Chemistry of Heterocyclic Compounds p. 728 - 733 (1984)
Update date:2022-08-03
Topics:
Klimenko, S. K.
Stolbova, T. V.
Tyrina, T. I.
Sorokin, N. N.
Leshcheva, I. F.
et al.
The structure of aryl-substituted cis-1-thiadecalins formed together with 5,6-tetramethylenethiopyrylium salts in disproportionation reactions of condensed 4H-, 6H-thiopyrans and dihydrothiopyrans with CF3COOH, as well as in the ionic reduction of the latter by the ion pair trifluoroacetic acid-triethylsilane, was studied.It was shown that the reduction proceeds stereospecifically with the formation of configurationally and conformationally homogeneous aryl-cis-1-thiadecalins possessing 2α-R1- and 2α-R1-4α-R2-configurations.The configurational and conformational assignments were made by the 13C NMR method.
View MoreShandong Hongxiang Zinc Co., Ltd
Contact:086-0311-66187879
Address:DaWang developing zone
Contact:86-571-86737118-8689
Address:No.69, 12 Street, HEDA, Hangzhou, Zhejiang, China
Taizhou Shengxing Chempharm Co.,Ltd
Contact:+86-576-88516600
Address:Yantou Chemical Zone Jiaojiang Taizhou Zhejiang China
suzhou chukai pharmateach co,.ltd
Contact:86-512-88812511
Address:Building 3, Wujiang Scientific Innovation Park, 2358 Changan Rd, Wujiang 215200, Jiangsu Province, P. R. China
Luzhou North Chemical Co., Ltd.
Contact:+86-830-2796784；+86-830-2796776
Address:Gaoba, Longmatan District, Luzhou, Sichuan Province
Doi:10.1039/b616884a
(2007)Doi:10.1016/j.bmcl.2007.04.084
(2007)Doi:10.1039/c39870001714
(1987)Doi:10.1021/jo00255a007
(1988)Doi:10.1016/j.jorganchem.2009.01.005
(2009)Doi:10.1021/ja00230a025
(1988)
