Changhong Ko, Ph.D.
Affiliations: | 2008 | University of Wisconsin, Madison, Madison, WI |
Area:
Natural Product SynthesisGoogle:
"Changhong Ko"Mean distance: 8.46 | S | N | B | C | P |
Parents
Sign in to add mentorRichard P. Hsung | grad student | 2008 | UW Madison | |
(Synthesis methods using cyclic acetals and aminals.) |
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Publications
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Madhusudhan Reddy G, Ko CT, Hsieh KH, et al. (2016) Expanding the scope of primary amine catalysis: Stereoselective synthesis of indanedione-fused 2,6-disubstituted trans-spirocyclohexanones. The Journal of Organic Chemistry |
Deng J, Hsung RP, Ko C. (2012) Gassman's cationic [2 + 2] cycloadditions using temporary tethers. Organic Letters. 14: 5562-5 |
Tang Y, Yang JH, Liu J, et al. (2012) Assembly of the southern macrocyclic half of (+)-spirastrellolide a through cyclic acetal tethered ring-closing metathesis and 1,3-anti-mukaiyama-aldol Heterocycles. 86: 565-598 |
Feltenberger JB, Ko C, Deng J, et al. (2012) Development of an intramolecular gassman's [2 + 2] cycloaddition Heterocycles. 84: 843-878 |
Ko C, Feltenberger JB, Ghosh SK, et al. (2008) Gassman's intramolecular [2 + 2] cationic cycloaddition. formal total syntheses of raikovenal and epi-raikovenal. Organic Letters. 10: 1971-4 |
Ko C, Hsung RP, Al-Rashid ZF, et al. (2007) A stereoselective intramolecular halo-etherification of chiral enamides in the synthesis of halogenated cyclic ethers. Organic Letters. 9: 4459-62 |
Song Z, Lu T, Hsung RP, et al. (2007) StereoselectiveSimmons-Smith cyclopropanation of chiral enamides. Angewandte Chemie (International Ed. in English). 46: 4069-72 |
Ko C, Hsung RP. (2007) An unusual stereoselectivity in the anomeric substitution with carbamates promoted by HNTf2. Organic & Biomolecular Chemistry. 5: 431-4 |
Ghosh SK, Ko C, Liu J, et al. (2007) A Ketal-Tethered RCM Strategy Toward the Synthesis of Spiroketal Related Natural Products. Cheminform. 38 |
Liu J, Yang JH, Ko C, et al. (2006) Synthesis of the C1-C16 fragment of spirastrellolide A Tetrahedron Letters. 47: 6121-6123 |