Gary M. Gallego, Ph.D.

Affiliations: 
2013 Chemistry University of California, Berkeley, Berkeley, CA, United States 
Area:
Total synthesis of biologically active natural products
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"Gary Gallego"
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Richmond Sarpong grad student 2013 UC Berkeley
 (Enantioselective hydroarylation of unactivated ketones with aryl pinacolboronic esters and a hydrindanone-based approach toward natural products.)
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Publications

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Burtea A, DeForest J, Baldwin N, et al. (2022) A convenient and versatile SAr-decarboxylation protocol for the construction of C(sp)-C(sp) bonds. Chemical Communications (Cambridge, England)
Kang T, Erbay TG, Xu KL, et al. (2020) Multifaceted Substrate-Ligand Interactions Promote the Copper-Catalyzed Hydroboration of Benzylidenecyclobutanes and Related Compounds. Acs Catalysis. 10: 13075-13083
Xiang J, Shang M, Kawamata Y, et al. (2019) Hindered dialkyl ether synthesis with electrogenerated carbocations. Nature
Ni S, Muñoz Padial N, Kingston C, et al. (2019) A Radical Approach to Anionic Chemistry: Synthesis of Ketones, Alcohols, and Amines. Journal of the American Chemical Society
Doering NA, Kou KGM, Norseeda K, et al. (2018) A Copper-Mediated Conjugate Addition Approach to Analogs of Aconitine-Type Diterpenoid Alkaloids. The Journal of Organic Chemistry
Merchant RR, Edwards JT, Qin T, et al. (2018) Modular radical cross-coupling with sulfones enables access to sp-rich (fluoro)alkylated scaffolds. Science (New York, N.Y.)
Kou KGM, Kulyk S, Marth CJ, et al. (2017) A Unifying Synthesis Approach to the C18‒, C19‒, and C20‒Diterpenoid Alkaloids. Journal of the American Chemical Society
Kou KG, Li BX, Lee JC, et al. (2016) Syntheses of Denudatine Diterpenoid Alkaloids: Cochle-arenine, N-Ethyl-1α-Hydroxy-17-Veratroyldictizine, and Paniculamine. Journal of the American Chemical Society
Gianatassio R, Lopchuk JM, Wang J, et al. (2016) Strain-release amination. Science (New York, N.Y.). 351: 241-246
Marth CJ, Gallego GM, Lee JC, et al. (2015) Network-analysis-guided synthesis of weisaconitine D and liljestrandinine. Nature
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