An Iterative Acetylene-Epoxide Coupling Strategy for the Total Synthesis of Aspinolide A

2011 ◽  
Vol 94 (2) ◽  
pp. 224-229 ◽  
Author(s):  
Gowravaram Sabitha ◽  
Teega Rammohan Reddy ◽  
Chitti Srinivas ◽  
Jhillu Singh Yadav
ChemInform ◽  
2009 ◽  
Vol 40 (46) ◽  
Author(s):  
Michael T. Crimmins ◽  
J. Lucas Zuccarello ◽  
Patrick J. McDougall ◽  
J. Michael Ellis

2009 ◽  
Vol 15 (36) ◽  
pp. 9235-9244 ◽  
Author(s):  
Michael T. Crimmins ◽  
J. Lucas Zuccarello ◽  
Patrick J. McDougall ◽  
J. Michael Ellis

2005 ◽  
Vol 46 (32) ◽  
pp. 5393-5397 ◽  
Author(s):  
Yan-Tao He ◽  
Song Xue ◽  
Tai-Shan Hu ◽  
Zhu-Jun Yao

Synthesis ◽  
2020 ◽  
Vol 52 (20) ◽  
pp. 3007-3017
Author(s):  
Kazuhiko Sakaguchi ◽  
Yuto Nishioka ◽  
Naoto Kinashi ◽  
Nao Yukihira ◽  
Tetsuro Shinada ◽  
...  

The stereocontrolled total synthesis of the allene and carbonyl conjugated apocarotenoids, paracentrone and 19-hexanoyloxyparacentrone 3-acetate, was achieved by sequential cross-coupling reactions using boronic acid ester and iodine- or tin-substituted C5 dienes, which were the building blocks for the elongation of the conjugated polyene systems at both terminals.


2015 ◽  
Vol 17 (15) ◽  
pp. 3918-3921 ◽  
Author(s):  
Keita Komine ◽  
Yusuke Nomura ◽  
Jun Ishihara ◽  
Susumi Hatakeyama

2013 ◽  
Vol 19 (31) ◽  
pp. 10132-10137 ◽  
Author(s):  
Yan-Ping Zhu ◽  
Mei-Cai Liu ◽  
Qun Cai ◽  
Feng-Cheng Jia ◽  
An-Xin Wu

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