1,2-diastereoselection induced by chiral silicon in the addition of Grignard reagents to acylsilanes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
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2. High diastereofacial selectivity in nucleophilic additions to chiral acylsilanes
3. Asymmetric induction by chiral silicon. Synthesis and electrophilic reactivity towards dienes and carbanions of R-(–)-methyl-α-naphthyl-phenylsilyl phenyl thioketone
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1. Changing the Reaction Pathway of Silyl-Prins Cyclization by Switching the Lewis Acid: Application to the Synthesis of an Antinociceptive Compound;The Journal of Organic Chemistry;2023-05-23
2. Chiral Organosilicon Compounds;Organosilicon Compounds;2017
3. The recent synthesis and application of silicon-stereogenic silanes: A renewed and significant challenge in asymmetric synthesis;Chem. Soc. Rev.;2011
4. ChemInform Abstract: 1,2-Diastereoselection Induced by Chiral Silicon in the Addition of Grignard Reagents to Acylsilanes.;ChemInform;2010-08-21
5. Chiral cyclotrisiloxanes;Dalton Transactions;2010
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