Big Chemical Encyclopedia

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

Articles Figures Tables About

Eliminations alkynes

The phosphonite 81 was shown to render a phosphonium salt 84 by interaction with the primarily obtained N-acyliminium salt 83. Deprotonation transformed 84 to the oxaphosphohdine 85, which undergoes l,3-dipolar cycloaddition with the activated alkyne elimination of phosphonate from the adduct 86 gives rise to the pyrrole system 82. In contrast to Mtinchnones (cf. p. 175), the mesoionic 1,3-dipoles of type 85 show high regioselectivity in the cycloaddition process. [Pg.123]

Naming Alkynes Preparation of Alkynes Elimination Reactions of Dihalides... [Pg.314]


See other pages where Eliminations alkynes is mentioned: [Pg.261]    [Pg.297]    [Pg.261]    [Pg.671]    [Pg.277]    [Pg.297]    [Pg.297]    [Pg.261]    [Pg.89]    [Pg.277]    [Pg.277]    [Pg.52]    [Pg.316]    [Pg.185]   
See also in sourсe #XX -- [ Pg.398 ]




SEARCH



Alkyne derivatives reductive elimination

Alkyne-forming eliminations

Alkynes by elimination

Alkynes by elimination reactions

Alkynes double elimination from dihaloalkanes

Alkynes elimination with boranes

Alkynes via E2 Elimination

Cyclic alkynes from elimination reactions

Diethyl alkyne elimination

Double elimination, alkyne preparation

E2 elimination from vinyl halides how to make alkynes

Elimination alkyne synthesis

Elimination reactions alkyne synthesis

Elimination reactions alkynes

Elimination reactions alkynes from

Elimination reactions synthesis of alkynes

Elimination reactions, cyclic alkynes

Elimination to Give Alkynes

Eliminations giving alkynes

Ethanol, alkyne elimination

Methanol alkyne elimination

Preparation of Alkynes by Double Elimination

Preparation of Alkynes by Elimination Reactions

Synthesis of Alkynes by Elimination Reactions

© 2024 chempedia.info