Catalytic Enantioselective 1,4-lodofunctionalizations of Conjugated Dienes


Autoria(s): Tripathi, Chandra Bhushan; Mukherjee, Santanu
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