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pro vyhledávání: '"Carolyn E. Anderson"'
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 77, Iss 5, Pp 537-541 (2021)
The title ketenylidene, [Au3(C2O)(C26H35O2P)3](C2F6NO4S2), was obtained upon exposure of [2-(dicyclohexylphosphino)-2′,6′-dimethoxy-1,1′-biphenyl]gold(I) bis(trifluoromethanesulfonyl)imide to acetic anhydride at elevated temperature. The keteny
Externí odkaz:
https://doaj.org/article/98ff977d21d5417c919b78376213be95
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications
Acta Crystallographica Section E: Crystallographic Communications, Vol 77, Iss 5, Pp 537-541 (2021)
Acta Crystallographica Section E: Crystallographic Communications, Vol 77, Iss 5, Pp 537-541 (2021)
The title compound contains a ketenylidene bridge that caps a tri-gold cluster. This is the first reported tri-gold ketenylidene with atomic distances indicative of bonding interaction between the gold atoms.
The title ketenylidene, [Au3
The title ketenylidene, [Au3
Autor:
Connor P. Reidy, Evan O. Romero, Nicholas W. Vryhof, Andrea N. Bootsma, David C. Wierenga, Carolyn E. Anderson, Noah M. PreFontaine
Publikováno v:
The Journal of Organic Chemistry. 85:3990-3991
Autor:
Leslie A. Nickerson, Evan O. Romero, Jaimie E. Van de Burg, Colin T. Hartgerink, Emily E. Zerull, Matthew D. Rossler, Richard J. Staples, Miles M. Mason, Abigail K. Frndak, Carolyn E. Anderson, Benjamin L. Boss
Publikováno v:
Organic letters. 21(14)
A new Au(I)-catalyzed method for the preparation of trisubstituted indolizines from easily accessible 2-propargyloxy-pyridines is reported. The reaction tolerates a wide range of functionality, allowing for diversity to be introduced in four distinct
Autor:
Noah M. PreFontaine, Evan O. Romero, Nicholas W. Vryhof, Connor P. Reidy, David C. Wierenga, Andrea N. Bootsma, Carolyn E. Anderson
Publikováno v:
The Journal of Organic Chemistry. 81:9895-9902
N-Alkyl 2-pyridones and other enolizable heterocycles are important synthetic constructs, due to their prevalence in natural products and pharmaceutical targets and their capacity to serve as models for a number of biological and chemical processes.
Autor:
Carolyn E. Anderson, Jackson L. Ross, David E. Benson, Elysa M. Wolf, Andrew G. Roth, Taylor R. Hegg, Susan E. Hromada, Adam M. Hilbrands, Matthew T. Hollowell
Publikováno v:
Journal of inorganic biochemistry. 176
Some post-translationally modified tyrosines can perform reversible redox chemistry similar to metal cofactors. The most studied of these tyrosine modifications is the intramolecular thioether-crosslinked 3'-(S-cysteinyl)-tyrosine (Cys-Tyr) in galact
Autor:
Keun Ah Ryu, Christina A. Shandro, Sarah Z. Tasker, Bruce A. Ellsworth, Erica L. Lanni, Jarrad M. Utter, Gregory S. Snapper, Carolyn E. Anderson, Michael A. Bosscher
Publikováno v:
The Journal of Organic Chemistry. 77:8220-8230
An efficient and inexpensive LiI-promoted O- to N-alkyl migration of 2-benzyloxy-, 2-allyloxy-, and 2-propargyloxypyridines and heterocycles is reported. The reaction produces the corresponding N-alkyl 2-pyridones and analogues under green, solvent-f
Publikováno v:
Organic Letters. 14:874-877
A new Au(III)-catalyzed tandem amination-hydration reaction has been discovered, leading to the formation of α-(N-2-pyridonyl)ketones and heterocyclic analogues in good to excellent yields (14 examples, 48-90%). This reaction demonstrates the unusua
Autor:
Carolyn E. Anderson, Sarah Z. Tasker, Richard J. Staples, Roger L. DeKock, Benjamin M. Brandsen, Keun Ah Ryu, Gregory S. Snapper
Publikováno v:
Organic Letters. 13:6224-6227
A new method for the synthesis of β-iodo N-alkenyl 2-pyridones from substituted 2-propargyloxypyridines has been discovered . These compounds present a unique complement of orthogonal functionality and structural characteristics that are unavailable
Autor:
Carolyn E. Anderson, Bruce A. Ellsworth, Michael A. Bosscher, Erica L. Lanni, Christina A. Shandro, Bartel D. Ooms
Publikováno v:
The Journal of Organic Chemistry. 73:6425-6428
A new LiI-promoted O- to N-alkyl migration has been developed for the conversion of O-alkylated 2-hydroxy pyridines, quinolines, and pyrimidines to the corresponding N-alkylated heterocycles in good to excellent yields (57-99%). This method serves as