正木 幸雄 | 岐阜薬科大学

スポンサーリンク

概要

• 同名の論文著者
• 岐阜薬科大学の論文著者

関連著者

• 正木 幸雄

  岐阜薬科大学

• 正木 幸雄

  Gifu Pharmaceutical University

• MASAKI Yukio

  Gifu Pharmaceutical University

• ITOH Akichika

  Gifu Pharmaceutical University

• Kodama T

  Gifu Pharmaceutical University

• Ochiai Masahito

  Institute For Chemical Research Kyoto University

• 正木 幸雄

  岐阜薬科大学:(現)名城大学薬学部薬化学教室

• Inagaki S

  Toyota Central R & D Laboratories Inc.

• 伊藤 彰近

  岐阜薬科大学創薬化学大講座合成薬品製造学研究室

• 伊藤 彰近

  岐阜薬科大学

• Oda Hirohisa

  Gifu Pharmaceutical University

• Shiro M

  Rigaku Corp. Tokyo

• OCHIAI Masahito

  Faculty of Pharmaceutical Sciences, University of Tokushima

• 落合 正仁

  Faculty Of Pharmaceutical Sciences University Of Tokushima

• Shiro M

  Rigaku Corporation

• Itoh Akichika

  Gifu Pharmaceutical Univ.

• KODAMA Tomohiro

  Gifu Pharmaceutical University

• MIURA Tsuyoshi

  Gifu Pharmaceutical University

• MIZUNO Kazuhiro

  Gifu Pharmaceutical University

• 冨士 薫

  Institute For Chemical Research Kyoto University

• 小田 博久

  Gifu Pharmaceutical University

• ARASAKI Hideki

  Gifu Pharmaceutical University

• Node Manabu

  Department Of Pharmaceutical Manufacturing Chemistry 21st Century Coe Program Kyoto Pharmaceutical U

• Node Manabu

  Kyoto Pharmaceutical Univ.

• Suzuki Mitsuko

  Institute For Chemical Research Kyoto University

• Node Manabu

  Department Of Pharmaceutical Manufacturing Chemistry 21st Century Coe Program Kyoto Pharmaceutical U

• SHINOZAKI Katsuo

  Gifu Pharmaceutical University

• INAGAKI Shinji

  Toyota Central R&D Laboratories, Inc.

• SHIRO Motoo

  Rigaku Corporation X-ray Research Laboratory

• Inagaki Shinji

  Toyota Central R & D Laboratories Inc.

• 伊藤 彰近

  岐阜薬大

• 正木 幸雄

  岐阜薬大

• Yanagida S

  Osaka Univ. Osaka

• 伊藤 彰近

  岐阜薬科大学合成薬品製造学教室

• TANAKA Nobuyuki

  Gifu Pharmaceutical University

• Iwata M

  Gifu Pharmaceutical University

• Yanagida Shozo

  Department Of Biotechnology Department Of Material & Life Science Graduate School Of Engineering

• Pac Chyongjin

  Kawamura Institute Of Chemical Research

• OCHIAI Masahito

  Gifu Pharmaceutical University

• Shiro Motoo

  Rigaku Co.

• MASAKI Yasuhiro

  Department of Chemical Process Engineering, Faculty of Engineering, Osaka University

• Mito S

  Institute For Chemical Research Kyoto University

• Yanagida Shozo

  Department of Applied Chemistry, Faculty of Engineering, Osaka University

• 野出 学

  Kyoto Pharmaceutical University

• 野出 学

  Institute For Chemical Research Kyoto University

• 長島 弘

  Gifu Pharmaceutical University

• 冨士 薫

  京都大学化学研究所

• 川端 猛夫

  京都大学化学研究所

• OSHIMA Kunio

  Gifu Pharmaceutical University

• 〓 小江

  京大・化研

• 冨士 薫

  京大・化研

• 〓 小江

  Institute For Chemical Research Kyoto University

• 川端 猛夫

  京大・化研

• 大森 富士海

  京大・化研

• 野出 学

  京都薬大

• 児玉 朋寛

  岐阜薬科大学合成薬品製造学教室

• 三浦 剛

  Gifu Pharmaceutical University

• 向井 功

  Gifu Pharmaceutical University

• 岩田 郁弘

  Gifu Pharmaceutical University

• 伊藤 彰近

  Gifu Pharmaceutical University

• IWATA Masashi

  Gifu Pharmaceutical University

• MAKIDA Miyuki

  Gifu Pharmaceutical University

• 今枝 稔博

  Gifu Pharmaceutical University

• 小田 博久

  岐阜薬科大学

• 長島 弘

  岐阜薬科大学

• 今枝 稔博

  岐阜薬大

• 小田 博久

  岐阜薬大

• 川端 猛夫

  京大化研

• 大森 富士海

  Institute For Chemical Research Kyoto University

• 正木 幸雄

  岐阜薬科大学合成薬品製造学教室

• IMAEDA Toshihiro

  Gifu Pharmaceutical University

• Masuoka S

  Takara Agri Co. Ltd.

• Ochiai Masahito

  Faculty Of Pharmaceutical Sciences University Of Tokushima

• Shiro Motoo

  Shionogi Research Laboratry Shionogi & Co. Ltd.

• SHINOZAKI Katsuo

  (Present address)Central Research Laboratories, Zeria Pharmaceutical Co., Ltd.,

• WAKAMATSU Hideaki

  Gifu Pharmaceutical University

• MIYAKE Kunihito

  Department of Chemical Process Engineering, Faculty of Engineering, Osaka University

• UEHARA Yoshikazu

  Department of Chemical Process Engineering, Faculty of Engineering, Osaka University

• Miyake Kunihito

  Department Of Chemical Process Engineering Faculty Of Engineering Osaka University

• Uehara Yoshikazu

  Department Of Chemical Process Engineering Faculty Of Engineering Osaka University

もっと見る 閉じる

著作論文

• メソポーラスシリカを活用する有機合成反応の開発に関する研究
• 不斉二級アルコール誘導体とジクロロカルベンの立体特異的C-H挿入反応を経る不斉四級炭素の構築
• 16 不斉ニトロオレフィン化反応を鍵反応とする光学活性フィゾスチグミンの合成(口頭発表の部)
• Tetracyanoethylene-Hydrogen Peroxide, a Mild Epoxidation System of Olefins
• Oxidative Photo-Decarboxylation in the Presence of Mesoporous Silicas
• Oxidative Transformation of Arylmethyl Bromides and Alcohols with a Combination of Mesoporous Silica FSM-16 and Alkali Iodides under Photoirradiation.
• Photooxidation of Arylmethyl Bromides with Mesoporous Silica FSM-16.
• New Synthetic Method of Imides through Oxidative Photodecarboxylation Reaction of N-Protected α-Amino Acids with FSM-16.
• Oxidative Photodecarboxylation of α-Hydroxycarboxylic Acids and Phenylacetic Acid Derivatives with FSM-16.
• New Synthetic Method of Imides through Oxidative Photodecarboxylation Reaction of N-Protected α-Amino Acids with FSM-16
• Synthesis of (R)-(+)-Tanikolide through Stereospecific C-H Insertion Reaction of Dichlorocarbene with Optically Active Secondary Alcohol Derivatives
• Stereospecific Construction of Chiral Quaternary Carbon Compounds from Chiral Secondary Alcohol Derivatives
• 研究開発情報 メソポーラスシリカを利用する有機合成反応
• Polymer-Supported Dicyanoketene Acetal as a π-Acid Catalyst : Monothioacetalization and Carbon-Carbon Bond Formation of Acetals.
• Polymer-Supported Dicyanoketene Acetal as a π-Acid Catalyst : Monothioacetalization and Carbon-Carbon Bond Formation of Acetals
• Unprecedented Polymer-supported π-Acid : Synthesis and Its Application as a Promoter to the Monothioacetalization of Acetals.
• Mild Esterification and Transesterification of Carboxylic Acids Catalyzed by Tetracyanoethylene and Dicyanoketene Dimethyl Acetal
• Mild Esterification and Transesterification of Carboxylic Acids Catalyzed by Tetracyanoethylene and Dicyanoketene Dimetheyl Acetal
• Pyridazino〔4,5-e〕-1,2,4-triazineの誘導体の合成と除草作用
• メソポーラスシリカを利用する有機合成反応
• 26 酒石酸を不斉源とする(+)-アスペルリンの全合成(口頭発表の部)
• 高分子π酸触媒の開発
• Hard Acid and Soft Nucleophile Systems. Part 12. : Regioselective Functionalization of 1,3-Dienes through the Lewis Acid Mediated Thienium Cation Diels-Alder Reaction.
• Facile Synthesis of Optically Active Tertiary Alcohol Building Blocks by Stereospecific C-H Insertion Reaction of Dichlorocarbene with Secondary Alcohol Derivatives.
• Facile Synthesis of Optically Active Tertiary Alcohol Building Blocks by Stereospecific C - H Insertion Reaction of Dichlorocarbene with Secondary Alcohol Derivatives
• Total Synthesis of (+)-Asperlin Starting with (S, S)-Tartaric Acid.
• Total Synthesis of (+)-Asperlin Starting with (S,S)-Tartaric Acid
• Addition-Elimination Strategy for Asymmetric Induction : A Chiral Sulfoxide as a Leaving Group.
• Deprotection of a Silyl Group with Mesoporous Silica
• New Synthetic Method of Benzaldehydes and α, β-Unsaturated Aldehydes with I_2under Photoirradiation.
• New Synthetic Method of Benzaldehydes and α,β-Unsaturated Aldehydes with I_2 under Photoirradiation
• Selective Deprotection of Triethylsilyl Group in the Presence of t-Butyldimethylsilyl Group with MCM-41/MeOH Heterogeneous System.
• Selective Acceleration for Deprotection of Benzyl Ethers with Ti-HMS
• Short-Step Synthesis of Chiral C_2-Symmetric 2,3,4,5-Tetrasubstituted Pyrrolidines from D-Mannitol and Their Use as Chiral Ligands in the Reaction of Diethylzinc and Benzaldehyde.
• Alcoholysis of Epoxides Catalyzed by Tetracyanoethylene and Dicyanoketene Acetals.
• Alocoholysis of Epoxides Catalyzed by Tetracyanoethylene and Dicyanoketene Acetals
• Alcoholysis of Epoxides Catalyzed by Tetracyanoethylene
• Substrate-Specific Rearrangement and Acetonidation of Epoxy-Ethers Catalyzed by Tetracyanoethylen
• Substrate-Specific Rearrangement and Acetonidation of Epoxy-Ethers Catalyzed by Tetracyanoethylene
• α-Versus β-Elimination of (Z)-(β-Halovinyl)iododinium Salts : Generation of(α-Alkylidene)carbenes and Their Facile Intramolecular 1,2-Migration
• Michael Type Addition of Halides to Alkynyl(phenyl)iodonium Tetrafluoroborates. : Stereoselective Synthesis of (Z)-β-Halovinyl(phenyl)-iodonium Halides.
• Synthesis of (Z)-1,2-Dihalo-1-alkenes by the Reaction of (Z)-(β-Halovinyl)phenyliodonium Salts with n-Bu4NX or KX/CuX. Competitions between Nucleophilic Vinylic Substitutions and Aromatic Substitutions
• Synthesis of (Z)-1,2-Dihalo-1-alkenes by the Reaction of (Z)-(β-Halovinyl)phenyliodonium Salts with n-Bu_4NX or KX/CuX. : Competitions between Nucleophilic Vinylic Substitutions and Aromatic Substitutions.
• Nucleohilic Vinylic Substitutions of (Z)-(β-(Phenylsulfonyl)alkenyl) iodonium Tetrafluoroborates with Sodium Benzenesulfinate : Stereoselective Synthesis of (Z)-1,2-Bis(Phenylsulfonyl)alkenes
• Stereoselective Synthesis of Highly Labile(Z)-β-Alkylvinyl(phenyl) iodonium Perchlorates.
• Nucleophilic Vinylic Substitutions of (Z)-(β-(Phenylsulfonyl)alkenyl)-iodonium Tetrafluoroborates with Tetrabutylammonium Halides : Retention of Configuration.
• Synthesis and Structure of 1-(Diacetoxyiodo)-2,4,6-tri-tert-butylbenzen and Its Analogues.
• Inversion of Configuration in Nucleophilic Vinylic Substitutions of (E)-β-Alkylvinyliodonium Tetrafluoroborates with Halides.
• A Total Synthesis of (-)-Physostigmine.
• Tetracyanoethylene-Hydrogen Peroxide, a Mild Epoxidation System of Olefins.
• Enantiospecific Synthesis of Optically Active Natural (+)-Conhydrine from (S, S)-Tartaric Acid.
• P-Anisyloxymethyl Group, a Novel Oxidatively Removable Acetal Type OH-Protecting Group.
• Synthesis of (3S, 4S)-Statine and a Related Compound, (3S, 4S)-AHPPA, from D-Glucosamine as a Chiral Pool.
• Synthesis of (3S,4S)-Statine and a Related Compound, (3S,4S)-AHPPA, from _D-Glucosamine as a Chiral Pool
• Enantiospecific Synthesis of (3S, 4S)-Statine and Its Analogue from D-Glucosamine as a Chiral Pool.
• Enantiospecific Synthesis of (3S, 4S)-Statine and Its Analogue from D-Glucosamine as a Chiral Pool
• Chiral Synthesis of Dihydroxyamino Acid Moieties of AI-77-B and Calyculins from D-Glucosamine.
• Synthesis of D-erythro-Sphingosine from D-Glucosamine.
• Synthesis of Optically Active, Unusual, and Biologically Important Hydroxy-amino Acids from D-Glucosamine.
• Chiral Syntheses of Dihydroxyamino Acid Moieties of AI-77-B and Calyculins from D-Glucosamine
• Synthesis of D-erythro-Sphingosine from D-Glucosamine
• Participation of a Chain Mechanism in Efficient Monomerization of Dimethylthymine Cyclobutane Dimer Photosensitized by a Flavin in the Presence of Perchloric Acid
• Emissive Triplex Formation in a Methylene-Bridged A-D-D' System. Intramolecular Long-Range Electron Transfer^1

もっと見る 閉じる

スポンサーリンク