Regioselective Synthesis of Vinyl Halides, Vinyl Sulfones, and Alkynes: A Tandem Intermolecular Nucleophilic and Electrophilic Vinylation of Tosylhydrazones


Autoria(s): Ojha, Devi Prasan; Prabhu, Kandikere Ramaiah
Data(s)

2015

Resumo

A diazo species is trapped in an intermolecular fashion by two independent ion species in tandem at the carbene center to install an electrophile and a nucleophile on the same carbon. This metal-free concept, which is unprecedented, has been illustrated by regioselective synthesis of a variety of vinyl halides, vinyl sulfones, and alkyne derivatives.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/50805/1/org_let_17-1_18_2015.pdf

Ojha, Devi Prasan and Prabhu, Kandikere Ramaiah (2015) Regioselective Synthesis of Vinyl Halides, Vinyl Sulfones, and Alkynes: A Tandem Intermolecular Nucleophilic and Electrophilic Vinylation of Tosylhydrazones. In: ORGANIC LETTERS, 17 (1). pp. 18-21.

Publicador

AMER CHEMICAL SOC

Relação

http://dx.doi.org/10.1021/ol503114n

http://eprints.iisc.ernet.in/50805/

Palavras-Chave #Organic Chemistry
Tipo

Journal Article

PeerReviewed