Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Alexander R. Abela"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 1040-1064 (2016)
Cationic palladium(II) complexes have been found to be highly reactive towards aromatic C–H activation of arylureas at room temperature. A commercially available catalyst [Pd(MeCN)4](BF4)2 or a nitrile-free cationic palladium(II) complex generated
Externí odkaz:
https://doaj.org/article/2e3539d08dbd431083e70a9a8cbe76d4
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 1040-1064 (2016)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
Cationic palladium(II) complexes have been found to be highly reactive towards aromatic C–H activation of arylureas at room temperature. A commercially available catalyst [Pd(MeCN)4](BF4)2 or a nitrile-free cationic palladium(II) complex generated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2845f8821f6928db14f50da21abc6c5b
https://doi.org/10.3762/bjoc.12.99
https://doi.org/10.3762/bjoc.12.99
Publikováno v:
Journal of the American Chemical Society. 139(20)
Herein we describe concise enantioselective chemical syntheses of (−)-viridin and (−)-viridiol. Our convergent approach couples two achiral fragments of similar complexity and employs an enantioselective intramolecular Heck reaction to set the ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85837411bccac8fedaa6dc8c0fc42673
https://pubmed.ncbi.nlm.nih.gov/28463562
https://pubmed.ncbi.nlm.nih.gov/28463562
Publikováno v:
ChemInform. 47
Cationic palladium(II) complexes have been found to be highly reactive towards aromatic C-H activation of arylureas at room temperature. A commercially available catalyst [Pd(MeCN)4](BF4)2 or a nitrile-free cationic palladium(II) complex generated in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ba861e154a85e4fff45cce843903258
https://doi.org/10.1002/chin.201631105
https://doi.org/10.1002/chin.201631105
Autor:
Subir Ghorai, Arkady Krasovskiy, Benjamin R. Taft, Bruce H. Lipshutz, Alexander R. Abela, Christophe Duplais
Publikováno v:
Platinum Metals Review. 56:62-74
Palladium-catalysed cross-couplings, in particular Heck, Suzuki-Miyaura and Negishi reactions developed over three decades ago, are routinely carried out in organic solvents. However, alternative media are currently of considerable interest given an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5a00ed0bb46f946b11a11c329159551
https://doi.org/10.1595/147106712x629761
https://doi.org/10.1595/147106712x629761
Autor:
Arkady Krasovskiy, Bruce H. Lipshutz, Alexander R. Abela, Takashi Nishikata, Žarko V. Bošković, Christophe Duplais
Publikováno v:
Lipshutz, Bruce H.; Abela, Alexander R.; Bošković, Žarko V.; Nishikata, Takashi; Duplais, Christophe; & Krasovskiy, Arkady. (2010). “Greening Up” Cross-Coupling Chemistry. Topics in Catalysis, 53(15), pp 985-990. doi: 10.1007/s11244-010-9537-1. Retrieved from: http://www.escholarship.org/uc/item/0ts1v52w
New methodologies that enable palladium catalyzed cross-coupling reactions to be performed under environmentally benign conditions (in water and/or at room temperature) have been developed. Described approaches involve in situ activation of carbon–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d668e2037cc9d012a9497a447e752fe6
https://doi.org/10.1007/s11244-010-9537-1
https://doi.org/10.1007/s11244-010-9537-1
Publikováno v:
Angewandte Chemie International Edition. 49:781-784
Palladium-catalyzed cross-coupling reactions of aryl halides with aromatic C–H bonds have emerged as a powerful method for the preparation of biaryls.[1,2] Despite substantially increased attention to the field, typical reaction conditions still re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcd680c814347aa4c3c725a5eac0d2ae
https://doi.org/10.1002/anie.200905967
https://doi.org/10.1002/anie.200905967
Publikováno v:
Angewandte Chemie. 122:793-796
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::689733e533f8cf62161a5b2719bdd8a1
https://doi.org/10.1002/ange.200905967
https://doi.org/10.1002/ange.200905967
Autor:
Bruce H, Lipshutz, Benjamin R, Taft, Alexander R, Abela, Subir, Ghorai, Arkady, Krasovskiy, Christophe, Duplais
Publikováno v:
Platinum metals review. 56(2)
Palladium-catalysed cross-couplings, in particular Heck, Suzuki-Miyaura and Negishi reactions developed over three decades ago, are routinely carried out in organic solvents. However, alternative media are currently of considerable interest given an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4148d2ce39eea2e56b5851ad5e9143ce
https://pubmed.ncbi.nlm.nih.gov/23555153
https://pubmed.ncbi.nlm.nih.gov/23555153
Autor:
Arkady Krasovskiy, Subir Ghorai, Bruce H. Lipshutz, Ralph Moser, Alexander R. Abela, Robert C. Gadwood, Christophe Duplais, Ricky D. Gaston, Takashi Nishikata
Publikováno v:
The Journal of organic chemistry. 76(11)
An environmentally benign surfactant (TPGS-750-M), a diester composed of racemic α-tocopherol, MPEG-750, and succinic acid, has been designed and readily prepared as an effective nanomicelle-forming species for general use in metal-catalyzed cross-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168ee0303419ed7f046fba5800615063
https://pubmed.ncbi.nlm.nih.gov/21548658
https://pubmed.ncbi.nlm.nih.gov/21548658