Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 101 - 107 (1990)
Update date:2022-08-02
Topics:
Smolyakova, I. P.
Smit, V. A.
Lutsenko, A. I.
Daeva, E. D.
Reaction of methoxyallene with arylsulphenyl chlorides proceeds nonselectively with formation of mixtures of 1,2- and 2,3-arylthiochloro adducts, the composition of which depends on the nature of the reagent and solvent. ?-Donating compounds of various types in the presence of Lewis acids are alkylated by adducts of methoxyallene with arylsulphenyl chlorides and primarily products are formed by attack at the C3 atom of the reagent.
View MoreContact:86-571-86737118-8689
Address:No.69, 12 Street, HEDA, Hangzhou, Zhejiang, China
Jinan Hongfangde Pharmatech Co.LTD
Contact:0531-88870908
Address:F Bldg,750#,Shunhua Rd,New&High-tech Zone,Jinan,Shandong,China 250101
KA-SHING Business Trade Macau Co., Ltd.
Contact:00853-28430045
Address:23rd Floor, Block 3 La Cite, Areia Preta, Macao
website:http://www.chinabarton.com
Contact:+86-573-82719618
Address:No. 162 Fumin Road, Honghe Town,
Taizhou Chemedir Biopharm-tech Co., Ltd
Contact:+86 523 86200218
Address:G09, No. 1 Avenue China Medical City, Taizhou,Jiangsu, China
Doi:10.1021/ol200676k
(2011)Doi:10.1021/ml100200c
(2010)Doi:10.1007/s12039-015-1020-x
(2016)Doi:10.1002/1099-0690(200202)2002:4<614::AID-EJOC614>3.0.CO;2-Q
(2002)Doi:10.1002/chem.201002789
(2011)Doi:10.1021/acs.joc.6b01016
(2016)
