Chemistry of Heterocyclic Compounds p. 191 - 194 (1987)
Update date:2022-07-29
Topics:
Degutis, Yu. A.
Shachkus, A. A.
When derivatives of 1,2,3,9a-tetrahydro-9H-imidazo<1,2-a>indol-2-one or 1-carbamoylmethyl-2-methylene-2,3-dihydroindole are reacted with lithium aluminium hydride, derivatives of 1,2,3,9a-tetrahydro-9H-imidazo<1,2-a>indole are formed.Under the same conditions 1-(N-phenylcarbamoylmethyl)-2-methylene-2,3-dihydroindole is not cyclized to an imidazo<1,2-a)indole.When treated with proton acids imidazo<1,2-a>indoles are converted to 3H-indolium salts.Opening of the imidazolidine ring is also found when imidazo<1,2-a>indole is acylated with benzoyl chloride.
View MoreWeifang Adde Economic And Trade Co.,LTD.
Contact:86-536-8885548
Address:Room 1402,Wanda Plaza B Block,No.958,Yuanfei Road,Kuiwen District
TIANJIN DONGRUXIANG MINERALS MARKETING CO.,LTD(expird)
Contact:22-58516360
Address:tianjin
Tianjin Realet Chemical Technology Co.,Ltd.
website:http://www.realetchem.com
Contact:+86-022-58788819
Address:shuanggang industrial park
Shenyang Xinyihan Chemical Technology Co., Ltd.
Contact:+86-18525026267
Address:362, aigongbeijei street 23 , tiexi district,Shenyang, Liaoning, China
Antaeus Bio-technology Co., LTD(expird)
Contact:021-31252569
Address:shanghai pudong
Doi:10.1021/ic801836k
(2009)Doi:10.1016/S0040-4039(00)85430-1
(1986)Doi:10.1016/S0040-4039(00)87791-6
(1986)Doi:10.1039/b821534k
(2009)Doi:10.1002/anie.202107860
(2021)Doi:10.1021/ja00258a063
(1987)
