The double addition reaction of alkoxymethyl nucleophiles to esters to generate novel polyoxygenated species
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. 4,4′-Di-tert-butylbiphenyl-catalysed lithiation of chloromethyl ethyl ether: A barbier-type new and easy alternative to ethyl lithiomethyl ether
2. Total Synthesis of (+)-Benzastatin E via Diastereoselective Grignard Addition to 2-Acylindoline
3. A new approach for the asymmetric syntheses of 2-epi-deoxoprosopinine and azasugar derivatives
4. Asymmetric Synthesis of (+)-Deoxoprosopinine
5. Convenient One-pot Synthesis of Primary α-Alkoxystannanes
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Synthesis and SAR of geminal substitutions at the C5′ carbosugar position of pyrimidine-derived HCV inhibitors;Bioorganic & Medicinal Chemistry Letters;2012-11
2. A Concise Approach for the Total Synthesis of Pseudolaric Acid A;Organic Letters;2011-04-27
3. ChemInform Abstract: The Double Addition Reaction of Alkoxymethyl Nucleophiles to Esters to Generate Novel Polyoxygenated Species.;ChemInform;2010-11-04
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