Electrolytic Reductive Coupling. XIII. 1 Intramolecular Reductive Coupling. Electrohydrocyclization2
JD Anderson, MM Baizer…
Index: Anderson,J.D. et al. Journal of Organic Chemistry, 1966 , vol. 31, p. 3890 - 3897
Full Text: HTML
Citation Number: 53
Abstract
Electrolytic reductive coupling has been extended to intramolecular reactions which have been found capable of yielding a wide variety of cyclic compounds. A series of bisactivated olefins, ROOCCH= CH (CRz), CH= CHCOOR, gave high yields of ring compounds by p-to-p coupling when n was 1, 2, 3, and 4; the proposed mechanism of the reaction explained the fact that only acyclic products were formed when n was greater than 4. The reaction was ...
Related Articles:
The preparation of ethyl 18-nonadecenoate by a mixed coupling reaction
[Suhara,Y.; Miyazaki,S. Bulletin of the Chemical Society of Japan, 1970 , vol. 43, p. 3924 - 3925]