Ke Kong, Ph.D. - Publications
Affiliations: | Texas A & M University, College Station, TX, United States |
Area:
Natural Product Synthesis, Organic ChemistryYear | Citation | Score | |||
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2018 | Huang YW, Kong K, Wood J. Total Synthesis of (+)- and (±)-Hosieine A. Angewandte Chemie (International Ed. in English). PMID 29723446 DOI: 10.1002/Anie.201804076 | 0.331 | |||
2015 | Chen J, Chen Y, Wang X, Kong K, Cao W. Synthesis and characterization of oxadisilole-fused phenanthridines and dioxatrisilole-fused phenanthridines from benzyne Tetrahedron. 71: 5130-5136. DOI: 10.1016/j.tet.2015.05.064 | 0.329 | |||
2014 | Matsumaru T, McCallum ME, Enquist JA, Smith GM, Kong K, Wood JL. Synthetic studies toward the citrinadins: Enantioselective preparation of an advanced spirooxindole intermediate Tetrahedron. 70: 4089-4093. DOI: 10.1016/j.tet.2014.02.046 | 0.31 | |||
2013 | Kong K, Enquist JA, McCallum ME, Smith GM, Matsumaru T, Menhaji-Klotz E, Wood JL. An enantioselective total synthesis and stereochemical revision of (+)-citrinadin B. Journal of the American Chemical Society. 135: 10890-3. PMID 23837485 DOI: 10.1021/Ja405548B | 0.379 | |||
2011 | Kong K, Moussa Z, Lee C, Romo D. Total synthesis of the spirocyclic imine marine toxin (-)-gymnodimine and an unnatural C4-epimer. Journal of the American Chemical Society. 133: 19844-56. PMID 22023219 DOI: 10.1021/Ja207385Y | 0.557 | |||
2009 | Kong K, Romo D, Lee C. Enantioselective total synthesis of the marine toxin (-)-gymnodimine employing a Barbier-type macrocyclization. Angewandte Chemie (International Ed. in English). 48: 7402-5. PMID 19728353 DOI: 10.1002/Anie.200903432 | 0.46 | |||
2006 | Kong K, Romo D. Diastereoselective, vinylogous mukaiyama aldol additions of silyloxy furans to cyclic ketones: annulation of butenolides and gamma-lactones. Organic Letters. 8: 2909-12. PMID 16805514 DOI: 10.1021/Ol060534Q | 0.536 | |||
2005 | Kong K, Moussa Z, Romo D. Studies toward a marine toxin immunogen: enantioselective synthesis of the spirocyclic imine of (-)-gymnodimine. Organic Letters. 7: 5127-30. PMID 16268519 DOI: 10.1021/Ol051840R | 0.552 | |||
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