The reaction of thioimides with phosphorus ylides
…, JF O'Connell, H Rapoport
Index: Bishop, John E.; O'Connell, John F.; Rapoport, Henry Journal of Organic Chemistry, 1991 , vol. 56, # 17 p. 5079 - 5091
Full Text: HTML
Citation Number: 60
Abstract
The reaction of a series of thioimides with phosphorus ylides, in a manner analogous to the Wittig reaction, has been examined. The resulting reaction products represent potentially valuable intermediates in tetrapyrrole pigment syntheais. In addition to the desired thio- Wittig-type coupling reaction, the presence of two competing reaction pathways, Salkylation and ondation/reduction, has been obeerved with certain substrates. These empirical ...
Related Articles:
A catalytic method for α-glycol cleavage
[Barton, Derek H. R.; Motherwell, William B.; Stobie, Alan Journal of the Chemical Society, Chemical Communications, 1981 , # 23 p. 1232 - 1233]
[Lawson, Edward C.; Santulli, Rosemary J.; Dyatkin, Alexey B.; Ballentine, Scott A.; Abraham, William M.; Rudman, Sandra; Page, Clive P.; de Garavilla, Lawrence; Damiano, Bruce P.; Kinney, William A.; Maryanoff, Bruce E. Bioorganic and Medicinal Chemistry, 2006 , vol. 14, # 12 p. 4208 - 4216]
Simple syntheses of diethyl oxomalonate and alkyl glyoxylates
[Jung, Michael E.; Shishido, Kozo; Davis, Leonard H. Journal of Organic Chemistry, 1982 , vol. 47, # 5 p. 891 - 892]