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Results: 1-13 |
Results: 13
APPLICATION OF THE PD-CATALYZED HETEROARYLATION TO THE SYNTHESIS OF 5-(INDOL-2'-YL)PYRIDIN-2-ONE AND 5-(INDOL-2'-YL)PYRAN-2-ONE
Authors: DANIELI B LESMA G MARTINELLI M PASSARELLA D PERETTO I SILVANI A
Citation: B. Danieli et al., APPLICATION OF THE PD-CATALYZED HETEROARYLATION TO THE SYNTHESIS OF 5-(INDOL-2'-YL)PYRIDIN-2-ONE AND 5-(INDOL-2'-YL)PYRAN-2-ONE, Tetrahedron, 54(46), 1998, pp. 14081-14088
VINBLASTINE-TYPE ANTITUMOR ALKALOIDS - A METHOD FOR CREATING NEW C17 MODIFIED ANALOGS
Authors: DANIELI B LESMA G MARTINELLI M PASSARELLA D SILVANI A
Citation: B. Danieli et al., VINBLASTINE-TYPE ANTITUMOR ALKALOIDS - A METHOD FOR CREATING NEW C17 MODIFIED ANALOGS, Journal of organic chemistry, 63(23), 1998, pp. 8586-8588
HIGHLY ENANTIOPURE C-1-SYMMETRICAL CIS-PIPERIDINE-3,5-DIMETHANOL MONOACETATES BY ENZYMATIC ASYMMETRIZATION
Authors: DANIELI B LESMA G PASSARELLA D SILVANI A
Citation: B. Danieli et al., HIGHLY ENANTIOPURE C-1-SYMMETRICAL CIS-PIPERIDINE-3,5-DIMETHANOL MONOACETATES BY ENZYMATIC ASYMMETRIZATION, Journal of organic chemistry, 63(10), 1998, pp. 3492-3496
CANDIDA-ANTARCTICA LIPASE-B CATALYZES THE REGIOSELECTIVE ESTERIFICATION OF ECDYSTEROIDS AT THE C-2 OH
Authors: DANIELI B LESMA G LUISETTI M RIVA S
Citation: B. Danieli et al., CANDIDA-ANTARCTICA LIPASE-B CATALYZES THE REGIOSELECTIVE ESTERIFICATION OF ECDYSTEROIDS AT THE C-2 OH, Tetrahedron, 53(16), 1997, pp. 5855-5862
AN EXPEDITIOUS SYNTHESIS OF DIMETHYL 1-BENZYL-CIS-PIPERIDINE-3,5-DICARBOXYLATE
Authors: DANIELI B LESMA G PASSARELLA D SILVANI A
Citation: B. Danieli et al., AN EXPEDITIOUS SYNTHESIS OF DIMETHYL 1-BENZYL-CIS-PIPERIDINE-3,5-DICARBOXYLATE, Synthetic communications, 27(1), 1997, pp. 69-77
DIASTEREOSELECTIVE SYNTHESIS OF 3-OXO-14,15-DIHYDROANDRANGININE
Authors: DANIELI B LESMA G MARTINELLI M PASSARELLA D SILVANI A
Citation: B. Danieli et al., DIASTEREOSELECTIVE SYNTHESIS OF 3-OXO-14,15-DIHYDROANDRANGININE, Journal of organic chemistry, 62(19), 1997, pp. 6519-6523
STEREOSELECTIVE ENZYMATIC-HYDROLYSIS OF DIMETHYL MESO-PIPERIDINE-3,5-DICARBOXYLATES
Authors: DANIELI B LESMA G PASSARELLA D SILVANI A
Citation: B. Danieli et al., STEREOSELECTIVE ENZYMATIC-HYDROLYSIS OF DIMETHYL MESO-PIPERIDINE-3,5-DICARBOXYLATES, Tetrahedron : asymmetry, 7(2), 1996, pp. 345-348
DIELS-ALDER REACTIONS OF METHYL N-P-METHOXYBENZENSULFONYLINDOLE-2-(2-PROPENOATE), A CONVENIENT DIENOPHILE TOWARDS THE SYNTHESIS OF ANDRANGININE
Authors: DANIELI B LESMA G LUZZANI M PASSARELLA D SILVANI A
Citation: B. Danieli et al., DIELS-ALDER REACTIONS OF METHYL N-P-METHOXYBENZENSULFONYLINDOLE-2-(2-PROPENOATE), A CONVENIENT DIENOPHILE TOWARDS THE SYNTHESIS OF ANDRANGININE, Tetrahedron, 52(34), 1996, pp. 11291-11296
A CONVENIENT APPROACH TO THE N-SUBSTITUTED AMINO DIENES, N-BENZYL-5-ETHENYL-3,4-DIHYDROPYRIDIN-2-ONE AND N-CBZ-5-ETHENYL-1,2,3,4-TETRAHYDROPYRIDINE
Authors: BIGOGNO C DANIELI B LESMA G PASSARELLA D
Citation: C. Bigogno et al., A CONVENIENT APPROACH TO THE N-SUBSTITUTED AMINO DIENES, N-BENZYL-5-ETHENYL-3,4-DIHYDROPYRIDIN-2-ONE AND N-CBZ-5-ETHENYL-1,2,3,4-TETRAHYDROPYRIDINE, Heterocycles, 41(5), 1995, pp. 973-982
FIRST ENANTIOSELECTIVE SYNTHESIS OF (-)-AKAGERINE BY A CHEMOENZYMATICAPPROACH
Authors: DANIELI B LESMA G MAURO M PALMISANO G PASSARELLA D
Citation: B. Danieli et al., FIRST ENANTIOSELECTIVE SYNTHESIS OF (-)-AKAGERINE BY A CHEMOENZYMATICAPPROACH, Journal of organic chemistry, 60(8), 1995, pp. 2506-2513
A HIGHLY ENANTIOSELECTIVE SYNTHESIS OF (-)-ANTIRHINE BY CHEMOENZYMATIC APPROACH
Authors: DANIELI B LESMA G MAURO M PALMISANO G PASSARELLA D
Citation: B. Danieli et al., A HIGHLY ENANTIOSELECTIVE SYNTHESIS OF (-)-ANTIRHINE BY CHEMOENZYMATIC APPROACH, Tetrahedron, 50(29), 1994, pp. 8837-8852
ASPIDOSPERMA ALKALOIDS VIA CYCLIZATION OF SECODINE INTERMEDIATE - SYNTHESIS OF (+ -)-3-OXOVINCADIFFORMINE ETHYL-ESTER/
Authors: DANIELI B LESMA G PALMISANO G PASSARELLA D SILVANI A
Citation: B. Danieli et al., ASPIDOSPERMA ALKALOIDS VIA CYCLIZATION OF SECODINE INTERMEDIATE - SYNTHESIS OF (+ -)-3-OXOVINCADIFFORMINE ETHYL-ESTER/, Tetrahedron, 50(23), 1994, pp. 6941-6954
FUNCTIONALIZATION AT C-17 OF AN EBURNEA-ASPIDOSPERMA BINARY ALKALOID AS A MODEL TO STUDY MODIFIED VINBLASTINE-TYPE ANTITUMOR ALKALOIDS
Authors: DANIELI B LESMA G PALMISANO G PASSARELLA D PYUSKYULEV B NGOC TM
Citation: B. Danieli et al., FUNCTIONALIZATION AT C-17 OF AN EBURNEA-ASPIDOSPERMA BINARY ALKALOID AS A MODEL TO STUDY MODIFIED VINBLASTINE-TYPE ANTITUMOR ALKALOIDS, Journal of organic chemistry, 59(19), 1994, pp. 5810-5813
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