Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Harold Coates"'
Publikováno v:
Phosphorous and Sulfur and the Related Elements. 6:481-488
The reaction between finely divided white phosphorus and several alkoxide ions in the presence of tetrachloromethane and excess of alcohol has been investigated under a variety of conditions. High yields of trialkylphosphite are obtained when two equ
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :599-603
Esters of the title compound have been obtained by rearrangement of aroyl penicillanoyl peroxides, followed by decarboxylation. Certain of the aroyl esters so produced have been epimerised at position 6 with selected secondary amines. Conditions for
Publikováno v:
ACS Symposium Series ISBN: 9780841206632
Phosphorus Chemistry: Proceedings of the 1981 International Conference
Phosphorus Chemistry: Proceedings of the 1981 International Conference
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2aa9e76e7f691118d8bbd3f51057665
https://doi.org/10.1021/bk-1981-0171.ch047
https://doi.org/10.1021/bk-1981-0171.ch047
Publikováno v:
Chemischer Informationsdienst. 9
Trialkyl phosphites can be prepared in high yield by direct reaction of alkoxide ion with elemental phosphorus in the presence of tetrachloromethane.
Autor:
Harold Coates
Publikováno v:
The Lancet. 157:499-500
n/a
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1459
The sulphenic acid intermediates produced thermally from penicillin S-oxides undergo addition to acetylenic esters to produce conjugated sulphoxides in good yields. These vinylic sulphoxides are subject to nucleophilic addition reactions, with, for e
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :7
Trialkyl phosphites can be prepared in high yield by direct reaction of alkoxide ion with elemental phosphorus in the presence of tetrachloromethane.
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :303
The sulphenic acid intermediates produced thermally from penicillin sulphoxides can be added across acetylenic esters to produce conjugated sulphoxides in good yield.