Year |
Citation |
Score |
2017 |
Zhang W, Chen C, He M, Zhu Z, Hogan P, Gilicky O, Dunwoody N, Ronn M. Process Research and Development of TP-808: A Key Intermediate for the Manufacture of Synthetic Tetracyclines Organic Process Research & Development. 21: 377-386. DOI: 10.1021/Acs.Oprd.7B00003 |
0.316 |
|
2016 |
Zhang W, Sun C, Hunt D, He M, Deng Y, Zhu Z, Chen C, Katz CE, Niu J, Hogan PC, Xiao X, Dunwoody N, Ronn M. Process Development and Scale-up of Fully Synthetic Tetracycline TP-2758: A Potent Antibacterial Agent with Excellent Oral Bioavailability Organic Process Research & Development. 20: 284-296. DOI: 10.1021/Acs.Oprd.5B00404 |
0.344 |
|
2015 |
Zhang WY, Hogan PC, Chen CL, Niu J, Wang Z, Lafrance D, Gilicky O, Dunwoody N, Ronn M. Process Research and Development of an Enantiomerically Enriched Allyic Amine, One of the Key Intermediates for the Manufacture of Synthetic Tetracyclines Organic Process Research and Development. 19: 1784-1795. DOI: 10.1021/Acs.Oprd.5B00274 |
0.388 |
|
2013 |
Clark RB, He M, Deng Y, Sun C, Chen CL, Hunt DK, O'Brien WJ, Fyfe C, Grossman TH, Sutcliffe JA, Achorn C, Hogan PC, Katz CE, Niu J, Zhang WY, et al. Synthesis and biological evaluation of 8-aminomethyltetracycline derivatives as novel antibacterial agents. Journal of Medicinal Chemistry. 56: 8112-38. PMID 24047201 DOI: 10.1021/Jm401211T |
0.308 |
|
2013 |
Ronn M, Zhu Z, Hogan PC, Zhang WY, Niu J, Katz CE, Dunwoody N, Gilicky O, Deng Y, Hunt DK, He M, Chen CL, Sun C, Clark RB, Xiao XY. Process R&D of eravacycline: The first fully synthetic fluorocycline in clinical development Organic Process Research and Development. 17: 838-845. DOI: 10.1021/Op4000219 |
0.384 |
|
2010 |
Jackson KL, Li W, Chen CL, Kishi Y. Scalable and efficient synthesis of the mycolactone core. Tetrahedron. 66: 2263-2272. PMID 20228884 DOI: 10.1016/J.Tet.2010.02.010 |
0.426 |
|
2010 |
Huang X-, Chen C, Lee G-, Peng S-. Enantioselective Allylation of Ketones Using a SpirocyclicChiral Borate Synfacts. 2010: 327-327. DOI: 10.1055/S-0029-1219334 |
0.432 |
|
2009 |
Chen CL, Namba K, Kishi Y. Attempts to improve the overall stereoselectivity of the Ireland-Claisen rearrangement. Organic Letters. 11: 409-12. PMID 19128191 DOI: 10.1021/Ol8027225 |
0.333 |
|
2007 |
Sparks SM, Chen CL, Martin SF. Tandem Intramolecular Benzyne-Furan Cycloadditions. Total Synthesis of Vineomycinone B(2) Methyl Ester. Tetrahedron. 63: 8619-8635. PMID 18728697 DOI: 10.1016/J.Tet.2007.04.031 |
0.684 |
|
2007 |
Martin S, Chen C, Sparks S. Synthesis of Vineomycinone B2 Methyl Ester Synfacts. 2007: 0236-0236. DOI: 10.1055/S-2007-968187 |
0.669 |
|
2006 |
Chen CL, Sparks SM, Martin SF. C-Aryl glycosides via tandem intramolecular benzyne-furan cycloadditions. Total synthesis of vineomycinone B2 methyl ester. Journal of the American Chemical Society. 128: 13696-7. PMID 17044691 DOI: 10.1021/Ja0652619 |
0.692 |
|
2006 |
Chen CL, Martin SF. Pd-catalyzed ring opening of oxa- and azabicyclic alkenes with aryl and vinyl halides: efficient entry to 2-substituted 1,2-dihydro-1-naphthols and 2-substituted 1-naphthols. The Journal of Organic Chemistry. 71: 4810-7. PMID 16776506 DOI: 10.1021/Jo060299P |
0.559 |
|
2004 |
Chen CL, Martin SF. Facile synthesis of 2-substituted 1,2-dihydro-1-naphthols and 2-substituted 1-naphthols. Organic Letters. 6: 3581-4. PMID 15387553 DOI: 10.1021/Ol048517T |
0.537 |
|
2002 |
Chen C, Chen Y, Liu Y, Peng S, Liu S. Initiation Steps for the Polymerization of Vinyl Ethers Promoted by Cationic Palladium Aqua Complexes Organometallics. 21: 5382-5385. DOI: 10.1021/Om020662S |
0.353 |
|
2001 |
Chen Y, Chen C, Chen J, Liu S. Well-Controlled Block Polymerization/Copolymerization of Alkenes and/or Carbon Monoxide by Cationic Palladium Methyl Complexes Organometallics. 20: 1285-1286. DOI: 10.1021/Om001070H |
0.319 |
|
1999 |
Reddy KR, Chen C, Liu Y, Peng S, Chen J, Liu S. New Imine−Phosphine Palladium Complexes Catalyze Copolymerization of CO−Ethylene and CO−Norbornylene and Provide Well-Characterized Stepwise Insertion Intermediates of Various Unsaturated Substrates Organometallics. 18: 2574-2576. DOI: 10.1021/Om990222+ |
0.314 |
|
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