Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Christopher J. Lata"'
Publikováno v:
Angewandte Chemie. 119:7945-7948
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0eccf512b72fc0097e84302d71f90602
https://doi.org/10.1002/ange.200702563
https://doi.org/10.1002/ange.200702563
Autor:
Matthew P. Thompson, Cathleen M. Crudden, Robert P. Lemieux, Pedro J. Montoya-Pelaez, Yoon-Seo Uh, Christopher J. Lata
Publikováno v:
The Journal of Organic Chemistry. 71:5921-5929
Various routes were examined for the synthesis of chiral biphenyl species that are substituted at the 2,2', 4,4' and 6,6' positions. Because the biaryl bond is tetrasubstituted, many coupling reactions were not suitable. The most reliable coupling re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ac239d76f3f3883f4932f6ee494cea
https://doi.org/10.1021/jo060553d
https://doi.org/10.1021/jo060553d
Publikováno v:
ChemInform. 41
The addition of Lewis acids such as trispentafluoroboron as cocatalysts has been found to have a dramatic effect on the Rh-catalyzed hydroboration of olefins with pinacol borane. For example, aliphatic olefins do not react at all in noncoordinating s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4b654daec0f875ee6ad3570766666e4
https://doi.org/10.1002/chin.201028180
https://doi.org/10.1002/chin.201028180
Publikováno v:
Journal of the American Chemical Society. 132(1)
The addition of Lewis acids such as trispentafluoroboron as cocatalysts has been found to have a dramatic effect on the Rh-catalyzed hydroboration of olefins with pinacol borane. For example, aliphatic olefins do not react at all in noncoordinating s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30c48b27dd0679a65dcfa4a07e6a203d
https://pubmed.ncbi.nlm.nih.gov/19968306
https://pubmed.ncbi.nlm.nih.gov/19968306
Publikováno v:
Chemical communications (Cambridge, England). (44)
The use of boron chemistry for the synthesis of enantiomerically enriched organic compounds is described. Key advances towards the preparation of organoboranes with control of stereochemistry are supplemented by a discussion of the use of these chira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba812e91312b41f31e3a8410688548d3
https://pubmed.ncbi.nlm.nih.gov/19885455
https://pubmed.ncbi.nlm.nih.gov/19885455
Publikováno v:
Angewandte Chemie (International ed. in English). 46(41)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beef29de04a8de926e4a1c6993cd745b
https://pubmed.ncbi.nlm.nih.gov/17823901
https://pubmed.ncbi.nlm.nih.gov/17823901