Reductive Cleavage of 4'H-Spiro[indole-3,5'-isoxazoles] En Route to 2-(1H-Indol-3-yl)acetamides with Anticancer Activities.
J Org Chem
; 87(21): 13955-13964, 2022 11 04.
Article
in En
| MEDLINE
| ID: mdl-36260110
ABSTRACT
Unusual cascade transformation involving ring opening and 1,2-alkyl shift was observed upon the reduction of 4'H-spiro[indole-3,5'-isoxazoles] or 2-(3-oxoindolin-2-yl)acetonitriles with sodium borohydride. This reaction allowed for expeditious and highly efficient preparation of 2-(1H-Indol-3-yl)acetamides with antiproliferative properties.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Isoxazoles
/
Acetamides
Language:
En
Journal:
J Org Chem
Year:
2022
Type:
Article