Baudin, J. B.; Hareau, G.; Julia, S. A., Bulletin de la Societe Chimique de France, 1993, vol. 130, p. 856 - 878
作者:Baudin, J. B.、Hareau, G.、Julia, S. A.、Lorne, R.、Ruel, O.
DOI:——
日期:——
Chuang, Che-Ping; Ngoi, Tak Ho Johnny, Journal of Chemical Research, Miniprint, 1991, # 1, p. 115 - 123
作者:Chuang, Che-Ping、Ngoi, Tak Ho Johnny
DOI:——
日期:——
Investigation of the halocyclization of S- and N-allyl derivatives of 2-benzothiazolethione
作者:D. G. Kim、N. M. Sudolova、P. A. Slepuhin
DOI:10.1007/s10593-011-0808-y
日期:2011.8
3-Allyl-2-benzothiazolethione reacts with iodine regiospecifically with annelation of the five-membered ring, while with bromine a mixture of the five- and six-membered rings are formed. 2-Allylthiobenzothiazole reacts with halogens with annelation of the five- and six-membered rings, while 2-(2-methyl-2-propenyl)thiobenzothiazole is annelated at the five-membered ring.
A Practical Access to Functionalized Alkyl Sulfinates
of aliphatic sulfinates. This cost-effective method involves the use of 2-mercaptobenzothiazole under mild conditions and exhibits good yields (up to 78% over three steps). This approach provides an access to a wide range of functionalized sulfinates. A good tolerance with respect to diverse functional groups (alkene, alkyne, ether, acetal) was also noted.