Highly diastereoselective additions of organometallic reagents to 1-O-silylated 3,4-Di-O-benzyl-L-erythrulose derivatives
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference9 articles.
1. Diastereoselective synthesis of enantiomeric tertiary alcohols via nucleophilic additions to protected D- and L-erythrulose derivatives
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1. Reactions of Allylmagnesium Reagents with Carbonyl Compounds and Compounds with C═N Double Bonds: Their Diastereoselectivities Generally Cannot Be Analyzed Using the Felkin–Anh and Chelation-Control Models;Chemical Reviews;2020-01-06
2. Reactions of Allylmagnesium Halides with Carbonyl Compounds: Reactivity, Structure, and Mechanism;Synthesis;2017-06-28
3. Diastereoselective Additions of Allylmetal Reagents to Free and Protected syn-α,β-Dihydroxyketones Enable Efficient Synthetic Routes to Methyl Trioxacarcinoside A;Organic Letters;2012-03-09
4. ChemInform Abstract: Highly Diastereoselective Additions of Organometallic Reagents to 1-O- Silylated 3,4-Di-O-benzyl-L-erythrulose Derivatives.;ChemInform;2010-08-20
5. Theoretical Studies of the Addition of RMgX to Carbonyl Compounds;PATAI'S Chemistry of Functional Groups;2009-12-15
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