Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Subhash D. Tanpure"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1008-1016 (2015)
Ammonium persulfate–dimethyl sulfoxide (APS–DMSO) has been developed as an efficient and new dehydrating reagent for a convenient one-pot process for the synthesis of miscellaneous cyclic imides in high yields starting from readily available prim
Externí odkaz:
https://doaj.org/article/8a5c8fcd76ee45f590e414b1e37d587d
Autor:
Paul R. Blakemore, Subhash D. Tanpure
Publikováno v:
European Journal of Organic Chemistry. 2021:4932-4937
Autor:
Darrin M. Flanigan, Subhash D. Tanpure, Tomislav Rovis, Alberto Muñoz, Paul R. Blakemore, Kerem Erol Ozboya
Publikováno v:
Organic Reactions. :1191-1330
Publikováno v:
Organic Letters. 22:2999-3003
To gauge the feasibility of carbenoid eliminative cross-coupling for the synthesis of polyfunctional alkenes, a P-glycoprotein inhibitor containing an (E)-configured 4-chromanylidene-type trisubsti...
Publikováno v:
Organic letters. 22(8)
To gauge the feasibility of carbenoid eliminative cross-coupling for the synthesis of polyfunctional alkenes, a P-glycoprotein inhibitor containing an (
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1008-1016 (2015)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
Ammonium persulfate–dimethyl sulfoxide (APS–DMSO) has been developed as an efficient and new dehydrating reagent for a convenient one-pot process for the synthesis of miscellaneous cyclic imides in high yields starting from readily available prim
Publikováno v:
RSC Advances. 5:101641-101646
Activation of DMSO to work as an economical and environmentally benign one-carbon synthon has been achieved by using a bench-top reagent ammonium persulfate for general and efficient access to symmetrical methylenebisamides from primary amides. This
Publikováno v:
ChemInform. 47
The Beckmann rearrangement of ketoximes, mediated by ammonium persulfate-dimethyl sulfoxide as a reagent, has been achieved under neutral conditions. Based on the radical trapping and 18O-labeling experiments, the transformation follows a mechanism i
Publikováno v:
Organic letters. 18(14)
The Beckmann rearrangement of ketoximes, mediated by ammonium persulfate-dimethyl sulfoxide as a reagent, has been achieved under neutral conditions. Based on the radical trapping and (18)O-labeling experiments, the transformation follows a mechanism
Publikováno v:
ChemInform. 47
Activation of DMSO to work as an economical and environmentally benign one-carbon synthon has been achieved by using a bench-top reagent ammonium persulfate for general and efficient access to symmetrical methylenebisamides from primary amides. This