Modular Access to Highly Functionalised Tetrahydroquinolines | Zendy

Cordero Franca M. | Zendy; Khairnar Bhushan B. | Zendy; Brandi Alberto | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Modular Access to Highly Functionalised Tetrahydroquinolines

Author(s) -

Cordero Franca M.,

Khairnar Bhushan B.,

Brandi Alberto

Publication year - 2014

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201403025

Subject(s) - chemistry , nitrone , cycloaddition , combinatorial chemistry , cleavage (geology) , modular design , stereochemistry , organic chemistry , catalysis , computer science , geotechnical engineering , fracture (geology) , engineering , operating system

Highly functionalised tetrahydroquinolines have been obtained by a modular approach consisting of a nitrone 1,3‐dipolar cycloaddition to 2‐bromostyrene followed by isoxazolidine N–O cleavage and copper‐catalysed aromatic N ‐substitution/cyclisation. A 1,2,3,4‐tetrahydro‐1,8‐naphthyridine was obtained in the same way.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research