Synthesis of Nitroethylindole Derivatives through Michael Addition

被引：0
作者：
Vani, Inavolu [1 ]
Sireesha, Reddymasu [2 ]
Goud, Palle Vinod Kumar [3 ]
Prasad, Kottapalli Rajasekhara [1 ]
Tej, Mandava Bhuvan [4 ]
Praneeth, Muthineni Sai [5 ]
Rao, Mandava Venkata Basaveswara [6 ]
机构：
[1] Koneru Lakshmaiah Educ Fdn, Dept Chem, Vaddeswaram, Andhra Pradesh, India
[2] Acharya Nagarjuna Univ, Dept Chem, Nagarjuna Nagar, Andhra Pradesh, India
[3] Govt Degree Coll, Dept Chem, Kukatpally, Telangana, India
[4] Sri Ramachandra Inst Higher Educ & Res, Dept Pharm, Chennai, Tamil Nadu, India
[5] Mamata Med Coll, Dept Pharm, Final MBBS Part 2, Khammam, Telangana, India
[6] Krishna Univ, Dept Chem, Machilipatnam, Andhra Pradesh, India
来源：
POLYCYCLIC AROMATIC COMPOUNDS | 2022年 / 42卷 / 10期
关键词：
Indole; michael addition; microwave irradiation; nitrostyrene; FRIEDEL-CRAFTS ALKYLATION; CATALYST; INDOLES; CYCLIZATION; MANAGEMENT; EFFICIENT; GREEN;
D O I：
10.1080/10406638.2021.1995009
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A series of nitroethylindole derivatives (3a-h) have been synthesized by Michael addition reaction between Indole and substituted nitrostyrenes in good yields under both conventional as well as microwave irradiation protocols. All the newly synthesized nitroethyl indole derivatives were characterized by H-1 NMR, C-13 NMR, and LC-MS analysis data.
引用
收藏
页码：7025 / 7033
页数：9
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