Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jesse B. Kidd"'
Publikováno v:
Chem Rev
Asymmetric catalysis is a major theme of research in contemporary synthetic organic chemistry. The discovery of general strategies for highly enantioselective photochemical reactions, however, has been a relatively recent development, and the variety
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d142f0a99bb0685401bf5e56982c34c8
https://pubmed.ncbi.nlm.nih.gov/34606251
https://pubmed.ncbi.nlm.nih.gov/34606251
Publikováno v:
Journal of the American Chemical Society. 139:17186-17192
Stereochemical control of electronically excited states is a long-standing challenge in photochemical synthesis, and few catalytic systems that produce high enantioselectivities in triplet-state photoreactions are known. We report herein an exception
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d43a32cb96b08006fd881958d644f5a3
https://doi.org/10.1021/jacs.7b10586
https://doi.org/10.1021/jacs.7b10586
Autor:
Jian Zheng, Kazimer L. Skubi, Gerald J. Meyer, Jesse B. Kidd, Hoimin Jung, Tehshik P. Yoon, Wesley B. Swords, Mu-Hyun Baik
Publikováno v:
J Am Chem Soc
Enantioselective catalysis of excited-state photoreactions remains a substantial challenge in synthetic chemistry, and intermolecular photoreactions have proven especially difficult to conduct in a stereocontrolled fashion. Herein, we report a highly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ac18ebc890fb75cd6345e36704990ec
https://pubmed.ncbi.nlm.nih.gov/31329459
https://pubmed.ncbi.nlm.nih.gov/31329459
Publikováno v:
ChemInform. 47
Functionalized tryptamines are targets of interest for development as small molecule therapeutics. The ring opening of aziridines with indoles is a powerful method for tryptamine synthesis if site selectivity can be controlled. 4-Nitrobenzyl carbamat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d5a3501dc03be60be08abcbfc323836
https://doi.org/10.1002/chin.201641137
https://doi.org/10.1002/chin.201641137
Publikováno v:
Tetrahedron. 72(26)
Functionalized tryptamines are targets of interest for development as small molecule therapeutics. The ring opening of aziridines with indoles is a powerful method for tryptamine synthesis if site selectivity can be controlled. 4-Nitrobenzyl carbamat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::747cff2d082e5bf713fbc182fb08363a
https://pubmed.ncbi.nlm.nih.gov/27378819
https://pubmed.ncbi.nlm.nih.gov/27378819