Oxidative benzoin reactions

J. Castells; F. Pujol; H. Llitjós; M. Moreno-Mañas

doi:10.1016/0040-4020(82)80170-1

Oxidative benzoin reactions

J. Castells, F. Pujol, H. Llitjós, M. Moreno-Mañas

Departamento de Química

Producción científica: Contribución a una revista › Artículo › Investigación › revisión exhaustiva

51 Citas (Scopus)

Resumen

A one-pot synthesis (yields over 50%) of methyl and ethyl esters from aldehydes (and the corresponding alcohol), using aromatic nitrocompounds as oxidizing agents under the catalytic action of cyanide ion or of a conjugate base of a thiazolium ion, is described. A variety of by-products (α-hydroxybenzylidenaniline) (16), α-methoxybenzylidenaniline (21), α-cyanobenzylidenaniline (27), N1-hydroxy-N1,N2-diphenylbenzamidine (28), and others) have been identified. © 1982.

Idioma original	Inglés
Páginas (desde-hasta)	337-346
Publicación	Tetrahedron
Volumen	38
N.º	3
DOI	https://doi.org/10.1016/0040-4020(82)80170-1
Estado	Publicada - 1 ene 1982

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title = "Oxidative benzoin reactions",

abstract = "A one-pot synthesis (yields over 50\%) of methyl and ethyl esters from aldehydes (and the corresponding alcohol), using aromatic nitrocompounds as oxidizing agents under the catalytic action of cyanide ion or of a conjugate base of a thiazolium ion, is described. A variety of by-products (α-hydroxybenzylidenaniline) (16), α-methoxybenzylidenaniline (21), α-cyanobenzylidenaniline (27), N1-hydroxy-N1,N2-diphenylbenzamidine (28), and others) have been identified. {\textcopyright} 1982.",

author = "J. Castells and F. Pujol and H. Llitj{\'o}s and M. Moreno-Ma{\~n}as",

year = "1982",

month = jan,

day = "1",

doi = "10.1016/0040-4020(82)80170-1",

language = "English",

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T1 - Oxidative benzoin reactions

AU - Castells, J.

AU - Pujol, F.

AU - Llitjós, H.

AU - Moreno-Mañas, M.

PY - 1982/1/1

Y1 - 1982/1/1

N2 - A one-pot synthesis (yields over 50%) of methyl and ethyl esters from aldehydes (and the corresponding alcohol), using aromatic nitrocompounds as oxidizing agents under the catalytic action of cyanide ion or of a conjugate base of a thiazolium ion, is described. A variety of by-products (α-hydroxybenzylidenaniline) (16), α-methoxybenzylidenaniline (21), α-cyanobenzylidenaniline (27), N1-hydroxy-N1,N2-diphenylbenzamidine (28), and others) have been identified. © 1982.

AB - A one-pot synthesis (yields over 50%) of methyl and ethyl esters from aldehydes (and the corresponding alcohol), using aromatic nitrocompounds as oxidizing agents under the catalytic action of cyanide ion or of a conjugate base of a thiazolium ion, is described. A variety of by-products (α-hydroxybenzylidenaniline) (16), α-methoxybenzylidenaniline (21), α-cyanobenzylidenaniline (27), N1-hydroxy-N1,N2-diphenylbenzamidine (28), and others) have been identified. © 1982.

UR - https://www.scopus.com/pages/publications/0012045720

U2 - 10.1016/0040-4020(82)80170-1

DO - 10.1016/0040-4020(82)80170-1

M3 - Article

SN - 0040-4020

VL - 38

SP - 337

EP - 346

JO - Tetrahedron

JF - Tetrahedron

IS - 3

ER -

Oxidative benzoin reactions

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Huella

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