Colin K. Skepper, Ph.D. - Publications

Affiliations: 
2009 Chemistry University of California, San Diego, La Jolla, CA 
Area:
Organic chemistry of marine natural products, synthesis, NMR, and biomedical applications

13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Skepper CK, Molinski TF. Synchronous bond molecular dynamics of conjugated chlorocyclopropyl alk-yn-enes revealed by ECD and UV-vis. Chirality. PMID 32567115 DOI: 10.1002/chir.23240  0.527
2017 Yang S, Sankar K, Skepper CK, Barker TJ, Lukesh JC, Brody DM, Brütsch MM, Boger DL. Total synthesis of a key series of vinblastines modified at C4 that define the importance and surprising trends in activity. Chemical Science. 8: 1560-1569. PMID 28194270 DOI: 10.1039/C6Sc04146A  0.396
2013 Campbell EL, Skepper CK, Sankar K, Duncan KK, Boger DL. Transannular Diels-Alder/1,3-dipolar cycloaddition cascade of 1,3,4-oxadiazoles: total synthesis of a unique set of vinblastine analogues. Organic Letters. 15: 5306-9. PMID 24087969 DOI: 10.1021/Ol402549N  0.41
2010 Skepper CK, Quach T, Molinski TF. Total synthesis of enigmazole A from Cinachyrella enigmatica. Bidirectional bond constructions with an ambident 2,4-disubstituted oxazole synthon. Journal of the American Chemical Society. 132: 10286-92. PMID 20590095 DOI: 10.1021/Ja1016975  0.566
2010 Skepper CK, Dalisay DS, Molinski TF. Synthesis and chain-dependent antifungal activity of long-chain 2H-azirine-carboxylate esters related to dysidazirine. Bioorganic & Medicinal Chemistry Letters. 20: 2029-32. PMID 20171099 DOI: 10.1016/J.Bmcl.2010.01.068  0.547
2009 Dalisay DS, Morinaka BI, Skepper CK, Molinski TF. A tetrachloro polyketide hexahydro-1H-isoindolone, muironolide A, from the marine sponge Phorbas sp. natural products at the nanomole scale. Journal of the American Chemical Society. 131: 7552-3. PMID 19453148 DOI: 10.1021/Ja9024929  0.723
2008 Skepper CK, Dalisay DS, Molinski TF. Synthesis and antifungal activity of (-)-(Z)-dysidazirine. Organic Letters. 10: 5269-71. PMID 18937483 DOI: 10.1021/Ol802065D  0.569
2008 MacMillan JB, Xiong-Zhou G, Skepper CK, Molinski TF. Phorbasides A-E, cytotoxic chlorocyclopropane macrolide glycosides from the marine sponge Phorbas sp. CD determination of C-methyl sugar configurations. The Journal of Organic Chemistry. 73: 3699-706. PMID 18412387 DOI: 10.1021/Jo702307T  0.697
2008 Skepper CK, Molinski TF. Long-chain 2H-azirines with heterogeneous terminal halogenation from the marine sponge Dysidea fragilis. The Journal of Organic Chemistry. 73: 2592-7. PMID 18321120 DOI: 10.1021/Jo702435S  0.568
2007 Makarieva TN, Dmitrenok PS, Zakharenko AM, Denisenko VA, Guzii AG, Li R, Skepper CK, Molinski TF, Stonik VA. Rhizochalins C and D from the sponge Rhizochalina incrustata. A rare threo-sphingolipid and a facile method for determination of the carbonyl position in alpha,omega-bifunctionalized ketosphingolipids. Journal of Natural Products. 70: 1991-8. PMID 18052325 DOI: 10.1021/Np0704811  0.532
2007 Morinaka BI, Skepper CK, Molinski TF. Ene-yne tetrahydrofurans from the sponge Xestospongia muta. exploiting a weak CD effect for assignment of configuration. Organic Letters. 9: 1975-8. PMID 17439137 DOI: 10.1021/Ol0705696  0.713
2007 Skepper CK, Macmillan JB, Zhou GX, Masuno MN, Molinski TF. Chlorocyclopropane macrolides from the marine sponge Phorbas sp. assignment of the configurations of phorbasides A and B by quantitative CD. Journal of the American Chemical Society. 129: 4150-1. PMID 17373800 DOI: 10.1021/Ja0703978  0.641
2005 Masuno MN, Young DM, Hoepker AC, Skepper CK, Molinski TF. Addition of Cl2C: to (-)-O-menthyl acrylate under sonication-phase-transfer catalysis. Efficient synthesis of (+)- and (-)-(2-chlorocyclopropyl)methanol. The Journal of Organic Chemistry. 70: 4162-5. PMID 15876110 DOI: 10.1021/Jo0480186  0.649
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