The conjugate addition of enantiomerically pure lithium amides as chiral ammonia equivalents part II: 2005−2011
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference153 articles.
1. The conjugate addition of enantiomerically pure lithium amides as homochiral ammonia equivalents: scope, limitations and synthetic applications
2. Asymmetric synthesis of R-β-amino butanoic acid and S-β-tyrosine: Homochiral lithium amide equivalents for Michael additions to α,β-unsaturated esters.
3. Origins of the high stereoselectivity in the conjugate addition of lithium(α-methylbenzyl)benzylamide to t-butyl cinnamate
4. Ring Closing Metathesis for the Asymmetric Synthesis of (S)-Homopipecolic Acid, (S)-Homoproline and (S)-Coniine
5. Total asymmetric synthesis of sperabillins B and DElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b3/b305740b/
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