Synthetic studies in the oxytocin field. III. An alternative synthesis of oxytocin

1956 ◽  
Vol 21 (1) ◽  
pp. 202-210 ◽  
Author(s):  
J. Rudinger ◽  
J. Honzl ◽  
M. Zaoral
Keyword(s):  
Alternative Synthesis ◽  
Synthetic Studies

Synthetic studies toward the anthrax tetrasaccharide: alternative synthesis of this antigen

2012 ◽  
Vol 356 ◽  
pp. 115-131 ◽  
Author(s):  
Ophélie Milhomme ◽  
Sandrine G.Y. Dhénin ◽  
Florence Djedaïni-Pilard ◽  
Vincent Moreau ◽  
Cyrille Grandjean
Keyword(s):  
Alternative Synthesis ◽  
Synthetic Studies

Synthetic studies on (2R,4'R,8'R)-.alpha.-tocopherol. An alternative synthesis of (2R,6R)-(+)-2,6,10-trimethylundecan-1-ol, a key side chain synthon

1976 ◽  
Vol 41 (22) ◽  
pp. 3512-3515 ◽  
Author(s):  
Noal. Cohen ◽  
Wayne F. Eichel ◽  
Rocco J. Lopresti ◽  
Christian. Neukom ◽  
Gabriel. Saucy
Keyword(s):  
Alpha Tocopherol ◽  
Side Chain ◽  
Alternative Synthesis ◽  
Synthetic Studies

Synthetic studies toward inducamide C

2021 ◽  
Author(s):  
Ardalan A. Nabi ◽  
Lydia M. Scott ◽  
Daniel P. Furkert ◽  
Jonathan Sperry
Keyword(s):  
Natural Product ◽  
Structural Revision ◽  
Synthetic Studies

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.

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