960化工网
Highly enantioselective [4+2] annulation via organocatalytic Mannich-reductive cyclization: one-pot synthesis of functionalized piperidines†
Indresh Kumar,Panduga Ramaraju,Nisar A. Mir,Deepika Singh,Vivek K. Gupta,Rajnikant
Chemical Communications Pub Date : 05/03/2013 00:00:00 , DOI:10.1039/C3CC42431F
Abstract

A new method for one-pot synthesis of 2,3-substituted piperidine from N-PMP aldimine and aqueous glutaraldehyde via formal [4+2] cycloaddition is reported. This reaction involves organocatalytic direct Mannich reaction–reductive cyclization with high yields (up to 90%) and excellent enantioselectivities (up to >99%). The practicability of this method is also shown at a gram scale as well as through the synthesis of functionalized (−)-anabasine.

Graphical abstract: Highly enantioselective [4+2] annulation via organocatalytic Mannich-reductive cyclization: one-pot synthesis of functionalized piperidines
平台客服
平台客服
平台在线客服