Journal of Organic Chemistry p. 4799 - 4805 (1985)
Update date:2022-08-02
Topics:
Singh, Sharat
Nimmesgern, Hildegard
Schaumann, Ernst
Ramamurthy, Vaidhyanathan
The higher excited-state reactions of sterically encumbered thioketenes 1a-d in solution were investigated.Substituted thiiranes, thio esters, thioacetophenones, and 1,2-diones are formed on photoexcitation of thioketenes in hydroxylic and nonhydroxylic solvents.Thioketenes while unreactive upon excitation to S1 produce thiiranylidene carbene and zwitterionic intermediates upon excitation to S2.The reactive state is identified to be S2 (??*).The excited thioketene resists carbon monosulfide elimination but undergoes rearrangement.The photobehavior of thioketenes, established in solution for the first time, differs significantly from that of ketenes, and it cannot be extrapolated from that of structurally analogous ketenes and allenes.
View MoreChangzhou Anyi Biochem Co., Ltd.(expird)
Contact:+86-519-88836158
Address:no,51 caoda
Shangyu Sanhechemicals Co.,LTD.
Contact:86-0571-56696839
Address:Num.2952,Nanhuan Road,Binjiang District,Hangzhou,China
Chengdu Cogon Bio-tech Co., Ltd.
Contact:86-28-85171192
Address:NO.52.YongFeng Rd. Chengdu,610041,P.R.China.
Zhejiang Allied Chemical Co.,Ltd
Contact:18967038207
Address:Area A-30, High-tech Industrial Park, Quzhou, Zhejiang, China.
Contact:0086-29-89196322
Address:North of the Fifth Keji Road, Hi-Tech Industrial Zone, Xi'an City, Shaanxi Province, China
Doi:10.1021/jo01056a067
(1962)Doi:10.1021/ja01992a004
(1904)Doi:10.1016/j.tet.2006.10.030
(2007)Doi:10.1016/0957-4166(95)00003-8
(1995)Doi:10.1021/jo00271a023
(1989)Doi:10.1002/chem.201805530
(2019)