Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Stereoselective synthesis single bond additions

The double bond of butenolides undergoes stereoselective Michael addition of organometallic reagents, affording useful synthetic intermediates. Thus 1,4-addition of lithium dimethylcuprate to 231 gave 236 as a single isomer, which was employed (237) for the synthesis of the bromopentene derivative 237. [Pg.184]

See other pages where Stereoselective synthesis single bond additions is mentioned: [Pg.440]    [Pg.861]    [Pg.80]    [Pg.23]    [Pg.440]    [Pg.1032]    [Pg.341]    [Pg.520]    [Pg.861]    [Pg.440]    [Pg.23]    [Pg.126]    [Pg.246]    [Pg.344]    [Pg.176]    [Pg.179]    [Pg.187]    [Pg.118]    [Pg.32]    [Pg.483]    [Pg.17]    [Pg.299]    [Pg.270]    [Pg.78]    [Pg.260]    [Pg.132]    [Pg.284]    [Pg.385]    [Pg.988]    [Pg.215]    [Pg.1362]    [Pg.230]    [Pg.259]    [Pg.988]    [Pg.940]    [Pg.121]    [Pg.405]    [Pg.786]    [Pg.342]    [Pg.1]    [Pg.260]    [Pg.89]    [Pg.184]    [Pg.258]    [Pg.433]    [Pg.21]    [Pg.647]    [Pg.159]    [Pg.259]   
See also in sourсe #XX -- [ Pg.671 ]



SEARCH



Addition stereoselective

Addition synthesis

Additive synthesis

Bonding single bonds

Bonds synthesis

Single bonds

Single synthesis

Stereoselective synthesis

Stereoselectivity addition

Stereoselectivity synthesis

© 2024 chempedia.info