Diastereoselective manipulations of conformationally restricted enantiomerically pure bicyclo[m.1.0]alkanes. 1. Nucleophilic additions to the carbonyl carbons of bicyclo[m.1.0]alkan-2-ones

Eugene A. Mash, Michelle A. Kaczynski, Daniel P. Dolata

Research output: Contribution to journalArticle

7 Scopus citations

Abstract

Additions of nucleophiles to the carbonyls of several enantiomerically pure bicyclo[m.1.0]alkan-2-ones were found to be highly diastereoselective.

Original languageEnglish (US)
Pages (from-to)4565-4568
Number of pages4
JournalTetrahedron Letters
Volume31
Issue number32
DOIs
StatePublished - 1990

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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