Reaction of chromium (Fischer) carbenes and sulfilimines
B Alcaide, L Casarrubios, G Dominguez…
Index: Alcaide, Benito; Casarrubios, Luis; Dominguez, Gema; Sierra, Miguel A. Journal of Organic Chemistry, 1993 , vol. 58, # 15 p. 3886 - 3894
Full Text: HTML
Citation Number: 12
Abstract
The photochemical reactions of alkoxychromium (Fischer) carbenes and sulfilimines lead to imidatss in fair to excellent yields. Aromatic, heteroaromatic, and alkylsulfiies, the latter bearing functional groups such as cyano, sulfone, ether, ester, and dioxolane groups, gave the corresponding imidates in good to excellent yield. However, acyl-and sulfonyl- substituted sulfilimines did not react with chromium carbenes, except for sulfilimines ...
Related Articles:
The course of the reaction of azobenzene with chromium carbene complexes
[Hegedus, Louis S.; Lundmark, Bruce R. Journal of the American Chemical Society, 1989 , vol. 111, # 20 p. 9194 - 9198]
[Sleiman, Hanadi F.; Mercer, Suzanne; McElwee-White, Lisa Journal of the American Chemical Society, 1989 , vol. 111, # 20 p. 8007 - 8009]
[Mloston, Grzegorz; Romanski, Jaroslaw; Linden, Anthony; Heimgartner, Heinz Helvetica Chimica Acta, 1995 , vol. 78, # 6 p. 1499 - 1510]
A new approach to N-aryl-and N-(2-heteroaryl) imidates from chromium carbenes and sulfilimines
[Alcaide, Benito; Dominguez, Gema; Plumet, Joaquin; Sierra, Miguel A. Organometallics, 1991 , vol. 10, p. 11 - 12]
[Lee, Jung June; Kim, Jihye; Jun, Young Moo; Lee, Byung Min; Kim, Byeong Hyo Tetrahedron, 2009 , vol. 65, # 43 p. 8821 - 8831]