A TMM Cycloaddition Strategy to the Bicyclo[6.3.0]undecyl Ring System. A Total Synthesis of 11-Hydroxyjasionone

1994 ◽  
Vol 59 (25) ◽  
pp. 7568-7569 ◽  
Author(s):  
Barry M. Trost ◽  
Jon R. Parquette
Keyword(s):  
ChemInform ◽  
2010 ◽  
Vol 28 (8) ◽  
pp. no-no
Author(s):  
M. E. KOPACH ◽  
A. H. FRAY ◽  
A. I. MEYERS
Keyword(s):  

1996 ◽  
Vol 118 (41) ◽  
pp. 9876-9883 ◽  
Author(s):  
Michael E. Kopach ◽  
Andrew H. Fray ◽  
A. I. Meyers
Keyword(s):  

Synlett ◽  
2020 ◽  
Author(s):  
Debendra K. Mohapatra ◽  
Shivalal Banoth ◽  
Utkal Mani Choudhury ◽  
Kanakaraju Marumudi ◽  
Ajit C. Kunwar

AbstractA concise and convergent stereoselective synthesis of curvulone B is described. The synthesis utilized a tandem isomerization followed by C–O and C–C bond-forming reactions following Mukaiyama-type aldol conditions for the construction of the trans-2,6-disubstituted dihydropyran ring system as the key steps. Other important features of this synthesis are a cross-metathesis, epimerization, and Friedel–Crafts acylation.


1975 ◽  
Vol 6 (52) ◽  
pp. no-no
Author(s):  
S. BARCZA ◽  
C. W. HOFFMAN
Keyword(s):  

2021 ◽  
Author(s):  
Yuxiang Zhao ◽  
Yanren Zhu ◽  
Guolan Ma ◽  
Qi Wei ◽  
Shaoxiong Yang ◽  
...  

A reasonable synthesis design by strategically integrating functional group manipulation into the ring system construction resulted in a short, enantioselective, gram-scale total synthesis of (−)-zephyranthine.


Sign in / Sign up

Export Citation Format

Share Document