High diastereofacial selectivity in the 1,3-dipolar cycloaddition of chiral azomethine ylides
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference17 articles.
1. Diastereofacial selectivity in azomethine ylide cycloaddition reactions derived from chiral α-cyanoaminosilanes
2. Negron, G.; Chastanet, J.; Roussi, G. Personal communication (J. Org. Chem. submitted).
3. An approach to the 3,8-diazabicyclo[3.2.1]octane moiety of naphthyridinomycin and quinocarcin via 1,3-dipolar cycloaddition of photochemically generated azomethine ylides.
4. Development of a chiral stabilised azomethine ylid. A chiral relay system.
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