Total Syntheses of Vellosimine,N-Methylvellosimine, and 10-Methoxyvellosimine and Formal Synthesis of 16-Epinormacusine B through a [5+2] Cycloaddition

2016 ◽  
Vol 2016 (28) ◽  
pp. 4893-4899 ◽  
Author(s):  
Sebastian Krüger ◽  
Tanja Gaich
ChemInform ◽  
2003 ◽  
Vol 34 (47) ◽  
Author(s):  
Yasuyuki Kita ◽  
Junko Futamura ◽  
Yusuke Ohba ◽  
Yoshinari Sawama ◽  
Jnaneshwara K. Ganesh ◽  
...  

2021 ◽  
Vol 2021 (17) ◽  
pp. 2540-2548
Author(s):  
Thomas Mies ◽  
Calum Patel ◽  
Philip J. Parsons ◽  
Anthony G. M. Barrett

2017 ◽  
Vol 12 (12) ◽  
pp. 1309-1313 ◽  
Author(s):  
Yong-Jian Chen ◽  
Sen-Lin Cai ◽  
Chuan-Chuan Wang ◽  
Jin-Duo Cheng ◽  
Søren Kramer ◽  
...  

Synthesis ◽  
2017 ◽  
Vol 50 (01) ◽  
pp. 17-34 ◽  
Author(s):  
Arun Shaw ◽  
Sama Ajay

Anisomycin shows potent biological activity and it has attracted much attention since its isolation in 1954, with around 13 total syntheses and 20 formal syntheses, and also two reports concerning analogues of anisomycin, reported to date. The present review highlights all of these synthetic approaches (around 35) to the total or formal synthesis of anisomycin along with its isomers and analogues.1 Introduction2 Isolation and Therapeutic Importance3 Total Synthesis of (+)-, (–)-, and (±)-Anisomycins and Their Analogues4 Formal Synthesis of (+)- and (–)-Anisomycins and Their Analogues5 Conclusion


2013 ◽  
Vol 8 (7) ◽  
pp. 1934578X1300800
Author(s):  
Tadashi Katoh

Otteliones A and B isolated from the freshwater plant Ottelia alismoides have attracted significant attention because of their potential as novel anticancer agents. In this review four independent enantioselective total syntheses and one formal synthesis of these natural products are presented with particular focus on their methodology and strategy.


2003 ◽  
Vol 68 (15) ◽  
pp. 5917-5924 ◽  
Author(s):  
Yasuyuki Kita ◽  
Junko Futamura ◽  
Yusuke Ohba ◽  
Yoshinari Sawama ◽  
Jnaneshwara K. Ganesh ◽  
...  

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