Asymmetric total synthesis of (+)-brefeldin A from (S)-lactate by triple chirality transfer process and nitrile oxide cycloaddition.
about
trans-Hydrogenation: application to a concise and scalable synthesis of brefeldin AEasy and direct conversion of tosylates and mesylates into nitroalkanes.Transition structures of diastereoselective 1,3-dipolar cycloadditions of nitrile oxides to chiral homoallylic alcohols.Cascade reactions: a driving force in akuammiline alkaloid total synthesis.trans-Hydrogenation: Application to a Concise and Scalable Synthesis of Brefeldin AFormal synthesis of (+)-brefeldin A: application of a zinc-mediated ring expansion reaction.Uncommon 1,2-Migration of a Nitro Group Within a β-Nitrostyryl Moiety: Synthetic Scope and Mechanistic Details
P2860
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P2860
Asymmetric total synthesis of (+)-brefeldin A from (S)-lactate by triple chirality transfer process and nitrile oxide cycloaddition.
description
2002 nî lūn-bûn
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2002年の論文
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2002年学术文章
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2002年学术文章
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name
Asymmetric total synthesis of ...... d nitrile oxide cycloaddition.
@en
type
label
Asymmetric total synthesis of ...... d nitrile oxide cycloaddition.
@en
prefLabel
Asymmetric total synthesis of ...... d nitrile oxide cycloaddition.
@en
P2093
P356
P1476
Asymmetric total synthesis of ...... d nitrile oxide cycloaddition.
@en
P2093
Deukjoon Kim
Jongkook Lee
Joong Inn Lim
Phil Jong Shim
Sanghee Kim
P304
P356
10.1021/JO010743I
P407
P577
2002-02-01T00:00:00Z