ChemInform Abstract: TOTAL SYNTHESIS OF NATURAL α-TOCOPHEROL. 3. FORMATION OF THE SIDE CHAIN N WITH (-)-S-2-METHYL-Γ-BUTYROLACTONE AS THE CENTRAL BUILDING BLOCK

1979 ◽  
Vol 10 (22) ◽  
Author(s):  
R. ZELL
2021 ◽  
Author(s):  
Venugopal Rao Challa ◽  
Daniel Kwon ◽  
Matthew Taron ◽  
Hope Fan ◽  
Baldip Kang ◽  
...  

A total synthesis of the marine macrolide biselide A is described that relies on an enantiomerically enriched α-chloroaldehyde as the sole chiral building block.


ChemInform ◽  
2000 ◽  
Vol 31 (49) ◽  
pp. no-no
Author(s):  
Young S. Rho ◽  
Hyun Kyoung Ko ◽  
Wan-Joong Kim ◽  
Dong Jin Yoo ◽  
Heun Soo Kang
Keyword(s):  

2015 ◽  
Vol 73 (4) ◽  
pp. 959-973 ◽  
Author(s):  
Guilherme D. Vilela ◽  
Thaís H. M. Fernandes ◽  
Rafaela Raupp da Rosa ◽  
Stephen M. Kelly ◽  
Stuart P. Kitney ◽  
...  

2012 ◽  
Vol 1 (5) ◽  
pp. 641-645 ◽  
Author(s):  
Jun-Feng Zheng ◽  
Xin Liu ◽  
Xiao-Fang Chen ◽  
Xiang-Kui Ren ◽  
Shuang Yang ◽  
...  

2015 ◽  
Vol 6 (2) ◽  
pp. 1061-1074 ◽  
Author(s):  
Kai Pahnke ◽  
Josef Brandt ◽  
Ganna Gryn'ova ◽  
Peter Lindner ◽  
Ralf Schweins ◽  
...  

Entropic chain effects on dynamic bonding reactions are shown to enable the tuning of reaction equilibria not only by changing the mass of the reactants, but also by merely altering the building block side chain structure and thus the intrinsic stiffness. The findings enable a step change for the design of on-demand bonding systems and reversible ligation chemistry in general.


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