Premium
Synthesis of Highly Z ‐Selective Coumarin Annulated Dioxocine, Dioxacindione and Macrocycles Using Grubbs’ Second‐Generation Catalyst
Author(s) -
Goud E. Yadaiah,
Rao B. Kanakadurga,
Thirupahi G.,
Hemasri Y.,
Rao Ch. Prasad,
Kumar P. Vijay,
Rao Y. Jayaprakash
Publication year - 2017
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.201601614
Subject(s) - coumarin , ring closing metathesis , metathesis , intramolecular force , ring (chemistry) , chemistry , catalysis , combinatorial chemistry , grubbs' catalyst , tricyclic , salt metathesis reaction , stereochemistry , organic chemistry , polymerization , polymer
Abstract The diversity‐oriented organic synthesis of novel coumarin annulated tricyclic dioxocine, dioxacindione scaffolds with Z ‐selectivity and the symmetrical pentacyclic coumarin macrocyclic derivatives is demonstrated from substituted hydroxyl coumarins via ring‐closing metathesis in the presence of Grubbs’ second‐generation catalyst as the facile and efficient route with excellent yields. This synthetic strategy provides a route for the intramolecular ring‐closing metathesis to access a library of novel tricyclic coumarin heterocycles and pentacyclic coumarin macrocycles having different ring systems.