浅岡守夫 (Morio Asaoka) - マイポータル

基本情報

学位: 理学博士

J-GLOBAL ID: 200901018430513057
researchmap会員ID: 1000015814

研究キーワード

研究分野

経歴

日本女子大学理学部物質生物科学科, 教授

学歴

MISC

Synthesis of Ketones from Carboxylic Acids with R(PrNH)Mg

Maria Ohki, Morio Asaoka

CHEMISTRY LETTERS 38(8) 856-857 2009年8月
Enantioselective total synthesis of (+)-sarcodictyenone

Takako Yamazaki, Minoru Ishikawa, Miki Uemura, Yuko Kanda, Hisashi Takei, Morio Asaoka

TETRAHEDRON 64(8) 1895-1900 2008年2月
Conjugate Addition of RMgX-3MeLi to a,b-Unsaturated Amides and a,b-Unsaturated Carboxylic Acids

M. Kikuchi, S. Niikura, N. Chiba, N. Terauchi, M. Asaoka

Chemistry Letteres 36(6) 736 2007年
Conjugate Addition of RMgX-3MeLi to a,b-Unsaturated Amides and a,b-Unsaturated Carboxylic Acids

M. Kikuchi, S. Niikura, N. Chiba, N. Terauchi, M. Asaoka

Chemistry Letteres 36(6) 736 2007年
"contra-Michael" addition of alkyllithiums to silicon- and phenyl-substituted alpha,beta-unsaturated amides in the presence of t-BuOK

Tomoko Hinago, Nana Teshima, Satoko Kenmoku, Tiyako Kamata, Nahoko Terauchi, Nao Chiba, Chikako Satoh, Aya Nakamura, Morio Asaoka

CHEMISTRY LETTERS 36(1) 54-55 2007年1月
Formation of 3-Pyrrolin-2-ones via 5-Endo-Trig Cyclization

R. Naitoh, Y. Nakamura, E. Katano, Y. Nakamura, E. Okada, M. Asaoka

Heterocycles 63(5) 1009 2004年
Formation of 3-Pyrrolin-2-ones via 5-Endo-Trig Cyclization

R. Naitoh, Y. Nakamura, E. Katano, Y. Nakamura, E. Okada, M. Asaoka

Heterocycles 63(5) 1009 2004年
Diastereoselective reactions of a homoenolate generated from (S)-N-(1-phenylethyl)-3-(trimethylsilyl)propanamide: Enantioselective synthesis of (+)-massoialactone

N Sadayori, A Kawatoh, R Sakurazawa, T Utsumi, M Inagaki, M Asaoka

HETEROCYCLES 58 191-202 2002年11月
Diastereoselective Reactons of a Homoenolate Generated from 3-(Trimethylsilyl)propanamide: Enantioselective Synthesis of (+)-Massoialactone

N. Sadayori, A. Kawatoh, R. Sakurazawa, T. Utsumi, M. Inagaki, M. Asaoka

Heterocycles 58 191 2000年
Highly Diastereoselective Reduction of γ-Keto Amides: Diastereoselective Synthesis of γ－Butyrolactones with Contiguous Chiral Centers

M. Satoh, S. Washida, S. Takeuchi, M. Asaoka

Heterocycles 52(1) 227-236 2000年1月
Diastereoselective Reactons of a Homoenolate Generated from 3-(Trimethylsilyl)propanamide: Enantioselective Synthesis of (+)-Massoialactone

N. Sadayori, A. Kawatoh, R. Sakurazawa, T. Utsumi, M. Inagaki, M. Asaoka

Heterocycles 58 191 2000年
Highly diastereoselective reduction of gamma-keto amides: Diastereoselective synthesis of gamma-butyrolactones with contiguous chiral centers

M Satoh, S Washida, S Takeuchi, M Asaoka

HETEROCYCLES 52(1) 227-236 2000年1月
Generation of Silyl Group Stabilized Amide Homoenolates by Utilizing the Complex-Induced Proximity Effect(CIPE)

T. shinozuka, T. Utsumi, M. Inagaki, M. Asaoka

Journal of the Chemical Society Perkin Transactions 1 2433 1999年
A New Synthesis of (+)-Bakuchiol

S. Sakakiyama, K. Yamamoto, M. Asaoka

Natural Product Letters 14(1) 1 1999年
Generation of Silyl Group Stabilized Amide Homoenolates by Utilizing the Complex-Induced Proximity Effect(CIPE)

T. shinozuka, T. Utsumi, M. Inagaki, M. Asaoka

Journal of the Chemical Society Perkin Transactions 1 2433 1999年
A New Synthesis of (+)-Bakuchiol

S. Sakakiyama, K. Yamamoto, M. Asaoka

Natural Product Letters 14(1) 1 1999年
Diastereodivergency in the reactions of 3-metallated-2-methylbutanamide

Morio Asaoka, Michiko Tanaka, Takashi Houkawa, Tsuyoshi Ueda, Satoshi Sakami, Hisashi Takei

Tetrahedron 54(3-4) 471-486 1998年1月15日
Stereoselective Reactions of α-(Arylsulfomyl)cyclohexyl Carbanions

M. Tanaka, M. Nakatani, M. Asaoka

Journal of the Chemical Society Perkin Transactions 1 3519 1998年
Diastereodivergency in the reactions of 3-metallated-2-methylbutanamide

M Asaoka, M Tanaka, T Houkawa, T Ueda, S Sakami, H Takei

TETRAHEDRON 54(3-4) 471-486 1998年1月
Stereoselective Reactions of α-(Arylsulfomyl)cyclohexyl Carbanions

M. Tanaka, M. Nakatani, M. Asaoka

Journal of the Chemical Society Perkin Transactions 1 3519 1998年

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浅岡守夫

基本情報

研究キーワード

研究分野

経歴

学歴

MISC

所属学協会

共同研究・競争的資金等の研究課題

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