scholarly journals Stereoselective synthesis of 2,6-trans-4-oxopiperidines using an acid-mediated 6-endo-trig cyclisation

2018 ◽  
Vol 16 (35) ◽  
pp. 6410-6422 ◽  
Author(s):  
Jonathan D. Bell ◽  
Alexander H. Harkiss ◽  
Christopher R. Wellaway ◽  
Andrew Sutherland
Keyword(s):  
Stereoselective Synthesis ◽  
Quinolizidine Alkaloid

An acid-mediated 6-endo-trig cyclisation has been developed for the synthesis of trans-6-alkyl-2-methyl-4-oxopiperidines and used for the stereoselective preparation of quinolizidine alkaloid, (+)-myrtine and the piperidine alkaloid, (−)-solenopsin A.

Stereoselective Synthesis of Quinolizidine Alkaloids: (–)-Lasubin II

2008 ◽  
Vol 63 (4) ◽  
pp. 425-430 ◽  
Author(s):  
Markus Weymann ◽  
Horst Kunz
Keyword(s):  
Mannich Reaction ◽  
Stereoselective Synthesis ◽  
Pure Form ◽  
Quinolizidine Alkaloids ◽  
Enantiomerically Pure ◽  
Quinolizidine Alkaloid

AbstractBased on a higly diastereoselective Mannich reaction of N-(3,4-dimethoxybenzylidene) 2,3,4,6- tetra-O-pivaloyl-β -D-galactopyranosylamine 3 with the Danishefsky diene the quinolizidine alkaloid lasubin II was synthesized in enantiomerically pure form in six steps.

Stereoselective synthesis of Nuphar quinolizidine alkaloid, (−)-deoxynupharidine

2005 ◽  
Vol 46 (31) ◽  
pp. 5161-5163 ◽  
Author(s):  
Miho Katoh ◽  
Hirotake Mizutani ◽  
Toshio Honda
Keyword(s):  
Stereoselective Synthesis ◽  
Quinolizidine Alkaloid

Stereoselective Synthesis of Nuphar Quinolizidine Alkaloid, (-)-Deoxynupharidine.

ChemInform ◽  
2005 ◽  
Vol 36 (48) ◽  
Author(s):  
Miho Katoh ◽  
Hirotake Mizutani ◽  
Toshio Honda
Keyword(s):  
Stereoselective Synthesis ◽  
Quinolizidine Alkaloid
Sign in / Sign up

Export Citation Format

Share Document