Total Synthesis of Incarvilleatone and Incarviditone: Insight into Their Biosynthetic Pathways and Structure Determination

2012 ◽  
Vol 14 (18) ◽  
pp. 4878-4881 ◽  
Author(s):  
Kun Zhao ◽  
Gui-Juan Cheng ◽  
Hongzhi Yang ◽  
Hai Shang ◽  
Xinhao Zhang ◽  
...  
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Gentoku Takasao ◽  
Toru Wada ◽  
Ashutosh Thakur ◽  
Patchanee Chammingkwan ◽  
Minoru Terano ◽  
...  

2020 ◽  
Vol 60 (1) ◽  
pp. 446-454 ◽  
Author(s):  
Saskia Schulthoff ◽  
James Y. Hamilton ◽  
Marc Heinrich ◽  
Yonghoon Kwon ◽  
Conny Wirtz ◽  
...  

ChemInform ◽  
2005 ◽  
Vol 36 (19) ◽  
Author(s):  
Ted C. Judd ◽  
Alexander Bischoff ◽  
Yoshito Kishi ◽  
Sarojini Adusumilli ◽  
Pamela L.C. Small

1984 ◽  
Vol 49 (4) ◽  
pp. 735-736 ◽  
Author(s):  
Ting Ting Jong ◽  
Paul G. Willard ◽  
Joseph P. Porwoll

1982 ◽  
Vol 60 (4) ◽  
pp. 509-513 ◽  
Author(s):  
John W. ApSimon ◽  
Rick P. Sequin ◽  
Carol P. Huber

The title compound was made following a projected synthetic route to pentacyclic triterpenes. The key step in the route is the alkylative trapping of the enolate derived from the enol trimethylsilyl ether 8. The stereochemical consequence of this reaction is confirmed by a single crystal X-ray structure determination on 4, which although of no further utility in the projected synthesis, nevertheless served as a useful template for this determination. In this way, ongoing work in a parallel series of compounds rests on a firm stereochemical footing.


2004 ◽  
Vol 6 (26) ◽  
pp. 4901-4904 ◽  
Author(s):  
Ted C. Judd ◽  
Alexander Bischoff ◽  
Yoshito Kishi ◽  
Sarojini Adusumilli ◽  
Pamela L. C. Small

ChemInform ◽  
2004 ◽  
Vol 35 (50) ◽  
Author(s):  
Noriyoshi Arai ◽  
Noriko Chikaraishi ◽  
Satoshi Omura ◽  
Isao Kuwajima

2019 ◽  
Vol 84 (9) ◽  
pp. 4971-4991 ◽  
Author(s):  
Erin D. Shepherd ◽  
Bryony S. Dyson ◽  
William E. Hak ◽  
Quynh Nhu N. Nguyen ◽  
Miseon Lee ◽  
...  

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