Biogenetically-modelled total syntheses (−)-nocardicin A and (−)-nocardicin G

1986 ◽  
Vol 27 (33) ◽  
pp. 3819-3822 ◽  
Author(s):  
Craig A Townsend ◽  
Gino M Salituro ◽  
Loan T Nguyen ◽  
Michael J DiNovi
Keyword(s):  
1986 ◽  
Vol 17 (50) ◽  
Author(s):  
C. A. TOWNSEND ◽  
G. M. SALITURO ◽  
L. T. NGUYEN ◽  
M. J. DINOVI
Keyword(s):  

2013 ◽  
Vol 17 (19) ◽  
pp. 2192-2224 ◽  
Author(s):  
Majid Heravi ◽  
Elaheh Hashemi ◽  
Nazanin Ghobadi

2014 ◽  
Vol 11 (6) ◽  
pp. 787-823 ◽  
Author(s):  
Majid Heravi ◽  
Atefe Bakhtiari ◽  
Zeinab Faghihi
Keyword(s):  

2005 ◽  
Vol 70 (10) ◽  
pp. 1696-1708 ◽  
Author(s):  
Magnus Besev ◽  
Christof Brehm ◽  
Alois Fürstner

A concise route to the common polyketide fragment5of crocacin A-D (1-4) is presented which has previously been converted into all members of this fungicidal and cytotoxic family of dipeptidic natural products by various means. Our synthesis features asyn-selective titanium aldol reaction controlled by a valinol-derived auxiliary, a zinc-mediated, palladium-catalyzedanti-selective addition of propargyl mesylate10to the chiral aldehyde9, as well as a comparison of palladium-catalyzed Stille and Suzuki cross-coupling reactions for the formation of the diene moiety of the target.


1995 ◽  
Vol 36 (2) ◽  
pp. 267-268 ◽  
Author(s):  
Susumi Hatakeyama ◽  
Mitsuhiro Kawamura ◽  
Yasuko Mukugi ◽  
Hiroshi Irie
Keyword(s):  

Tetrahedron ◽  
2021 ◽  
Vol 82 ◽  
pp. 131928
Author(s):  
Mrinal K. Das ◽  
Abhinay Yadav ◽  
Satyajit Majumder ◽  
Ayan Mondal ◽  
Alakesh Bisai
Keyword(s):  

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