On 1,4-diastereoselectivity in the chiral allylsilane addition to chiral α-substituted aldehydes
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Stereochemical Control in Organic Synthesis Using Silicon-Containing Compounds
2. Versatile roles of Lewis acids in the reactions of allylic tin compounds
3. A Stereochemical Model for Merged 1,2- and 1,3-Asymmetric Induction in Diastereoselective Mukaiyama Aldol Addition Reactions and Related Processes
4. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones
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1. 2.02 Allylsilanes, Allylstannanes, and Related Compounds;Comprehensive Organic Synthesis II;2014
2. Relative Stereochemical Determination and Synthesis of the C17–C25 δ-Lactone Fragment of Hemicalide;The Journal of Organic Chemistry;2013-01-23
3. Synthesis of the Macrolactone of Migrastatin and Analogues with Potent Cell-Migration Inhibitory Activity;European Journal of Organic Chemistry;2010-10-28
4. ChemInform Abstract: 1,4-Diastereoselectivity in the Chiral Allylsilane Addition to Chiral α-Substituted Aldehydes.;ChemInform;2010-06-19
5. Curiosidades sobre a reação aldólica utilizada como etapa chave na síntese Brasileira dos ácidos pterídicos A e B;Química Nova;2010
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