scholarly journals Enantioselective Total Synthesis of Bioactive Natural Product (+)-Sch 642305: A Structurally Novel Inhibitor of Bacterial DNA Primase and HIV-1 Tat Transactivation.

ChemInform ◽  
2005 ◽  
Vol 36 (50) ◽  
Author(s):  
Goverdhan Mehta ◽  
Harish M. Shinde
Keyword(s):  
Total Synthesis ◽  
Natural Product ◽  
Bacterial Dna ◽  
Dna Primase ◽  
Enantioselective Total Synthesis ◽  
Bioactive Natural Product ◽  
Hiv 1

ChemInform Abstract: The Enantioselective Total Synthesis of the Antitumor Macrolide Natural Product Rhizoxin D.

ChemInform ◽  
2010 ◽  
Vol 30 (32) ◽  
pp. no-no
Author(s):  
Jennifer A. Lafontaine ◽  
David P. Provencal ◽  
Cristina Gardelli ◽  
James W. Leahy
Keyword(s):  
Total Synthesis ◽  
Natural Product ◽  
Enantioselective Total Synthesis ◽  
Rhizoxin D

Enantioselective total synthesis of periconiasin A

2018 ◽  
Vol 5 (5) ◽  
pp. 838-840 ◽  
Author(s):  
Zhixiong Zeng ◽  
Cheng Chen ◽  
Yandong Zhang
Keyword(s):  
Total Synthesis ◽  
Natural Product ◽  
Enantioselective Total Synthesis

A concise, enantioselective total synthesis of periconiasin A, a hybrid natural product, has been achieved.

ChemInform Abstract: First Enantioselective Total Synthesis of (-)-Dysibetaine CPa and Absolute Configurations of Natural Product

ChemInform ◽  
2014 ◽  
Vol 45 (9) ◽  
pp. no-no
Author(s):  
Michihiro Sakai ◽  
Yuichi Ishikawa ◽  
Satoshi Takamizawa ◽  
Masato Oikawa
Keyword(s):  
Total Synthesis ◽  
Natural Product ◽  
Enantioselective Total Synthesis

Enantioselective total synthesis of (S)-nakinadine B

RSC Advances ◽  
2016 ◽  
Vol 6 (31) ◽  
pp. 25913-25917 ◽  
Author(s):  
Yuvraj Garg ◽  
Satyendra Kumar Pandey
Keyword(s):  
Total Synthesis ◽  
Natural Product ◽  
Michael Addition ◽  
Marine Natural Product ◽  
Enantioselective Total Synthesis ◽  
Novel Approach ◽  
Key Steps

A novel approach for the synthesis of (S)-nakinadine B, a marine natural product is described. The synthesis utilizes the optimized combination of organocatalyzed Michael addition and aminoxylation reactions as key steps.

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