Enantioselective Total Synthesis and Determination of the Absolute Configuration of the 4,6,8,10,16,18-Hexamethyldocosane fromAntitrogus parvulus

2005 ◽  
Vol 117 (33) ◽  
pp. 5401-5403 ◽  
Author(s):  
Christian Herber ◽  
Bernhard Breit
ChemInform ◽  
2010 ◽  
Vol 33 (24) ◽  
pp. no-no
Author(s):  
Robert K. Boeckman Jr. ◽  
Maria del Rosario Rico Ferreira ◽  
Lorna H. Mitchell ◽  
Pengcheng Shao

2002 ◽  
Vol 124 (2) ◽  
pp. 190-191 ◽  
Author(s):  
Robert K. Boeckman, ◽  
Maria del Rosario Rico Ferreira ◽  
Lorna H. Mitchell ◽  
Pengcheng Shao

2021 ◽  
Vol 23 (4) ◽  
pp. 1321-1326
Author(s):  
Hongjun Jang ◽  
Soo Yeon Kwak ◽  
Dongjoo Lee ◽  
Juan V. Alegre-Requena ◽  
Hyoungsu Kim ◽  
...  

2001 ◽  
Vol 42 (36) ◽  
pp. 6307-6309 ◽  
Author(s):  
Yoshiki Morimoto ◽  
Toshiyuki Iwai ◽  
Takamasa Kinoshita

1986 ◽  
Vol 51 (8) ◽  
pp. 1731-1742 ◽  
Author(s):  
Josef Hájíček ◽  
Jan Trojánek

A synthesis of (±)-strempeliopine (II) is described, the key step of which is the stereoselective reductive rearrangement of 18-methylene-1,2-dehydroaspidospermidine (XI). The absolute configuration of the natural (-)-base II was determined as (2S, 7R, 20R, 21R) on the basis of its synthesis from (+)-18-methylenevincadifformine (XVII) the configuration of which was derived from a comparison of circular dichroism properties of bases with a β-anilinoacrylate chromophore. The biogenesis of the alkaloids of the schizozygane type is discussed.


ChemInform ◽  
2003 ◽  
Vol 34 (7) ◽  
Author(s):  
Lia Dewi Juliawaty ◽  
Yoshimi Watanabe ◽  
Mariko Kitajima ◽  
Sjamsul Arifin Achmad ◽  
Hiromitsu Takayama ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document