Enantiocontrolled synthesis of quaternary carbon centers. 3,3-Disubstituted cyclopentanones. (+)-α-cuparenone.

Gary H. Posner; Timothy P. Kogan; Martin Hulce

doi:10.1016/S0040-4039(00)99889-7

Enantiocontrolled synthesis of quaternary carbon centers. 3,3-Disubstituted cyclopentanones. (+)-α-cuparenone.

Gary H. Posner, Timothy P. Kogan, Martin Hulce

Research output: Contribution to journal › Article

77 Scopus citations

Abstract

Asymmetric synthetic methodology is introduced for preparation of 3,3-disubstituted cyclopentanones, including (+)-α-cuparenone, of high enantiomeric purity.

Original language	English
Pages (from-to)	383-386
Number of pages	4
Journal	Tetrahedron Letters
Volume	25
Issue number	4
DOIs	https://doi.org/10.1016/S0040-4039(00)99889-7
Publication status	Published - 1984
Externally published	Yes

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All Science Journal Classification (ASJC) codes

Biochemistry
Organic Chemistry
Drug Discovery

Cite this

Posner, G. H., Kogan, T. P., & Hulce, M. (1984). Enantiocontrolled synthesis of quaternary carbon centers. 3,3-Disubstituted cyclopentanones. (+)-α-cuparenone. Tetrahedron Letters, 25(4), 383-386. https://doi.org/10.1016/S0040-4039(00)99889-7

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abstract = "Asymmetric synthetic methodology is introduced for preparation of 3,3-disubstituted cyclopentanones, including (+)-α-cuparenone, of high enantiomeric purity.",

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Access to Document

10.1016/S0040-4039(00)99889-7