The Decarboxylative Acylation of α-Substituted Acids
JA King, FH McMillan
Index: King; McMillan Journal of the American Chemical Society, 1955 , vol. 77, p. 2814
Full Text: HTML
Citation Number: 9
Abstract
It has been shown that carboxylic acids having certain electron-withdrawing groups attached to the a-position to the carboxyl group can be made to undergo a decarboxylative acylation reaction in the presence of an acylating agent and a base to give a compound in which the original carboxyl group is replaced by an acyl group. The types of electronwithdrawing groups are varied and there are in all probability at least two major routes by which this ...
Related Articles:
[Saito, Akio; Taniguchi, Akihiro; Kambara, Yui; Hanzawa, Yuji Organic Letters, 2013 , vol. 15, # 11 p. 2672 - 2675]
Mono et difluoration electrochimiques de groupes benzyliques
[Laurent, Eliane; Marquet, Bernard; Tardivel, Robert Tetrahedron, 1989 , vol. 45, # 14 p. 4431 - 4444]
Efficient synthesis of multi-substituted oxazoles under solvent-free microwave irradiation
[Lee, Jong Chan; Choi, Hyun Jung; Lee, Yong Chan Tetrahedron Letters, 2003 , vol. 44, # 1 p. 123 - 125]
[Nagayoshi, Kazuo; Sato, Tadashi Chemistry Letters, 1983 , p. 1355 - 1356]
Copper??Catalyzed Direct Synthesis of Iodoenamides from Ketoximes
[Liang, Hao; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui Chemistry - A European Journal, 2013 , vol. 19, # 30 p. 9789 - 9794]