Natural Product Synthesis Featuring Intramolecular Diels-Alder Approaches - Total Syntheses of Tubelactomicins and Spiculoic Acid A

2009 ◽  
Vol 2009 (26) ◽  
pp. 4381-4394 ◽  
Author(s):  
Kin-ichi Tadano
2014 ◽  
Vol 31 (4) ◽  
pp. 533-549 ◽  
Author(s):  
Xu-Wen Li ◽  
Bastien Nay

Important biomimetic steps in natural product synthesis have been promoted by transition metals, as exemplified by this beautiful ruthenium-catalyzed rearrangement of an endoperoxide into elysiapyrone A. Such reactions are supposed to occur during the biosynthesis, yet under different catalysis conditions.


ChemInform ◽  
2003 ◽  
Vol 34 (35) ◽  
Author(s):  
Lars Ole Haustedt ◽  
Ingo V. Hartung ◽  
H. M. R. Hoffmann

2021 ◽  
Vol 16 (10) ◽  
pp. 1934578X2110498
Author(s):  
Hisahiro Hagiwara

Recent advances in the total syntheses of cyclic natural products and related compounds from 2005 to 2021, which employ domino Michael reactions as key steps, have been reviewed, focusing mainly on the domino Michael reactions catalyzed by organocatalysts.


2003 ◽  
Vol 42 (24) ◽  
pp. 2711-2716 ◽  
Author(s):  
Lars Ole Haustedt ◽  
Ingo V. Hartung ◽  
H. M. R. Hoffmann

2005 ◽  
Vol 105 (12) ◽  
pp. 4779-4807 ◽  
Author(s):  
Ken-ichi Takao ◽  
Ryosuke Munakata ◽  
Kin-ichi Tadano

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