Total synthesis of nafuredin B

2020 ◽  
Vol 18 (12) ◽  
pp. 2346-2359
Author(s):  
Gour Hari Mandal ◽  
Dhiman Saha ◽  
Rajib Kumar Goswami

Asymmetric total synthesis of nafuredin B has been achieved for the first time following a convergent approach.

Author(s):  
Hongyuan Zhang ◽  
Haibing He ◽  
Shuanhu Gao

The asymmetric synthesis of cephanolide B, a complex C18 Cephalotaxus dinorditerpenoid, is presented for the first time.


ChemInform ◽  
2010 ◽  
Vol 33 (52) ◽  
pp. no-no
Author(s):  
Sakae Aoyagi ◽  
Shintaro Hirashima ◽  
Kosuke Saito ◽  
Chihiro Kibayashi

2002 ◽  
Vol 67 (16) ◽  
pp. 5517-5526 ◽  
Author(s):  
Sakae Aoyagi ◽  
Shintaro Hirashima ◽  
Kosuke Saito ◽  
Chihiro Kibayashi

2016 ◽  
Vol 14 (45) ◽  
pp. 10581-10584 ◽  
Author(s):  
Xuan Wang ◽  
Wang-Bin Sun ◽  
Jian-Ping Zou ◽  
Guo-Qiang Lin ◽  
Bing-Feng Sun

The asymmetric total syntheses of hedyosumin E aglycon, 7,10-epoxyhedyosminolide and ent-zedolactone A were realized, with the first two being achieved for the first time.


2020 ◽  
Vol 7 (1) ◽  
pp. 109-112
Author(s):  
Yang Ji ◽  
Zhengyuan Xin ◽  
Yingbo Shi ◽  
Haibing He ◽  
Shuanhu Gao

The asymmetric total synthesis of (+)-nodulisporiviridin E was achieved in 16 steps. This convergent approach provides an advanced Michael acceptor, which might facilitate the preparation of various analogues and derivatives for biological studies.


2018 ◽  
Author(s):  
Yaroslav Boyko ◽  
Christopher Huck ◽  
David Sarlah

<div>The first total synthesis of rhabdastrellic acid A, a highly cytotoxic isomalabaricane triterpenoid, has been accomplished in a linear sequence of 14 steps from commercial geranylacetone. The prominently strained <i>trans-syn-trans</i>-perhydrobenz[<i>e</i>]indene core characteristic of the isomalabaricanes is efficiently accessed in a selective manner for the first time through a rapid, complexity-generating sequence incorporating a reductive radical polyene cyclization, an unprecedented oxidative Rautenstrauch cycloisomerization, and umpolung 𝛼-substitution of a <i>p</i>-toluenesulfonylhydrazone with in situ reductive transposition. A late-stage cross-coupling in concert with a modular approach to polyunsaturated side chains renders this a general strategy for the synthesis of numerous family members of these synthetically challenging and hitherto inaccessible marine triterpenoids.</div>


1978 ◽  
Vol 9 (12) ◽  
Author(s):  
W. S. JOHNSON ◽  
R. S. BRINKMEYER ◽  
V. M. KAPOOR ◽  
T. M. YARNELL

Author(s):  
Zhengyuan Xin ◽  
Hui Wang ◽  
Haibing He ◽  
Xiaoli Zhao ◽  
Shuanhu Gao

ACS Omega ◽  
2021 ◽  
Vol 6 (12) ◽  
pp. 8239-8245
Author(s):  
Gang Wu ◽  
Ting Wang ◽  
Zhongke Jiang ◽  
Shaowei Liu ◽  
Chenghang Sun

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