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The Chiral Pool in the Pictet-Spengler Reaction for the Synthesis of β-CarbolinesTransition-metal-catalyzed C-H bond functionalizations: feasible access to a diversity-oriented β-carboline library.Total synthesis of (+)-sieboldine a: evolution of a pinacol-terminated cyclization strategy.Methods for direct alkene diamination, new & old.Total synthesis of (+)-sieboldine A.Weak Brønsted acid-thiourea co-catalysis: enantioselective, catalytic protio-Pictet-Spengler reactions.Preparation of functionalized indoles and azaindoles by the intramolecular copper-mediated carbomagnesiation of ynamides.Reactivity of 4-tert-butyldimethylsiloxy-1,2,3,6-tetrahydropyridines with hydrazines.Chiral Thioureas Promote Enantioselective Pictet-Spengler Cyclization by Stabilizing Every Intermediate and Transition State in the Carboxylic Acid-Catalyzed Reaction.Two-step synthesis of multi-substituted amines by using an N-methoxy group as a reactivity control element.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
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2005年學術文章
@zh-hant
name
Stereocontrolled total synthesis of (-)-eudistomin C.
@en
type
label
Stereocontrolled total synthesis of (-)-eudistomin C.
@en
prefLabel
Stereocontrolled total synthesis of (-)-eudistomin C.
@en
P2093
P356
P1476
Stereocontrolled total synthesis of (-)-eudistomin C.
@en
P2093
Hidetoshi Tokuyama
Nobutaka Kawai
Tohru Fukuyama
Tohru Yamashita
P304
15038-15039
P356
10.1021/JA055832H
P407
P577
2005-11-01T00:00:00Z