柴崎正勝
Shibasaki, Masakatsu, 1947-....
Shibasaki, Masakatsu
柴崎, 正勝, 1947-
시바사키 마사카쓰 1947-
柴崎, 正勝
Shibasaki, Masakatsu, farmaceut
VIAF ID: 3550260 (Personal)
Permalink: http://viaf.org/viaf/3550260
Preferred Forms
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- 100 1 _ ‡a Shibasaki, Masakatsu
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- 100 1 _ ‡a Shibasaki, Masakatsu ‡d 1947-
- 100 1 _ ‡a Shibasaki, Masakatsu ‡d 1947-
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- 100 1 _ ‡a Shibasaki, Masakatsu, ‡d 1947-....
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- 100 1 _ ‡a 柴崎, 正勝
- 100 1 _ ‡a 柴崎, 正勝, ‡d 1947-
- 100 0 _ ‡a 柴崎正勝
- 100 1 _ ‡a 시바사키 마사카쓰 ‡d 1947-
4xx's: Alternate Name Forms (31)
Works
Title | Sources |
---|---|
Bifunctional molecular catalysis | |
Bunseki kagaku. | |
Catalytic methods : C-C bond formation | |
Chembiomolecular Science. At the Frontier of Chemistry and Biology | |
Comprehensive chirality | |
Daigakuin kōgi yūki kagaku. | |
Dramatic switching of protein kinase C agonist/antagonist activity by modifying the 12-ester side chain of phorbol esters | |
Efficient synthesis of antihyperglycemic | |
Efficient two-step conversion of alpha,beta-unsaturated aldehydes to optically active gamma-oxy-alpha,beta-unsaturated nitriles and its application to the total synthesis of (+)-patulolide C | |
Electrophilic Activation of α,β-Unsaturated Amides: Catalytic Asymmetric Vinylogous Conjugate Addition of Unsaturated γ-Butyrolactones | |
Enantio- and diastereoselective catalytic Mannich-type reaction of a glycine schiff base using a chiral two-center phase-transfer catalyst. | |
Enantioselective Ring Opening of Epoxides with 4-Methoxyphenol Catalyzed by Gallium Heterobimetallic Complexes: An Efficient Method for the Synthesis of Optically Active 1,2-Diol Monoethers | |
Enantioselective syntheses of aeruginosin 298-A and its analogues using a catalytic asymmetric phase-transfer reaction and epoxidation | |
Enantioselective Total Synthesis of (−)-Strychnine Using the Catalytic Asymmetric Michael Reaction and Tandem Cyclization [J. Am. Chem. Soc.2002,124, 14546−14547]. | |
Highly enantioselective catalytic Michael reaction of α-substituted malonates using La-linked-BINOL complex in the presence of HFIP (1,1,1,3,3,3-hexafluoroisopropanol) | |
In situ manipulation of catalyst performance via the photocontrolled aggregation/dissociation state of the catalyst | |
An introduction medicinal chemistry. | |
Iyakuhin johogaku. | |
Iyakuhin kaihatsuron | |
Jitsumu jisshū jizen gakushū no tameno chōzaigaku | |
Kagaku kōzō to yakuri sayō : Iyakuhin o kagakuteki ni yomu | |
Ligand accelerated indium(iii)-catalyzed asymmetric alkynylation of aldehydes with 2-methyl-3-butyn-2-ol as an ethyne equivalent donor | |
Linking structural dynamics and functional diversity in asymmetric catalysis. | |
Managing the retro-pathway in direct catalytic asymmetric aldol reactions of thioamides | |
Medishinaru kemisutorī | |
Multimetallic catalysts in organic synthesis | |
Neighboring Protonation Unveils Lewis Acidity in the B3NO2 Heterocycle | |
A New and Highly Efficient Asymmetric Route to Cyclic α-Amino Phosphonates: The First Catalytic Enantioselective Hydrophosphonylation of Cyclic Imines Catalyzed by Chiral Heterobimetallic Lanthanoid Complexes | |
New entries in Lewis acid-Lewis base bifunctional asymmetric catalyst: catalytic enantioselective Reissert reaction of pyridine derivatives. | |
A New Entry in Catalytic Alkynylation of Aldehydes and Ketones: Dual Activation of Soft Nucleophiles and Hard Electrophiles by an Indium | |
On the Role of Silver Salts in Asymmetric Heck-type Reaction. A Greatly Improved Catalytic Asymmetric Synthesis ofcis-Decalin Derivatives | |
Organic chemistry. | |
Oseltamivir enhances hippocampal network synchronization | |
P-glycoprotein restricts the penetration of oseltamivir across the blood-brain barrier. | |
Raifu saiensu o shikoshita yuki gosei. | |
Sc3+-catalyzed aldol-type additions of N-benzoylcyclopropanecarboxamides via iodide-mediated ring-opening: stereoselective synthesis of gamma-lactams | |
Self-assembling neodymium/sodium heterobimetallic asymmetric catalyst confined in a carbon nanotube network. | |
Sequential regulation of DOCK2 dynamics by two phospholipids during neutrophil chemotaxis. | |
Sequential Wittig olefination-catalytic asymmetric epoxidation with reuse of waste Ph3P(O): application of alpha,beta-unsaturated N-acyl pyrroles as ester surrogates. | |
Short synthesis of (+)-cylindricine C by using a catalytic asymmetric Michael reaction with a two-center organocatalyst | |
Solvent-Dependent Enantiodivergence in anti-Selective Catalytic Asymmetric Nitroaldol Reactions | |
Solvent-dependent self-discrimination of bis(2-hydroxyphenyl)diamides | |
Sōyaku kagaku no kiso to naru fusei hannō. | |
Sōyaku kagaku no miryoku : Tōkyō daigaku daigakuin yakugakukei kenkyūka kara no hasshin | |
Stimulating concepts in chemistry | |
Strategy for enantio- and diastereoselective syntheses of all possible stereoisomers of 1,3-polyol arrays based on a highly catalyst-controlled epoxidation of alpha,beta-unsaturated morpholinyl amides: application to natural product synthesis | |
Studies on catalytic enantioselective total synthesis of caprazamycin B: construction of the western zone | |
Studies toward the total synthesis of garsubellin A: a concise synthesis of the 18-epi-tricyclic core | |
syn-Selective catalytic asymmetric 1,4-addition of alpha-ketoanilides to nitroalkenes under dinuclear nickel catalysis. | |
syn-Selective catalytic asymmetric nitro-Mannich reactions using a heterobimetallic Cu-Sm-Schiff base complex | |
Synthesis of Androprostamine A and Resormycin. | |
Synthesis of Unprotected Spirocyclic β-Prolines and β-Homoprolines by Rh-Catalyzed C-H Insertion | |
Total synthesis of lactacystin and salinosporamide A. | |
Trichloromethyl ketones as synthetically versatile donors: application in direct catalytic mannich-type reactions and the stereoselective synthesis of azetidines. | |
TriQuinoline | |
Unique physicochemical and catalytic properties dictated by the B3NO2 ring system | |
Unique reactivity of alpha,beta-unsaturated carboxylic acid imidazolides: catalytic asymmetric synthesis of alpha,beta-epoxy esters and alpha,beta-epoxy carboxylic acid derivatives | |
Yakubutsu dōtaigaku | |
Yūki kagaku : Seitai hannō eno apurōchi | |
α-Halo Amides as Competent Latent Enolates: Direct Catalytic Asymmetric Mannich-Type Reaction. | |
ライフサイエンスを志向した有機合成 | |
分析化学. | |
創薬化学の基礎となる不斉反応 | |
創薬指向の分子設計 : 基礎と展開 | |
創薬科学の魅力 : 東京大学大学院薬学系研究科からの発信 | |
製剤学・物理薬剤学 | |
化学構造と薬理作用 : 医薬品を化学的に読む | |
医薬品開発論 | |
医薬品情報学 | |
四級炭素の触媒的不斉構築を基軸とする有用物資の全合成に関する研究 | |
地球環境と有機合成 | |
大学院講義有機化学. | |
実務実習事前学習のための調剤学 | |
新しい概念に基づく不斉触媒の創製と医薬関連物質合成への展開 | |
新医薬品の創製をめざしたホモイソカルバサイクリンの化学合成 | |
新規触媒的不斉アルドール反応の開発と応用 | |
有機分子触媒の新展開 = New development of organocatalyst | |
有機化学 : 生体反応へのアプローチ | |
薬物動態学 | |
触媒的不斉炭素‐炭素結合生成反応を基盤とした有用生物活性物質の合成研究 | |
革新的不斉触媒の最適化と新たな展開 |