Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Joseph J. Badillo"'
Publikováno v:
Organic & Biomolecular Chemistry. 20:6188-6192
In this report, we demonstrate that visible light photoactivation of 6-bromo-2-naphthol facilitates the photoacid-catalyzed acetalization of carbonyls with alcohols. We also demonstrate that 2-naphthol when coupled to a photosensitizer provides aceta
Publikováno v:
Synthesis. 53:489-497
Photoacids are molecules that become more acidic upon the absorption of light. This short review highlights recent advances in the use of photoacids as catalysts for organic synthesis. Photoacid-catalyzed transformations discussed herein include: P
Publikováno v:
Organic letters. 21(21)
In this report, we demonstrate that visible-light-induced thiourea photoacids catalyze C–C bond-forming reactions. Upon photoirradiation, Schreiner’s thiourea [(N,N′-bis[3,5-bis(trifluoromethyl)phe...
Publikováno v:
ChemInform. 46
The presented stereoselective [3+2] cycloaddition affords the title spiro compounds in excellent yields and good diastereoselectivities.
Publikováno v:
ChemInform. 46
The first catalytic asymmetric [3 + 2] annulation of 3-methylene substituted oxindoles with allylsilanes is developed to give spirocyclopentane derivatives in high diastereo- and enantioselectivity.
Publikováno v:
Angewandte Chemie (International ed. in English), vol 53, iss 36
The first catalytic asymmetric carboannulation with allylsilanes is presented. The enantioselective [3+2] annulation is catalyzed using a scandium(III)/indapybox complex with tetrakis-[3,5-bis(trifluoromethyl)phenyl]-borate (BArF) to enhance catalyti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0de7d955509a2f7ca6e316145398ad33
https://escholarship.org/uc/item/9k2684mb
https://escholarship.org/uc/item/9k2684mb
Publikováno v:
ChemInform. 43
Oxindoles and spirooxindoles are important synthetic targets that are often considered to be prevalidated with respect to their biological activity and applications for pharmaceutical lead discovery. This review features efficient strategies for the
Publikováno v:
Organicbiomolecular chemistry. 10(27)
Oxindoles and spirooxindoles are important synthetic targets that are often considered to be prevalidated with respect to their biological activity and applications for pharmaceutical lead discovery. This review features efficient strategies for the
Autor:
Gary E. Arevalo, Jacob P. MacDonald, Annaliese K. Franz, Abel Silva-García, Joseph J. Badillo
Publikováno v:
ACS Combinatorial Science
A strategy for the efficient two-step synthesis of triazole derivatives of oxindoles and spirooxindoles is presented. Using a common set of N-propargylated isatins, a series of mechanistically distinct stereoselective reactions with different combina
Autor:
Benjamin H. Shupe, Joseph J. Badillo, James C. Fettinger, Abel Silva-García, Annaliese K. Franz
Publikováno v:
ChemInform. 43
Among various BINOL-derived phosphoric acids, derivatives (Ia) and (Ib) are found to be the most efficient ones.