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Platinum‐Catalyzed Tandem Cyclization Reaction to Multiply Substituted Indolines under Microwave‐Assisted Conditions
Author(s) -
Ma CanLiang,
Yu XiaoLong,
Zhu XiaoLong,
Hu YongZhou,
Dong XiaoWu,
Tan Bin,
Liu XinYuan
Publication year - 2015
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201400933
Subject(s) - chemistry , hydroamination , tandem , catalysis , intramolecular force , cascade reaction , platinum , intermolecular force , transfer hydrogenation , combinatorial chemistry , aldol condensation , microwave irradiation , photochemistry , organic chemistry , ruthenium , molecule , materials science , composite material
A convenient platinum‐catalyzed tandem cyclization reaction from readily available aminoalkynes and enones has been developed to efficiently prepare multiply substituted indolines in good yields under microwave irradiation within a short reaction time. This efficient reaction is presumed to proceed via a tandem process involving intramolecular hydroamination of aminoalkynes, Michael addition of enones, aldol condensation and intermolecular transfer hydrogenation.