Diastereofacial selectivity in the 1,3-dipolar cycloaddition of chiral azomethine ylides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Diastereofacial selectivity in azomethine ylide cycloaddition reactions derived from chiral α-cyanoaminosilanes
2. Negron, G.; Chastanet, J.; Roussi, G. personal communication (submitted : J. Org. Chem.)
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. The First Asymmetric 1,3-Dipolar Cycloaddition of 1-Methyl-3-oxidopyridinium and (R)s-p-Tolyl Vinyl Sulfoxide. An Enantioselective Synthesis of (1S)-(−)-2α-Tropanol
5. Asymmetric 1,3-dipolar cycloadditions of azomethine ylides with a chiral electron-deficient olefinic dipolarophile
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