Stereoselective synthesis of the C-11 to C-19 segment of macrolactin 3 via a center inversion followed by Oxa-Michael addition approach

2017 ◽  
Vol 36 (2-3) ◽  
pp. 100-110
Author(s):  
Prashanth Thodupunuri ◽  
Marumamula Hanumaiah ◽  
Shobanbabu Bommagani ◽  
Gangavaram V. M. Sharma
Keyword(s):  
Michael Addition ◽  
Stereoselective Synthesis

ChemInform Abstract: Stereoselective Synthesis of cis-Decalins via Diels-Alder and Double Michael Addition of Substituted Nazarov Reagents.

ChemInform ◽  
2010 ◽  
Vol 24 (5) ◽  
pp. no-no
Author(s):  
J.-F. LAVALLEE ◽  
C. SPINO ◽  
R. RUEL ◽  
K. T. HOGAN ◽  
P. DESLONGCHAMPS
Keyword(s):  
Michael Addition ◽  
Stereoselective Synthesis ◽  
Diels Alder

Stereoselective synthesis of 2,3,4-highly substituted oxetanes by intramolecular C–C bond forming Michael addition

2016 ◽  
Vol 52 (81) ◽  
pp. 12108-12111 ◽  
Author(s):  
Guo-Ming Ho ◽  
Yu-Jang Li
Keyword(s):  
Michael Addition ◽  
Stereoselective Synthesis ◽  
Unsaturated Ester ◽  
Bond Forming

A wide variety of 2,3,3,4-tetrasubstituted oxetanes and 3-α,β-unsaturated ester substituted oxetanes were synthesized starting from vinylogous urethane derivatives.

Unique Michael Addition-Initiated Domino Reaction for the Stereoselective Synthesis of Functionalized Macrolactones from α-Nitroketones in Water†

2005 ◽  
Vol 7 (11) ◽  
pp. 2197-2200 ◽  
Author(s):  
Giorgio Giorgi ◽  
Sonia Miranda ◽  
Pilar López-Alvarado ◽  
Carmen Avendaño ◽  
Jean Rodriguez ◽  
...  
Keyword(s):  
Michael Addition ◽  
Stereoselective Synthesis ◽  
Domino Reaction
Sign in / Sign up

Export Citation Format

Share Document