Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tabitha T. Schempp"'
Autor:
Tabitha T. Schempp, Michael J. Krische
Publikováno v:
J Am Chem Soc
The total synthesis of soraphen A, a myxobacterial metabolite and inhibitor of acetyl CoA carboxylase, was completed in 11 steps (longest linear sequence), less than half the steps previously required. Seven metal-catalyzed processes were deployed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::577684b24e85e0245035ad94ee61e36b
https://europepmc.org/articles/PMC8852841/
https://europepmc.org/articles/PMC8852841/
Publikováno v:
Organic Letters. 19:3616-3619
The preparation of substituted azaindolines utilizing a domino palladium-catalyzed Heck cyclization/Suzuki coupling is described. The approach is amenable for the construction of all four azaindoline isomers. A range of functional groups such as este
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::818a9e8ed295ea1ddee57e39c4ac23fa
https://doi.org/10.1021/acs.orglett.7b01606
https://doi.org/10.1021/acs.orglett.7b01606
Autor:
Robert A. Swyka, William G. Shuler, Michael J. Krische, Tabitha T. Schempp, Brian J. Spinello
Publikováno v:
Chemistry
Direct conversion of aldehydes to ketones is achieved via rhodium-catalyzed vinyl triflate-aldehyde reductive coupling-redox isomerization mediated by potassium formate. This method circumvents premetalated C-nucleophiles and discrete redox manipulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff8a290751ad86aba4c653ea6ead001e
https://pubmed.ncbi.nlm.nih.gov/31403727
https://pubmed.ncbi.nlm.nih.gov/31403727
Publikováno v:
Angew Chem Int Ed Engl
Rough, Ready and Regioselective. Stable to air, water and SiO(2), cyclometallated π-allyliridium C,O-benzoates modified by (S)-tol-BINAP catalyze highly enantioselective N-allylations of indoles and related azoles. Complementing the scope of all pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4160ef88873e85abcb0713c7fbe9f56
https://pubmed.ncbi.nlm.nih.gov/30964961
https://pubmed.ncbi.nlm.nih.gov/30964961
Autor:
Liang X; University of Texas at Austin, Department of Chemistry, 105 E 24th St. (A5300), Austin, TX 78712-1167, USA., Yoo M; University of Texas at Austin, Department of Chemistry, 105 E 24th St. (A5300), Austin, TX 78712-1167, USA., Schempp T; University of Texas at Austin, Department of Chemistry, 105 E 24th St. (A5300), Austin, TX 78712-1167, USA., Maejima S; University of Texas at Austin, Department of Chemistry, 105 E 24th St. (A5300), Austin, TX 78712-1167, USA., Krische MJ; University of Texas at Austin, Department of Chemistry, 105 E 24th St. (A5300), Austin, TX 78712-1167, USA.
Publikováno v:
Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2022 Dec 23; Vol. 61 (52), pp. e202214786. Date of Electronic Publication: 2022 Nov 23.