
Chemistry Letters p. 1007 - 1010 (1994)
Update date:2022-08-03
Topics:
Furukawa, Naomichi
Fujii, Takayoshi
Kimura, Takeshi
Fujihara, Hisashi
Naphthalene-1,8-dithiol reacted with aldehydes to give dithioacetals which were oxidized to 2-substituted naphtho<1,8-de>1,3-dithiin-1-oxides (4). 2,2-Disubstituted naphtho<1,8-de>1,3-dithiin-1-oxides (5) were obtained on treatment of 4 with NaH/electrophiles.Photolysis of 4 and 5 undergoes intramolecular oxygen rearrangement to generate aldehydes and ketones quantitatively together with naphthalene-1,8-dithiole.
View MoreAnhui Sunsing Chemicals Co.,Ltd
website:http://www.sunsingchem.com
Contact:0086-566-2023179
Address:Jin An industry park, Chizhou economic technical development zone, Anhui
Jiaozuo Zhongwei Special Products Pharmaceutical Co.,Ltd.
website:http://www.zw-pvp.com
Contact:15302105619
Address:Jiaozuo,Henan,China (Mainland)
MTT Pharma & Bio-technology Co.,Ltd(expird)
Contact:+86-21-58407925
Address:Room2019, Building C, Tomson Center, No.158, Zhang Yang Road, Shanghai, China
Contact:+86+21-58956006 15800617331
Address:402 Room, 150# Cailun Road, Zhangjiang high tech park, Shanghai
Haitong Chemical Industrial Co.,Ltd.
website:https://www.haitonglongwin.com/
Contact:+86-022-66221018
Address:18-701, No.99, The 4th Street, TEDA,
Doi:10.1063/1.1315996
(2000)Doi:10.1134/S1070428018100019
(2018)Doi:10.1002/(SICI)1096-9888(199812)33:12<1256::AID-JMS748>3.0.CO;2-Z
(1998)Doi:10.1111/j.2042-7158.1965.tb07635.x
(1965)Doi:10.1016/j.ejmech.2017.05.002
(2017)Doi:10.1021/jo00822a013
(1971)