Gia L Hoang

Affiliations: 
Chemistry Yale University, New Haven, CT 
Area:
Organometallic, organic synthesis, catalysis
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"Gia Hoang"
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Streit AD, Zoll AJ, Hoang GL, et al. (2020) Annulation of Hydrazones and Alkynes via Rhodium(III)-Catalyzed Dual C-H Activation: Synthesis of Pyrrolopyridazines and Azolopyridazines. Organic Letters
Hoang GL, Zoll AJ, Ellman JA. (2019) Three-Component Coupling of Aldehydes, 2-Aminopyridines, and Diazo Esters via Rhodium(III)-Catalyzed Imidoyl C-H Activation: Synthesis of Pyrido[1,2- a]pyrimidin-4-ones. Organic Letters
Hoang GL, Streit AD, Ellman JA. (2018) Three-Component Coupling of Aldehydes, Aminopyrazoles, and Sulfoxonium Ylides via Rhodium(III)-Catalyzed Imidoyl C-H Activation: Synthesis of Pyrazolo[1,5- a]pyrimidines. The Journal of Organic Chemistry
Hoang GL, Ellman JA. (2018) Rhodium(III)-catalyzed C-H functionalization of C-alkenyl azoles with sulfoxonium ylides for the synthesis of bridgehead -fused [5,6]-bicyclic heterocycles. Tetrahedron. 74: 3318-3324
Hoang GL, Søholm Halskov K, Ellman JA. (2018) Synthesis of Azolo[1,3,5]triazines via Rhodium(III)-Catalyzed Annulation of N-Azolo Imines and Dioxazolones. The Journal of Organic Chemistry
Hoang GL, Zhang S, Takacs JM. (2018) Rhodium-catalyzed asymmetric hydroboration of γ,δ-unsaturated amide derivatives: δ-borylated amides. Chemical Communications (Cambridge, England)
Halskov KS, Witten MR, Hoang GL, et al. (2018) Rhodium(III)-Catalyzed Imidoyl C-H Activation for Annulations to Azolopyrimidines. Organic Letters
Hoang GL, Takacs JM. (2017) Enantioselective γ-borylation of unsaturated amides and stereoretentive Suzuki-Miyaura cross-coupling. Chemical Science. 8: 4511-4516
Hoang GL, Yang ZD, Smith SM, et al. (2015) Enantioselective desymmetrization via carbonyl-directed catalytic asymmetric hydroboration and Suzuki-Miyaura cross-coupling. Organic Letters. 17: 940-3
Yang ZD, Pal R, Hoang GL, et al. (2014) Mechanistic Insights into Carbonyl-Directed Rhodium-Catalyzed Hydroboration: ab Initio Study of a Cyclic γ,δ-Unsaturated Amide. Acs Catalysis. 4: 763-773
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