z-logo
Premium
Aqueous‐Mediated green synthesis of novel spiro[indole‐quinazoline] derivatives using kit‐6 mesoporous silica coated Fe 3 O 4 nanoparticles as catalyst
Author(s) -
Abdolmohammadi Shahrzad,
Shariati Shahab,
Fard Narges Elmi,
Samani Amir
Publication year - 2020
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.3981
Subject(s) - chemistry , catalysis , mesoporous material , mesoporous silica , aqueous solution , indole test , nanoparticle , guanidine , aqueous medium , green chemistry , combinatorial chemistry , organic chemistry , nuclear chemistry , chemical engineering , reaction mechanism , engineering
In this work, a series of eight new spiro[3,4′]1,3‐dihydro‐2 H ‐indol‐2‐one‐2′‐amino‐4′,6′,7′,8′‐tetrahydro‐2′,5’(1’ H ,3’ H )‐quinazoline‐diones were successfully synthesized through a three‐component reaction of 1 H ‐indole‐2,3‐diones (isatins), guanidine nitrate, and 1,3‐cyclohexanediones, by use of Kit‐6 mesoporous silica coated Fe 3 O 4 nanoparticles (Fe 3 O 4 @SiO 2 @KIT‐6) as a highly efficient magnetically separable nanocatalyst in aqueous media at 60°C. Several notable features of thiseco‐friendly protocol are high yields of products, short reaction times, operational simplicity, and the use of easily available and recyclable catalyst.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here