Big Chemical Encyclopedia

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

Articles Figures Tables About

Barton-Kellogg olefination

BARTON - KELLOGG Olefination 25 BARTON - McCOMBIE Deoxyqenation 26 BAUDISCH Nitrosophenol synthesis 27 Bauer 156... [Pg.223]

BARTON KELLOGG Olefination Olefin synthesis (tetrasubsMuted) from hydrazones and thioKetones via a3-1,3,4-thiadiazolines. [Pg.246]

Barton-Kellogg Olefin Synthesis Barton-Kellogg Reaction)... [Pg.249]

Wang Z. Barton-Kellogg Olefination. Comprehensive organic name reactions and reagents. Wiley... [Pg.372]

Known as Barton-Kellogg olefination, C=C bond formation by the reaction of a thioketone and a ketone through a diazo intermediate has been pioneered by Staudinger s group and further developed by the groups of Barton and Kellogg [22-24]. The thioketone required for the reaction is commonly derived from a... [Pg.241]

BARTON KELLOGG Olefinalion Olefin synthesis (letrasubsirtuted) from hydrazones and thiokelones via A -f,3,4-Ihiadiazollnes. [Pg.25]

BARTON - KELLOGG Olefinalwn Olefin synthesis (tetrasubstituted) from hydrazones and thioketones via A3-1,3,4-... [Pg.246]

See other pages where Barton-Kellogg olefination is mentioned: [Pg.249]    [Pg.249]    [Pg.250]    [Pg.252]    [Pg.51]    [Pg.242]    [Pg.249]    [Pg.249]    [Pg.250]    [Pg.252]    [Pg.51]    [Pg.242]   
See also in sourсe #XX -- [ Pg.35 ]



SEARCH



Barton

© 2024 chempedia.info