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 & Biochemistry - Sci

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

8 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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title = "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",

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

author = "Mash, \{Eugene A.\} and Kaczynski, \{Michelle A.\} and Dolata, \{Daniel P.\}",

note = "Funding Information: Partial support of this research by the Howard Hughes Medical by the University of Arizona Poundation and the Office of the for Research is gratefully acknowledged.",

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doi = "10.1016/S0040-4039(00)97677-9",

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AU - Mash, Eugene A.

AU - Kaczynski, Michelle A.

AU - Dolata, Daniel P.

N1 - Funding Information: Partial support of this research by the Howard Hughes Medical by the University of Arizona Poundation and the Office of the for Research is gratefully acknowledged.

PY - 1990

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AB - 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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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

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