A New Quinolizidine Alkaloid from Oxytropis ochrocephala

2017 ◽  
Vol 53 (2) ◽  
pp. 322-324 ◽  
Author(s):  
Cheng-Jian Tan ◽  
Li-Na Liu ◽  
Bao-Yu Zhao
Keyword(s):  
Quinolizidine Alkaloid

scholarly journals Responses in rainbow trout (Oncorhynchus mykiss) to increasing dietary doses of lupinine, the main quinolizidine alkaloid found in yellow lupins (Lupinus luteus)

Aquaculture ◽  
2011 ◽  
Vol 318 (1-2) ◽  
pp. 122-127 ◽  
Author(s):  
Edison Serrano ◽  
Trond Storebakken ◽  
Michael Penn ◽  
Margareth Øverland ◽  
Jon Øvrum Hansen ◽  
...  
Keyword(s):  
Rainbow Trout ◽  
Oncorhynchus Mykiss ◽  
Lupinus Luteus ◽  
Quinolizidine Alkaloid ◽  
Rainbow Trout Oncorhynchus Mykiss

Cytisine-12-carboxy-ethylester, a quinolizidine alkaloid from Laburnum watereri and its occurrence in the leguminosae

1990 ◽  
Vol 29 (11) ◽  
pp. 3553-3554 ◽  
Author(s):  
Roland Greinwald ◽  
Peter Bachmann ◽  
Ludger Witte ◽  
Franz-Christian Czygan
Keyword(s):  
Quinolizidine Alkaloid

scholarly journals Quinolizidine Alkaloid Profiles of Two Taxa of Teline maderensis

2003 ◽  
Vol 58 (11-12) ◽  
pp. 776-778 ◽  
Author(s):  
Alice Martins ◽  
Michael Wink ◽  
Andreas Tei ◽  
Amélia P. Rauter
Keyword(s):  
The Other ◽  
Minor Constituent ◽  
Alkaloid Composition ◽  
Quinolizidine Alkaloid ◽  
Aerial Parts ◽  
Capillary Glc ◽  
A Minor ◽  
Alkaloid Profiles

Abstract The alkaloid composition of the aerial parts of two taxa of Teline maderensis was studied by capillary GLC and GLC-MS. N-Methylcytisine was the major alkaloid found in both plants. Contents of cytisine and lupanine were higher in T. maderensis var. paivae while anagyrine content was more pronounced in T. maderensis var. maderensis. The alkaloids dehydrocytisine, N-acetylcytisine and epibaptifoline appeared only in T. maderensis var. maderensis and N-formylcytisine was identified as a minor constituent in T. maderensis var. paivae, and detected only in trace amounts in the other variety of the plant.

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.

Sign in / Sign up

Export Citation Format

Share Document