Synthesis of 5,6-dihydro-2H-thiins and 2,3-dihydro-1,4-oxathiins based on 1-benzylsulfonyl-1,1-dihydropolyfluoroalkan-2-ones

被引:6
作者
Yemets, SV [1 ]
Bandera, YP [1 ]
Timoshenko, VM [1 ]
Shermolvich, YG [1 ]
机构
[1] Natl Acad Sci Ukraine, Inst Organ Chem, UA-02094 Kiev 94, Ukraine
关键词
polyfluoroalkyl ketone; phthalimidosulfenyl chloride; succinimidosulfenyl chlorides; alpha-thioxoketone; thiin; oxathiin;
D O I
10.1016/S0022-1139(02)00061-1
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
1-Benzylsulfonyl-1,1-dihydropolyfluoroalkan-2-ones react with phthalimidosulfenyl chloride or succinimidosulfenyl chloride to form the sulfenylated products on the active methylene group, 1-benzylsulfonyl-1-phthalimido(succinimido)thiopolyfluoroalkan-2-ones. Decomposition of the latter leads to formation of 1-benzylsulfonyl-1-thioxopolyfluoroalkan-2-ones. These compounds easily undergo the hetero Diels-Alder reaction with electron-rich 1,3-dienes as dienophiles and with electron-rich olefins as hetero-1,3-dienes. Polyfluoroalkyl substituted derivatives of six-membered sulfur-containing heterocycles, 5,6-dihydro-2H-thiins and 2,3-dihydro-1,4-oxathiins, are obtained as a result of these reactions. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:175 / 181
页数:7
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