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(DHQ)2AQN-catalyzed asymmetric substitution of isatin-derived hydrazones with O-Boc-protected Morita-Baylis-Hillman adducts: A strategy for synthesizing enantioenriched azo compounds incorporating an oxindole scaffold.
Yang, Hai-Bin; Zhao, Yun-Zhou; Sang, Rui; Shi, Min.
  • Yang HB; State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , 345 Lingling Road, Shanghai 200032, China.
J Org Chem ; 79(8): 3519-28, 2014 Apr 18.
Article en En | MEDLINE | ID: mdl-24670223
ABSTRACT
The first example for the preparation of enantioenriched azo compounds from hydrazones and Morita-Baylis-Hillman adducts has been developed, affording azo compounds incorporating an oxindole scaffold in up to 91% yield along with a 93% ee value under the catalysis of (DHQ)2AQN.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Compuestos Azo / Antraquinonas / Éteres / Hidrazonas / Indoles / Isatina Idioma: En Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Compuestos Azo / Antraquinonas / Éteres / Hidrazonas / Indoles / Isatina Idioma: En Año: 2014 Tipo del documento: Article