Tetrahedron

A new asymmetric synthetic route to substituted piperidines

MS Reddy, M Narender, KR Rao

Index: Reddy, M. Somi; Narender; Rao, K. Rama Tetrahedron, 2007 , vol. 63, # 2 p. 331 - 336

Full Text: HTML

Citation Number: 26

Abstract

An asymmetric synthesis of substituted piperidines has been described. β-Cyclodextrin-or oxazaborolidine-catalyzed asymmetric reduction of α-azido aryl ketones to the corresponding alcohols has been employed as the key step along with ring closing metathesis and selective dihydroxylation.

~10%

Cis-1, 4-bis (triphenylphosphonium)-2-butene Peroxodisulfate...

[Badri, Rashid; Gorjizadeh, Maryam Synthetic Communications, 2012 , vol. 42, # 14 p. 2058 - 2066]

A Novel and Efficient Method for the Synthesis of. ALPHA.-Az...

[Yadav; Subba Reddy; Srinivas Chemistry Letters, 2004 , vol. 33, # 7 p. 882 - 883]

Iodobenzene??catalyzed synthesis of α??azidoketones and α??t...

[Chang, Ya-Li; Chung, Chi-Lin; Wu, Fang-Wen; Wang, Huey-Min; Hou, Rei-Sheu; Kang, Iou-Jiun; Chen, Ling-Ching Journal of the Chinese Chemical Society, 2010 , vol. 57, # 2 p. 149 - 152]

A fast procedure for the preparation of vicinal azidoalcohol...

[Souza Brenelli, Eugenia Cristina; Brenelli, Jose Afranio; Laranjeira Pinto, Raquel Cristina Tetrahedron Letters, 2005 , vol. 46, # 27 p. 4531 - 4533]