Regioselective Synthesis of Vinyl Halides, Vinyl Sulfones, and Alkynes: A Tandem Intermolecular Nucleophilic and Electrophilic Vinylation of Tosylhydrazones
Data(s) |
2015
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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 |