A Convergent Synthesis of a Twelve-Membered Macrolide Natural Product, (6R,12S)-6-Hydroxy-12-methyl-1-oxacyclododecane-2,5-dione

2012 ◽  
Vol 95 (9) ◽  
pp. 1623-1629 ◽  
Author(s):  
Palakodety Radha Krishna ◽  
Pendyala Venkata Arun Kumar
2011 ◽  
Vol 13 (19) ◽  
pp. 5108-5111 ◽  
Author(s):  
Valer Jeso ◽  
Lisa Cherry ◽  
Todd K. Macklin ◽  
Subhas Chandra Pan ◽  
Philip V. LoGrasso ◽  
...  

Synlett ◽  
2012 ◽  
Vol 23 (06) ◽  
pp. 855-858 ◽  
Author(s):  
Margaret Brimble ◽  
Hui Geng ◽  
Jack Chen ◽  
Daniel Furkert ◽  
Shende Jiang

RSC Advances ◽  
2015 ◽  
Vol 5 (37) ◽  
pp. 29114-29120 ◽  
Author(s):  
Puli Saidhareddy ◽  
Arun K. Shaw

A convergent synthesis of macrolide natural product (−)-A26771B starting from d-glucal is reported. Key features of this synthesis involve Ferrier rearrangement, cross metathesis of chiral fragments 3 and 4 and Yamaguchi macrolactonization.


Author(s):  
Ardalan A. Nabi ◽  
Lydia M. Scott ◽  
Daniel P. Furkert ◽  
Jonathan Sperry

The rare benzoxazepine ring in the alkaloid inducamide C is unstable and prone to rearrangement, indicating that structural revision of the natural product may be necessary.


Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
V Myrianthopoulos ◽  
P Magiatis ◽  
AL Skaltsounis ◽  
L Meijer ◽  
E Mikros

Planta Medica ◽  
2012 ◽  
Vol 78 (05) ◽  
Author(s):  
SK Jain ◽  
R Sahu ◽  
J Zhang ◽  
MR Jacob ◽  
XC Li ◽  
...  

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