Catalytic Enantioselective 1,4-lodofunctionalizations of Conjugated Dienes
Data(s) |
2015
|
---|---|
Resumo |
The first catalytic enantioselective 1,4-iodofunctionalizations of conjugated dienes have been developed. Starting from beta,gamma,delta,epsilon-unsaturated oximes and 4-Ns hydrazones, these N-iodosuccinimide-mediated reactions are catalyzed by newly modified tertiary aminothiourea derivatives and furnish Delta(2)-isoxazoline and Delta(2)-pyrazoline derivatives, respectively, containing an (E)-allyl iodide group at the quaternary stereogenic center generally in high yield and with excellent enantioselectivity (up to 98.5:1.5 er). |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/52600/1/Org_Let_17-18_4424_2015.pdf Tripathi, Chandra Bhushan and Mukherjee, Santanu (2015) Catalytic Enantioselective 1,4-lodofunctionalizations of Conjugated Dienes. In: ORGANIC LETTERS, 17 (18). pp. 4424-4427. |
Publicador |
AMER CHEMICAL SOC |
Relação |
http://dx.doi.org/10.1021/acs.orglett.5b02026 http://eprints.iisc.ernet.in/52600/ |
Palavras-Chave | #Organic Chemistry |
Tipo |
Journal Article PeerReviewed |