Super silyl stereo-directing groups for complete 1,5-syn and -anti stereoselectivities in the aldol reactions of beta-siloxy methyl ketones with aldehydes.
about
Ten years of research in Chicago.Rapid, one-pot synthesis of β-siloxy-α-haloaldehydes.The supersilyl group as a carboxylic acid protecting group: application to highly stereoselective aldol and Mannich reactions.Rapid total syntheses utilizing "supersilyl" chemistry.β-Siloxy-α-haloketones through highly diastereoselective single and double mukaiyama aldol reactions.Stereodivergent approach to the avermectins based on "super silyl" directed aldol reactionsRapid and stereochemically flexible synthesis of polypropionates: super-silyl-governed aldol cascades.Synthesis of β-hydroxy-α-haloesters through super silyl ester directed syn-selective aldol reaction.Generation of organolithium compounds bearing super silyl ester and their application to Matteson rearrangement.Stereoselective synthesis of multiple stereocenters by using a double aldol reaction.Regioselective chromatic orthogonality with light-activated metathesis catalysts.
P2860
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P2860
Super silyl stereo-directing groups for complete 1,5-syn and -anti stereoselectivities in the aldol reactions of beta-siloxy methyl ketones with aldehydes.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年學術文章
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2010年學術文章
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2010年學術文章
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name
Super silyl stereo-directing g ...... methyl ketones with aldehydes.
@en
type
label
Super silyl stereo-directing g ...... methyl ketones with aldehydes.
@en
prefLabel
Super silyl stereo-directing g ...... methyl ketones with aldehydes.
@en
P2860
P356
P1476
Super silyl stereo-directing g ...... methyl ketones with aldehydes.
@en
P2093
Hisashi Yamamoto
Yousuke Yamaoka
P2860
P304
P356
10.1021/JA101076Q
P407
P577
2010-04-01T00:00:00Z