Formal Total Synthesis of Diazonamide A by Indole Oxidative Rearrangement

2016 ◽  
Vol 22 (31) ◽  
pp. 10867-10876 ◽  
Author(s):  
Nadège David ◽  
Raffaele Pasceri ◽  
Russell R. A. Kitson ◽  
Alexandre Pradal ◽  
Christopher J. Moody
Keyword(s):  
Total Synthesis ◽  
Diazonamide A ◽  
Oxidative Rearrangement

scholarly journals Back Cover: Formal Total Synthesis of Diazonamide A by Indole Oxidative Rearrangement (Chem. Eur. J. 31/2016)

2016 ◽  
Vol 22 (31) ◽  
pp. 11088-11088
Author(s):  
Nadège David ◽  
Raffaele Pasceri ◽  
Russell R. A. Kitson ◽  
Alexandre Pradal ◽  
Christopher J. Moody
Keyword(s):  
Total Synthesis ◽  
Diazonamide A ◽  
Back Cover ◽  
Oxidative Rearrangement

scholarly journals Total synthesis of diazonamide A

2011 ◽  
Vol 2 (2) ◽  
pp. 308-311 ◽  
Author(s):  
Robert R. Knowles ◽  
Joseph Carpenter ◽  
Simon B. Blakey ◽  
Akio Kayano ◽  
Ian K. Mangion ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Diazonamide A

Bioinspired Total Synthesis of the Dimeric Indole Alkaloid (+)-Haplophytine by Direct Coupling and Late-Stage Oxidative Rearrangement

2016 ◽  
Vol 128 (48) ◽  
pp. 15381-15385
Author(s):  
Hitoshi Satoh ◽  
Ken-ichi Ojima ◽  
Hirofumi Ueda ◽  
Hidetoshi Tokuyama
Keyword(s):  
Total Synthesis ◽  
Late Stage ◽  
Indole Alkaloid ◽  
Direct Coupling ◽  
Oxidative Rearrangement

Chemistry and Biology of Diazonamide A:  Second Total Synthesis and Biological Investigations

2004 ◽  
Vol 126 (40) ◽  
pp. 12897-12906 ◽  
Author(s):  
K. C. Nicolaou ◽  
Junliang Hao ◽  
Mali V. Reddy ◽  
Paraselli Bheema Rao ◽  
Gerasimos Rassias ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Diazonamide A

Synthesis of Carbocyclic Nucleosides (+)-Neplanocin A, (+)-Aristeromycin and 4'-epi-(+)-Aristeromycin from D-Fructose

2019 ◽  
Vol 16 (9) ◽  
pp. 750-758
Author(s):  
Perali R. Sridhar ◽  
Vennam D.K. Reddy ◽  
Mandava Suresh ◽  
Nadiveedhi M. Reddy ◽  
K. Shiva Kumar
Keyword(s):  
Total Synthesis ◽  
Allylic Alcohol ◽  
Starting Material ◽  
Carbocyclic Nucleosides ◽  
Ring Closing Metathesis ◽  
Neplanocin A ◽  
Oxidative Rearrangement ◽  
Key Steps

D-Fructose is used as the chiral pool starting material for the stereoselective total synthesis of (+)-neplanocin A. Zinc mediated fragmentation, ring-closing metathesis and oxidative rearrangement of cyclic tertiary allylic alcohol are used as the key steps in achieving the synthesis of key carbocylic intermediate. Further, stereoselective total synthesis of 4'-epi-(+)-aristeromycin and the conversion of (+)-neplanocin A to a mixture of (+)-aristeromycin and 4'-epi-(+)-aristeromycin are described.

scholarly journals Chemistry and Biology of Diazonamide A:  First Total Synthesis and Confirmation of the True Structure [J. Am. Chem. Soc.2004,126, 12888−12896].

2004 ◽  
Vol 126 (46) ◽  
pp. 15316-15316
Author(s):  
K. C. Nicolaou ◽  
David Y.-K. Chen ◽  
Xianhai Huang ◽  
Taotao Ling ◽  
Marco Bella ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Diazonamide A ◽  
True Structure

A Concise and Flexible Total Synthesis of (−)-Diazonamide A

2003 ◽  
Vol 115 (40) ◽  
pp. 5111-5116 ◽  
Author(s):  
Anthony W. G. Burgett ◽  
Qingyi Li ◽  
Qi Wei ◽  
Patrick G. Harran
Keyword(s):  
Total Synthesis ◽  
Diazonamide A

The Second Total Synthesis of Diazonamide A

2003 ◽  
Vol 42 (15) ◽  
pp. 1753-1758 ◽  
Author(s):  
K. C. Nicolaou ◽  
Paraselli Bheema Rao ◽  
Junliang Hao ◽  
Mali Venkat Reddy ◽  
Gerasimos Rassias ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Diazonamide A
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