Tetrahedron letters

A convenient and efficient three-step synthesis of α-chloro keto acids

KB Chai, P Sampson

Index: Chai, Ki-Byung; Sampson, Paul Tetrahedron Letters, 1992 , vol. 33, # 5 p. 585 - 588

Full Text: HTML

Citation Number: 9

Abstract

Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Efficient three-step syntheses of α-chloro keto acids 1a-c from ω-alkenoic acids 2 and ω-alkenyl alcohols 3 are described, proceeding via epoxidation/chloride-mediated epoxide ring opening/Jones oxidation protocols. ... Efficient three-step (epoxidation/regioselective ...

Related Articles:

A new and efficient approach to macrocyclic keto lactones

[Karim, Mohammad R.; Sampson, Paul Journal of Organic Chemistry, 1990 , vol. 55, # 2 p. 598 - 605]

Transannular aldol condensations within macrocyclic lactones: A novel approach to 8-membered carbocyclic rings.

[Karim, Mohammad R.; Sampson, Paul Tetrahedron Letters, 1988 , vol. 29, # 52 p. 6897 - 6900]

Alkylation of brain corticosteroid acetyltransferase by 17-hydroxyprogesterone 17-(9-oxo-10-chlorodecanoate) and related compounds

[Purdy,R.H. et al. Steroids, 1973 , vol. 22, p. 139 - 150]

Alkylation of brain corticosteroid acetyltransferase by 17-hydroxyprogesterone 17-(9-oxo-10-chlorodecanoate) and related compounds

[Purdy,R.H. et al. Steroids, 1973 , vol. 22, p. 139 - 150]

Alkylation of brain corticosteroid acetyltransferase by 17-hydroxyprogesterone 17-(9-oxo-10-chlorodecanoate) and related compounds

[Purdy,R.H. et al. Steroids, 1973 , vol. 22, p. 139 - 150]

More Articles...