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Results: 1-10 |
Results: 10
A spectrophotometric-partial least squares (PLS-1) method for the simultaneous determination of furosemide and amiloride hydrochloride in pharmaceutical formulations
Authors: Ferraro, MCF Castellano, PM Kaufman, TS
Citation: Mcf. Ferraro et al., A spectrophotometric-partial least squares (PLS-1) method for the simultaneous determination of furosemide and amiloride hydrochloride in pharmaceutical formulations, J PHARM B, 26(3), 2001, pp. 443-451
Sulfonamidoacetal cyclization-based synthesis of a tetrahydrooxazaphenalenelactone related to the ABC-ring system of the stephaoxocanes
Authors: Kaufman, TS
Citation: Ts. Kaufman, Sulfonamidoacetal cyclization-based synthesis of a tetrahydrooxazaphenalenelactone related to the ABC-ring system of the stephaoxocanes, HETEROCYCLE, 55(2), 2001, pp. 323-330
Elaboration of 1-benzoyltetrahydroisoquinoline derivatives employing a Pictet-Spengler cyclization with alpha-chloro-alpha-phenylthioketones. Synthesis of O-methylvelucryptine
Authors: Silveira, CC Bernardi, CR Braga, AL Kaufman, TS
Citation: Cc. Silveira et al., Elaboration of 1-benzoyltetrahydroisoquinoline derivatives employing a Pictet-Spengler cyclization with alpha-chloro-alpha-phenylthioketones. Synthesis of O-methylvelucryptine, TETRAHEDR L, 42(51), 2001, pp. 8947-8950
Synthetic studies on natural stephaoxocanes. Elaboration of a tetrahydrooxazaphenalene potential intermediate
Authors: Kaufman, TS
Citation: Ts. Kaufman, Synthetic studies on natural stephaoxocanes. Elaboration of a tetrahydrooxazaphenalene potential intermediate, MOLECULES, 5(3), 2000, pp. 491-492
Elaboration of the isochromane system of stephaoxocanes employing an Oxa-Pictet Spengler type cyclization
Authors: Kaufman, TS Bernardi, CR Cipulli, M Silveira, CC
Citation: Ts. Kaufman et al., Elaboration of the isochromane system of stephaoxocanes employing an Oxa-Pictet Spengler type cyclization, MOLECULES, 5(3), 2000, pp. 493-494
Practical and efficient procedure for the in situ preparation of B-alkoxyoxazaborolidines. Enantioselective reduction of prochiral ketones
Authors: Ponzo, VL Kaufman, TS
Citation: Vl. Ponzo et Ts. Kaufman, Practical and efficient procedure for the in situ preparation of B-alkoxyoxazaborolidines. Enantioselective reduction of prochiral ketones, MOLECULES, 5(3), 2000, pp. 495-496
Electrophilic aromatic substitution by use of N-trosyliminium ions; Elaboration of 3-aryl tetrahydroisoquinolines
Authors: Bianchi, DA Kaufman, TS
Citation: Da. Bianchi et Ts. Kaufman, Electrophilic aromatic substitution by use of N-trosyliminium ions; Elaboration of 3-aryl tetrahydroisoquinolines, SYNLETT, (6), 2000, pp. 801-804
A tosyliminium ion-based total synthesis of (+/-)-schefferine
Authors: Bianchi, DA Kaufman, TS
Citation: Da. Bianchi et Ts. Kaufman, A tosyliminium ion-based total synthesis of (+/-)-schefferine, CAN J CHEM, 78(9), 2000, pp. 1165-1169
Pictet-Spengler condensation of N-sulfonyl-beta-phenethylamines with alpha-chloro-alpha-phenylselenoesters. New synthesis of 1,2,3,4-tetrahydroisoquinoline-1-carboxylates
Authors: Silveira, CC Bernardi, CR Braga, AL Kaufman, TS
Citation: Cc. Silveira et al., Pictet-Spengler condensation of N-sulfonyl-beta-phenethylamines with alpha-chloro-alpha-phenylselenoesters. New synthesis of 1,2,3,4-tetrahydroisoquinoline-1-carboxylates, TETRAHEDR L, 40(27), 1999, pp. 4969-4972
Diastereoselective alkoxymethylation of aromatic aldehydes with chiral lithiomethyl ethers. Synthesis of optically active monoprotected glycols
Authors: Ponzo, VL Kaufman, TS
Citation: Vl. Ponzo et Ts. Kaufman, Diastereoselective alkoxymethylation of aromatic aldehydes with chiral lithiomethyl ethers. Synthesis of optically active monoprotected glycols, CAN J CHEM, 76(10), 1998, pp. 1338-1343
Risultati: 1-10 |