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Results: 1-14 |
Results: 14

Authors: Jin, FQ Wang, DJ Confalone, PN Pierce, ME Wang, Z Xu, GY Choudhury, A Nguyen, D
Citation: Fq. Jin et al., (2R,3S,5S)-2-acetoxy-3-fluoro-5-(p-toluoyloxymethyl)tetrahydrofuran: a keyintermediate for the practical synthesis of 9-(2,3-dideoxy-2-fluoro-beta-D-threo-pentofuranosyl)adenine (FddA), TETRAHEDR L, 42(29), 2001, pp. 4787-4789

Authors: Choudhury, A Pierce, ME Confalone, PN
Citation: A. Choudhury et al., Oxidative removal of p-methoxybenzyl-amino protecting group in the presence of a proximal hydroxy function: A solution to a process problem in SUSTIVA (R) (efavirenz) synthesis, SYN COMMUN, 31(23), 2001, pp. 3707-3714

Authors: Kauffman, GS Harris, GD Dorow, RL Stone, BRP Parsons, RL Pesti, JA Magnus, NA Fortunak, JM Confalone, PN Nugent, WA
Citation: Gs. Kauffman et al., An efficient chiral moderator prepared from inexpensive (+)3-carene: Synthesis of the HIV-1 non-nucleoside reverse transcriptase inhibitor DPC 963, ORG LETT, 2(20), 2000, pp. 3119-3121

Authors: Mousa, SA Forsythe, M Bozarth, J Jin, FQ Confalone, PN
Citation: Sa. Mousa et al., Human platelet alpha IIb beta 3 integrin binding affinity end specificity of SJ874: antiplatelet efficacy versus aspirin, CORON ART D, 11(7), 2000, pp. 563-570

Authors: Wang, Z Xu, GY Wang, DJ Pierce, ME Confalone, PN
Citation: Z. Wang et al., Chemoselective allylic addition of allyltrichlorosilane to alpha-oxocarboxylic acids: synthesis of tertiary alpha-hydroxy carboxylic acids, TETRAHEDR L, 41(23), 2000, pp. 4523-4526

Authors: Wang, Z Campagna, S Xu, GY Pierce, ME Fortunak, JM Confalone, PN
Citation: Z. Wang et al., A new and practical synthesis of vinyl dichlorides via a non-Wittig-type approach, TETRAHEDR L, 41(21), 2000, pp. 4007-4009

Authors: Jin, FQ Confalone, PN
Citation: Fq. Jin et Pn. Confalone, Palladium-catalyzed cyanation reactions of aryl chlorides, TETRAHEDR L, 41(18), 2000, pp. 3271-3273

Authors: Magnus, NA Confalone, PN Storace, L
Citation: Na. Magnus et al., A new asymmetric 1,4-addition method: application to the synthesis of the HIV non-nucleoside reverse transcriptase inhibitor DPC 961, TETRAHEDR L, 41(17), 2000, pp. 3015-3019

Authors: Wang, Z Campagna, S Yang, KH Xu, GY Pierce, ME Fortunak, JM Confalone, PN
Citation: Z. Wang et al., Practical preparation of terminal alkynes from aldehydes, J ORG CHEM, 65(6), 2000, pp. 1889-1891

Authors: Confalone, PN
Citation: Pn. Confalone, Principles of process research and chemical development in the pharmaceutical industry (vol 42, pg 3008, 1999), J MED CHEM, 43(26), 2000, pp. 5057-5057

Authors: Confalone, PN Jin, FQ Mousa, SA
Citation: Pn. Confalone et al., Platelet glycoprotein IIb/IIIa receptor antagonists derived from isoxazolidines, BIOORG MED, 9(1), 1999, pp. 55-58

Authors: Shatzmiller, S Confalone, PN Abiri, A
Citation: S. Shatzmiller et al., Coupling reagent dependent regioselectivity in the synthesis of lysine dipeptides, SYNLETT, 1999, pp. 963-965

Authors: Richards, LE Pieniaszek, HJ Shatzmiller, S Page, GO Blom, KF Read, JM Davidson, AF Confalone, PN
Citation: Le. Richards et al., Human moricizine metabolism. I. Isolation and identification of metabolites in human urine (vol 27, pg 217, 1997), XENOBIOTICA, 29(9), 1999, pp. 969-969

Authors: Confalone, PN Waltermire, RE
Citation: Pn. Confalone et Re. Waltermire, The process research and development of DuPont Merck's cyclic urea diols, a new class of HIV protease inhibitors, PROCESS CHEMISTRY IN THE PHARMACEUTICAL INDUSTRY, 1999, pp. 201-219
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