SmI2-mediated reduction of gamma,gamma-difluoro-alpha,beta-enoates with application to the synthesis of functionalized (Z)-fluoroalkene-type dipeptide isosteres.
Otaka, Akira
SmI2-mediated reduction of gamma,gamma-difluoro-alpha,beta-enoates with application to the synthesis of functionalized (Z)-fluoroalkene-type dipeptide isosteres. [electronic resource] - The Journal of organic chemistry Mar 2004 - 1634-45 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0022-3263
10.1021/jo035709d doi
Alkenes--chemistry
Dipeptides--chemical synthesis
Hydrocarbons, Fluorinated--chemical synthesis
Imines--chemistry
Iodides--chemistry
Magnetic Resonance Spectroscopy
Molecular Structure
Samarium--chemistry
Stereoisomerism
SmI2-mediated reduction of gamma,gamma-difluoro-alpha,beta-enoates with application to the synthesis of functionalized (Z)-fluoroalkene-type dipeptide isosteres. [electronic resource] - The Journal of organic chemistry Mar 2004 - 1634-45 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0022-3263
10.1021/jo035709d doi
Alkenes--chemistry
Dipeptides--chemical synthesis
Hydrocarbons, Fluorinated--chemical synthesis
Imines--chemistry
Iodides--chemistry
Magnetic Resonance Spectroscopy
Molecular Structure
Samarium--chemistry
Stereoisomerism