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 › peer-review

78 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 (US)
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
State	Published - 1984
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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@article{b357191d62de4451892614cf6060c116,

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

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

author = "Posner, {Gary H.} and Kogan, {Timothy P.} and Martin Hulce",

year = "1984",

doi = "10.1016/S0040-4039(00)99889-7",

language = "English (US)",

volume = "25",

pages = "383--386",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

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T1 - Enantiocontrolled synthesis of quaternary carbon centers. 3,3-Disubstituted cyclopentanones. (+)-α-cuparenone.

AU - Posner, Gary H.

AU - Kogan, Timothy P.

AU - Hulce, Martin

PY - 1984

Y1 - 1984

N2 - Asymmetric synthetic methodology is introduced for preparation of 3,3-disubstituted cyclopentanones, including (+)-α-cuparenone, of high enantiomeric purity.

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

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U2 - 10.1016/S0040-4039(00)99889-7

DO - 10.1016/S0040-4039(00)99889-7

M3 - Article

AN - SCOPUS:0000153005

VL - 25

SP - 383

EP - 386

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 4

ER -

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

Abstract

All Science Journal Classification (ASJC) codes

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