
Bulletin of the Chemical Society of Japan p. 1101 - 1104 (1981)
Update date:2022-08-02
Topics:
Nanasawa, Masato
Kamogawa, Hiroyoshi
The title effect has been investigated with the imidazolyl group either externally added or intramolecularly combined.N-Retinylidenebutylamine was protonated with imidazole derivatives under neutral conditions and was absorbed at longer wavelengths compared with carboxylic acids.The absorption peak with the imidazolyl group intramolecularly combined was highly affected by the structure, protonated Nα-retinylidene-L-histidine octadecylamide having an absorption maximum at 494 nm caused by the inductive effect and the polar imidazolyl group.
View Morewebsite:http://www.eastarchem.com/
Contact:1-800-898-2436
Address:1215 K Street, STE 1700
website:http://www.acrospharmatech.com
Contact:+1-3234804688
Address:Flat/RM 1502,Easey Commercial building 253-261 Hennessy Road,Wanchai,HongKong
Lanzhou huibang biological chemical technology Co., LTD
Contact:0931-7843964
Address:NO.2011,Yannan Road,Chengguan,
Contact:
Address:
Lishui Nanming Chemical Co., Ltd(expird)
Contact:+86-0578-2134101,2697830
Address:No.19 Tongji Road Shuige Industrial zone
Doi:10.1055/s-1981-29580
(1981)Doi:10.1021/jo00332a004
(1981)Doi:10.1021/jacs.6b01939
(2016)Doi:10.1021/ja0459781
(2004)Doi:10.1021/jm00141a009
(1981)Doi:10.1080/15533174.2016.1158186
(2017)