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Stereoselective intramoleculer allylsilane additions to chiral aldehydes
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title
Stereoselective intramoleculer allylsilane additions to chiral aldehydes
(English)
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main subject
stereoselectivity
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based on heuristic
inferred from title
chirality
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inferred from title
author
Carsten Bolm
object named as
C. Bolm
series ordinal
3
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author name string
M.T. Reetz
series ordinal
1
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A. Jung
series ordinal
2
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publication date
January 1988
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published in
Tetrahedron
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volume
44
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issue
13
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page(s)
3889-3898
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cites work
Stereoselective aldol additions to α-alkoxy aldehydes using thioester silyl ketene acetals,
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reference URL
https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2986643-6
retrieved
7 January 2021
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Lewis acid promoted aldol additions of α-thiosilylketeneacetals to α-alkoxy aldehydes: diastereoselective synthesis of -α-methylene-β-hydroxy-∂-alkoxy esters
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reference URL
https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2986643-6
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7 January 2021
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Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis
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reference URL
https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2986643-6
retrieved
7 January 2021
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Allyldimethylsilyl ethers. New derivatives for the analysis of steroids by gas chromatography-mass spectrometry
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https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2986643-6
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7 January 2021
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On the origins of stereoselectivity in chelation controlled nucleophilic additions to .beta.-alkoxy aldehydes: solution structures of Lewis acid complexes via NMR spectroscopy
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reference URL
https://api.crossref.org/works/10.1016%2FS0040-4020%2801%2986643-6
retrieved
7 January 2021
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Identifiers
DOI
10.1016/S0040-4020(01)86643-6
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