

M. Hanaoka, S. Yasuda, S. Yoshida, 1988 .

Conversion of Berberine into Benzindanoazepines via 8,14-Cycloberbines

M. Hanaoka, S. Yasuda, K. Nagami, 1982 .

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 .

Chemical transformation of protoberberines. XII A novel synthesis of rhoeadine alkaloids. An alternative synthesis of a key intermediate, benzindenoazepine, for a synthesis of (.+-.)-cis-alpinigenine and (.+-.)-cis-alpinine from palmatine.

M. Hanaoka, N. Kobayashi, S. Yasuda, 1987 .

Chemical transformation of protoberberines. VII. Efficient conversion of protoberberines into benzindenoazepines via 8,14-cycloberbines.

S. Kim, M. Hanaoka, S. Yasuda, 1985, Chemical and pharmaceutical bulletin.

Studies on 1-azabicyclo compounds. XXVII. Synthesis of ten-membered ring amines from 1-oxo-, 9a-benzyl-, and 9a-benzyl-1-oxo-quinolizidine.

M. Hanaoka, S. Yasuda, Y. Arata, 1976 .

Chemical Transformation of Protoberberines. Part 12. A Novel Synthesis of Rhoeadine Alkaloids. An Alternative Synthesis of a Key Intermediate, Benzindenoazepine, for a Synthesis of (.+-.)-cis-Alpinigenine and (.+-.)-cis- Alpinine from

M. Hanaoka, N. Kobayashi, S. Yasuda, 1987 .

Efficient conversion of protoberberines into benzindenoazepines. A formal synthesis of (.+-.)-cis-alpinigenine and (.+-.)-cis-alpinine.

S. Sakurai, M. Hanaoka, S. Yasuda, 1982 .

A FIRST AND STEREOSELECTIVE SYNTHESIS OF (±)-RADDEANAMINE

M. Hanaoka, S. Yasuda, Masumi Kohzu, 1985 .

CHEMICAL TRANSFORMATION OF PROTOBERBERINES. VII. EFFICIENT CONVERSION OF PROTOBERBERINES INTO BENZINDENOAZEPINES VIA 8,14-CYCLOBERBINES

S. Kim, M. Hanaoka, S. Yasuda, 1985 .

Revised Structure of Gonioheptolide A

C. Mukai, J. McLaughlin, M. Hanaoka, 1999 .

1, 6-DIHYDRO-3 (2H)-PYRIDINONES AS SYNTHETIC INTERMEDIATES. STEREOSELECTIVE SYNTHESIS OF (±)-CORYNANTHEIDOL AND (±)-QUININE

T. Imanishi, M. Inoue, M. Hanaoka, 1982 .

Highly stereocontrolled total synthesis of (+)-bengamide E

C. Mukai, M. Hanaoka, O. Kataoka, 1995 .