| Literature DB >> 28654111 |
Saeed Balalaie1, Mohammad Shamakli2, Ali Nikbakht2, Nahid S Alavijeh2, Frank Rominger3, Shahnaz Rostamizadeh2, Hamid Reza Bijanzadeh4.
Abstract
A diversity-oriented access to isoxazolino and isoxazolo benzazepines is elaborated via a post-Ugi heteroannulation involving intramolecular 1,3-dipolar cycloaddition reaction of nitrile oxides with alkenes and alkynes. This sequence offers an interesting multicomponent entry to a library of isoxazolino and isoxazolo benzazepines under mild reaction conditions in good to excellent yields.Entities:
Year: 2017 PMID: 28654111 DOI: 10.1039/c7ob01142c
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876