Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Michael Callingham"'
Autor:
Stephen P. Argent, Jinwei Sun, Alistair Groves, Laurence J. Taylor, Michael Callingham, Hal R. I. Parke, Hon Wai Lam
Publikováno v:
Chemical Science
The enantioselective synthesis of densely functionalized polycarbocycles by the rhodium(i)-catalyzed reaction of arylboronic acids with 1,3-diketones is described. The key step in these desymmetrizing domino addition–cyclization reactions is an alk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d3cd0fc81cc6dde7f519cad9c4f2b22
http://europepmc.org/articles/PMC8157494
http://europepmc.org/articles/PMC8157494
Publikováno v:
Chemical Communications. 55:838-841
A novel multicomponent coupling reaction involving the iridium-catalyzed 1,5-difunctionalization of 1,3-enynes with arylboronic acids and triazinanes is described. A key step in this 1,5-(aryl)aminomethylation reaction is the alkenyl-to-allyl 1,4-iri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eed5e098e1f75a571b3c559cf0e68e20
https://doi.org/10.1039/c8cc09238a
https://doi.org/10.1039/c8cc09238a
Publikováno v:
Angewandte Chemie (International Ed. in English)
A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3‐enynes, and imines to give homoallylic sulfamates. The key step is the generation of allylrhodium(I) species by alkenyl‐to‐allyl 1,4‐rhodium(I)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f62a9805bd9985617c5fc04bc56f986f
https://doi.org/10.1002/anie.201709334
https://doi.org/10.1002/anie.201709334
Publikováno v:
Angewandte Chemie. 129:7333-7338
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36f9d6ef5e9a3d0784c04e8c273d5f67
https://doi.org/10.1002/ange.201703155
https://doi.org/10.1002/ange.201703155
A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3-enynes, and imines to give homoallylic sulfamates. The key step is the generation of allylrhodium(I) species by alkenyl-to-allyl 1,4-rhodium(I) migratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::035cd404d81453f72a6d6f5339464117
https://nottingham-repository.worktribe.com/file/900327/1/Callingham_et_al-2017-Angewandte_Chemie_International_Edition.pdf
https://nottingham-repository.worktribe.com/file/900327/1/Callingham_et_al-2017-Angewandte_Chemie_International_Edition.pdf
Publikováno v:
ChemInform. 47
A novel, high-yielding, one-step synthesis of 2-chloroquinazolin-4-ols and analogous bicycles from 2-aminoamides using thiophosgene is described. The scope of the reaction includes aminothioamides, amino acids, and fused heterocycle derivatives, furn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f31f71dd8a0da4f7bdae2b840b5b464
https://doi.org/10.1002/chin.201608185
https://doi.org/10.1002/chin.201608185
Publikováno v:
Organic letters. 17(19)
A novel, high-yielding, one-step synthesis of 2-chloroquinazolin-4-ols and analogous bicycles from 2-aminoamides using thiophosgene is described. The scope of the reaction includes aminothioamides, amino acids, and fused heterocycle derivatives, furn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35ac35330469e26bc2b05dc41c9ac7e4
https://pubmed.ncbi.nlm.nih.gov/26360817
https://pubmed.ncbi.nlm.nih.gov/26360817
Publikováno v:
Organic Letters; Oct2015, Vol. 17 Issue 19, p4930-4932, 3p