Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ganesh Kumar Thota"'
Publikováno v:
Advanced Synthesis & Catalysis. 360:1094-1098
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c7e6da19912bcfce30703e804fab621
https://doi.org/10.1002/adsc.201701377
https://doi.org/10.1002/adsc.201701377
Publikováno v:
European Journal of Organic Chemistry. 2017:6417-6426
Diastereoselective synthesis of highly substituted pyrrolidines has been accomplished with a six carbon building block bearing different reactive carbons. In this reaction the building block acts a 1,3-dipole and undergo cyclization with imines forme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::241bd2d4a6dedbfbcec3ebc00fcf66fa
https://doi.org/10.1002/ejoc.201700997
https://doi.org/10.1002/ejoc.201700997
Publikováno v:
Organic Chemistry Frontiers. 4:573-577
A catalytic enantioselective hydroxyamination of α,β-unsaturated 2-acyl imidazoles with N-protected hydroxyl amines catalyzed by a chiral-at-metal Rh(III) complex (0.5–2 mol%) has been developed. The approach affords valuable N-Boc protected β-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::082f648efc77dd3bb81fb4a7f62d4b93
https://doi.org/10.1039/c6qo00865h
https://doi.org/10.1039/c6qo00865h
Publikováno v:
European Journal of Organic Chemistry. 2016:5855-5861
Regioselective hydration of α-alkynyl esters and ketones by using a cationic NHC–AuI catalyst results in β-keto esters and β-diketones, respectively. Controlled release of water in acetone by aldol self-condensation under the reaction conditions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e037260aefb83ad3d3ff34ff08e3c34
https://doi.org/10.1002/ejoc.201601025
https://doi.org/10.1002/ejoc.201601025
Publikováno v:
Tetrahedron. 71:2280-2289
Generation of diol equivalent from epoxide under gold catalysis for the intermolecular reaction with terminal alkynes to generate 1,3-dioxolane has been achieved. Oxo- and alkynophilicities of gold catalyst play important role in tandem to effect thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::beb71b34e63e36568cc4710bc1e9b344
https://doi.org/10.1016/j.tet.2015.02.040
https://doi.org/10.1016/j.tet.2015.02.040
Publikováno v:
European Journal of Organic Chemistry. 2011:1557-1569
Gold-catalysed generation of diol equivalents from epoxides and their intramolecular reaction with C≡C bonds to generate bicyclic ketals is presented. This reaction essentially involves the formation of an acetonide, which subsequently cyclises on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ce517795339f9654dadb12879551f94
https://doi.org/10.1002/ejoc.201001214
https://doi.org/10.1002/ejoc.201001214