Zobrazeno 1 - 5
of 5
pro vyhledávání: '"James H, Herbort"'
Autor:
Stanley M. Jing, Vinayak Vishnu Pagar, Mahesh M. Parsutkar, Souvagya Biswas, T. V. RajanBabu, James H. Herbort
Publikováno v:
Acc Chem Res
ConspectusOne of the major challenges facing organic synthesis in the 21st century is the utilization of abundantly available feedstock chemicals for fine chemical synthesis. Regio- and enantioselective union of easily accessible 1,3-dienes and other
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3cb6d94291c33c9635096cacc583434
https://doi.org/10.1021/acs.accounts.1c00573
https://doi.org/10.1021/acs.accounts.1c00573
Publikováno v:
ACS Catalysis. 11:9605-9617
Two intermolecular hydroalkenylation reactions of 1,6-enynes are presented which yield substituted 5-membered carbo- and -heterocycles. This reactivity is enabled by a cationic bis-diphenylphosphinopropane (DPPP)CoI species which forms a cobaltacyclo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78d1104790c7754dc1876f06fd9bdc26
https://doi.org/10.1021/acscatal.1c02530
https://doi.org/10.1021/acscatal.1c02530
Publikováno v:
ACS catalysis. 11(15)
Two intermolecular hydroalkenylation reactions of 1,6-enynes are presented which yield substituted 5-membered carbo- and -heterocycles. This reactivity is enabled by a cationic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9501a4b5034ac389b68ca297310ef6e1
https://pubmed.ncbi.nlm.nih.gov/34745711
https://pubmed.ncbi.nlm.nih.gov/34745711
Autor:
Kohki M. Nakafuku, Ethan A. Wappes, Darsheed N. Mustafa, David A. Nagib, Andrew D. Chen, James H. Herbort
Publikováno v:
Chemical Science. 11:2479-2486
A radical cascade strategy for the modular synthesis of five-membered heteroarenes (e.g. oxazoles, imidazoles) from feedstock reagents (e.g. alcohols, amines, nitriles) has been developed. This double C–H oxidation is enabled by in situ generated i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c40a5b7b0481a8cbc2cabc8fa8dc44c
https://doi.org/10.1039/c9sc06239d
https://doi.org/10.1039/c9sc06239d
Autor:
Andrew D, Chen, James H, Herbort, Ethan A, Wappes, Kohki M, Nakafuku, Darsheed N, Mustafa, David A, Nagib
Publikováno v:
Chemical Science
A radical cascade strategy for the modular synthesis of five-membered heteroarenes (e.g. oxazoles, imidazoles) from feedstock reagents (e.g. alcohols, amines, nitriles) has been developed. This double C–H oxidation is enabled by in situ generated i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::56f78776b20f21cb0c4934f826f2c697
https://pubmed.ncbi.nlm.nih.gov/34084413
https://pubmed.ncbi.nlm.nih.gov/34084413