Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Elena Braconi"'
Publikováno v:
Journal of the American Chemical Society. 142:19819-19824
Chiral cyclooctadienes are a frequently occurring scaffold in natural products and specialty chemicals, and are used as ligands in asymmetric catalysis. Accessing substituted cyclooctadienes in an efficient asymmetric fashion has been notoriously cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::122226a998f9e3feebc9e0989ef5a8b5
https://doi.org/10.1021/jacs.0c09486
https://doi.org/10.1021/jacs.0c09486
Autor:
Elena Braconi, Nicolai Cramer
Publikováno v:
Angewandte Chemie International Edition. 61
The cyclohexene motif is ubiquitous in nature and specialty chemicals. A straightforward selective access to chiral cyclohexenes from unactivated dienes and dienophiles is not feasible by classical Diels-Alder reaction and constitutes an unsolved syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc58e424e21003e6eae6c319a7a84845
https://doi.org/10.1002/anie.202112148
https://doi.org/10.1002/anie.202112148
Publikováno v:
Angewandte Chemie International Edition
Atropo-enantioselective C-H functionalization reactions are largely limited to the dynamic kinetic resolution of biaryl substrates through the introduction of steric bulk proximal to the axis of chirality. Reported herein is a highly atropo-enantiose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bf86cc9da60744bd9f2a81e376ed53c
https://pubmed.ncbi.nlm.nih.gov/29963763
https://pubmed.ncbi.nlm.nih.gov/29963763
Autor:
Elena Braconi, Nicolai Cramer
A novel class of chiral naphthyridine diimine ligands (NDI*) readily accessible from C2 -symmetric 2,6-di-(1-arylethyl)anilines is described. The utility of these ligands, particularly one with fluorinated aryl side arms, is demonstrated by a reducti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::277ea9cd2579e6fc93f77005aa71e6ed
https://infoscience.epfl.ch/record/280836
https://infoscience.epfl.ch/record/280836
