Highly enantioselective mukaiyama aldol reaction of alpha,alpha-dichloro ketene silyl acetal: an efficient synthesis of a key intermediate for diltiazem.
about
Reduction of 2,2,2-trichloro-1-arylethanones by RMgX: mechanistic investigation and the synthesis of substituted α,α-dichloroketones.Highly efficient asymmetric synthesis of α,β-epoxy esters via one-pot organocatalytic epoxidation and oxidative esterification.Grignard-mediated reduction of 2,2,2-trichloro-1-arylethanones
P2860
Highly enantioselective mukaiyama aldol reaction of alpha,alpha-dichloro ketene silyl acetal: an efficient synthesis of a key intermediate for diltiazem.
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年學術文章
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2003年學術文章
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2003年學術文章
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name
Highly enantioselective mukaiy ...... ey intermediate for diltiazem.
@en
Highly enantioselective mukaiy ...... ey intermediate for diltiazem.
@nl
type
label
Highly enantioselective mukaiy ...... ey intermediate for diltiazem.
@en
Highly enantioselective mukaiy ...... ey intermediate for diltiazem.
@nl
prefLabel
Highly enantioselective mukaiy ...... ey intermediate for diltiazem.
@en
Highly enantioselective mukaiy ...... ey intermediate for diltiazem.
@nl
P356
P1476
Highly enantioselective mukaiy ...... ey intermediate for diltiazem.
@en
P2093
Ritsuo Imashiro
Tooru Kuroda
P304
P356
10.1021/JO026361+
P407
P577
2003-02-01T00:00:00Z