In:
Chemistry – An Asian Journal, Wiley, Vol. 16, No. 20 ( 2021-10-18), p. 3179-3187
Abstract:
An efficient synthetic method for structurally various isochromenoindolones has been demonstrated through Rh(III)‐catalyzed C−H activation followed by a cyclization reaction of N ‐methoxyarylamides with 3‐diazooxindoles. The sequential reaction involves the streamlined formation of C−C and C−O bonds in one pot. The present method provides a broad range of isochromenoindolones as a new privileged scaffold in moderate to good yields with the release of methoxyamine and molecular nitrogen and has the benefits of a broad substrate scope and good functional group tolerance.
Type of Medium:
Online Resource
ISSN:
1861-4728
,
1861-471X
DOI:
10.1002/asia.202100797
Language:
English
Publisher:
Wiley
Publication Date:
2021
detail.hit.zdb_id:
2233006-9