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PERKOW Vinyl phosphate synthesis

Enol phosphate synthesis from a-halocaiboityls and trialkylphosphites. General scheme  [Pg.470]

X = Cl, Br, I, secondary or tertiary halides are reqnired to retard the competing Michaelis-Arbuzov reaction. [Pg.470]

Name Reactions A Collection of Detailed Mechanisms and Synthetic Applications, DOI 10.1007/978-3-319-03979-4 210, Springer International Publishing Switzerland 2014 [Pg.470]

Borowitz, G. B. Borowitz, I. J. Handb. Organophosphorus Chem. 1992, 115. (Review). [Pg.471]

Balasubramanian, M. Perkow Reaction, in Name Reactions for Functional Group Transformations, Li, J. J. Ed., Wiley Hoboken, NJ, 2007, pp 369-385. (Review). CofFmier, D. El Kaim, L. Grimaud, L. Org. Lett. 2009,11, 1825-1827. [Pg.471]

PERKIN Carboxyle acid(estar) synthesis 293 PERKIN Coumann rearrangement 293 PERKOW Vinyl phosphate synthesis 294... [Pg.226]

See other pages where PERKOW Vinyl phosphate synthesis is mentioned: [Pg.333]    [Pg.766]    [Pg.470]    [Pg.810]    [Pg.307]    [Pg.678]    [Pg.333]    [Pg.766]    [Pg.470]    [Pg.810]    [Pg.307]    [Pg.678]    [Pg.16]    [Pg.2168]   
See also in sourсe #XX -- [ Pg.294 ]

See also in sourсe #XX -- [ Pg.286 ]

See also in sourсe #XX -- [ Pg.286 ]



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