Transition metal promoted intramolecular cyclizations of α,α-dichloro esters and acids

Thomas K. Hayes; Alan J. Freyer; M. Parvez; Steven M. Weinreb

Transition metal promoted intramolecular cyclizations of α,α-dichloro esters and acids

Thomas K. Hayes, Alan J. Freyer, M. Parvez, Steven M. Weinreb

Chemistry

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

38 Scopus citations

Abstract

Carbocyclic α,γ-dichloro esters or annulated α-chloro γ-lactones can be selectively synthesized via a radical process starting from olefinic α,α-dichloro esters and acids by appropriate choice of transition-metal catalyst and substrate.

Original language	English (US)
Pages (from-to)	5501-5503
Number of pages	3
Journal	Journal of Organic Chemistry
Volume	51
Issue number	26
State	Published - 1986

All Science Journal Classification (ASJC) codes

Organic Chemistry

Cite this

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title = "Transition metal promoted intramolecular cyclizations of α,α-dichloro esters and acids",

abstract = "Carbocyclic α,γ-dichloro esters or annulated α-chloro γ-lactones can be selectively synthesized via a radical process starting from olefinic α,α-dichloro esters and acids by appropriate choice of transition-metal catalyst and substrate.",

author = "Hayes, {Thomas K.} and Freyer, {Alan J.} and M. Parvez and Weinreb, {Steven M.}",

year = "1986",

language = "English (US)",

volume = "51",

pages = "5501--5503",

journal = "Journal of Organic Chemistry",

issn = "0022-3263",

publisher = "American Chemical Society",

number = "26",

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TY - JOUR

T1 - Transition metal promoted intramolecular cyclizations of α,α-dichloro esters and acids

AU - Hayes, Thomas K.

AU - Freyer, Alan J.

AU - Parvez, M.

AU - Weinreb, Steven M.

PY - 1986

Y1 - 1986

N2 - Carbocyclic α,γ-dichloro esters or annulated α-chloro γ-lactones can be selectively synthesized via a radical process starting from olefinic α,α-dichloro esters and acids by appropriate choice of transition-metal catalyst and substrate.

AB - Carbocyclic α,γ-dichloro esters or annulated α-chloro γ-lactones can be selectively synthesized via a radical process starting from olefinic α,α-dichloro esters and acids by appropriate choice of transition-metal catalyst and substrate.

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M3 - Article

AN - SCOPUS:33845375895

SN - 0022-3263

VL - 51

SP - 5501

EP - 5503

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 26

ER -

Transition metal promoted intramolecular cyclizations of α,α-dichloro esters and acids

Abstract

All Science Journal Classification (ASJC) codes

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