New synthesis of 3-aryl-Nn-propyl-piperidines
MY Chang, ST Chen, NC Chang
Index: Chang, Meng-Yang; Chen, Shui-Tein; Chang, Nein-Chen Tetrahedron, 2002 , vol. 58, # 18 p. 3623 - 3628
Full Text: HTML
Citation Number: 27
Abstract
The synthesis of 3-aryl-Nn-propyl-piperidines is described in six steps starting from α- sulfonyl acetamide via the formal [3+ 3] cycloaddition reaction of the latter into glutarimide. The pathway involves an efficient cycloaddition and regioselective reduction, and yields useful building blocks for heterocyclic chemistry.
Related Articles:
[Hacksell, Uli; Arvidsson, Lars-Erik; Svensson, Uno; Nilsson, J. Lars G. Journal of Medicinal Chemistry, 1981 , vol. 24, # 12 p. 1475 - 1482]
[Hacksell, Uli; Arvidsson, Lars-Erik; Svensson, Uno; Nilsson, J. Lars G. Journal of Medicinal Chemistry, 1981 , vol. 24, # 12 p. 1475 - 1482]
[Hacksell, Uli; Arvidsson, Lars-Erik; Svensson, Uno; Nilsson, J. Lars G. Journal of Medicinal Chemistry, 1981 , vol. 24, # 12 p. 1475 - 1482]
[Hacksell, Uli; Arvidsson, Lars-Erik; Svensson, Uno; Nilsson, J. Lars G. Journal of Medicinal Chemistry, 1981 , vol. 24, # 12 p. 1475 - 1482]