Simple sulfinate synthesis enables C-H trifluoromethylcyclopropanation.
Simple sulfinate synthesis enables C-H trifluoromethylcyclopropanation.
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DOI:
10.1002/anie.201406622
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发表时间:
2014-09-08
影响因子:
16.6
通讯作者:
Baran, Phil S.
中科院分区:
文献类型:
--
作者:
Gianatassio, Ryan;Kawamura, Shuhei;Eprile, Cecil L.;Foo, Klement;Ge, Jason;Burns, Aaron C.;Collins, Michael R.;Baran, Phil S.
A simple method to convert readily available carboxylic acids into sulfinate salts employing an interrupted Barton decarboxylation reaction is reported. A medicinally oriented panel of ten new sulfinate reagents was created using this method, including a key trifluoromethylcyclopropanation reagent TFCS-Na. The reactivity of six of these salts towards C–H functionalization was field-tested using several different classes of heterocycles.
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影响因子:
15
作者:
Fujiwara, Yuta;Dixon, Janice A.;Rodriguez, Rodrigo A.;Baxter, Ryan D.;Dixon, Darryl D.;Collins, Michael R.;Blackmond, Donna G.;Baran, Phil S.
通讯作者:
Baran, Phil S.
影响因子:
7.3
作者:
Alig, Leo;Alsenz, Jochern;Waldineier, Pius
通讯作者:
Waldineier, Pius
影响因子:
1.8
作者:
INGOLD, KU;LUSZTYK, J;WALTON, JC
通讯作者:
WALTON, JC
DOI:
10.1039/c39830000939
发表时间:
1983-01-01
影响因子:
--
作者:
BARTON, DHR;CRICH, D;MOTHERWELL, WB
通讯作者:
MOTHERWELL, WB
影响因子:
1.8
作者:
CASTAGNINO, E;CORSANO, S;ZARD, SZ
通讯作者:
ZARD, SZ