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

doi:10.1016/S0040-4039(00)97677-9

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

Chemistry and Biochemistry

Research output: Contribution to journal › Article › peer-review

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 language	English (US)
Pages (from-to)	4565-4568
Number of pages	4
Journal	Tetrahedron Letters
Volume	31
Issue number	32
DOIs	https://doi.org/10.1016/S0040-4039(00)97677-9
State	Published - 1990

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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

In: Tetrahedron Letters, Vol. 31, No. 32, 1990, p. 4565-4568.

Research output: Contribution to journal › Article › peer-review

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

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