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Results: 1-8 |
Results: 8
HIGHLY STEREOSELECTIVE TRANS ADDITION OF PI-TYPE NUCLEOPHILES TO A BICYCLIC N-ACYLIMINIUM ION - APPLICATION TO THE SYNTHESIS OF INDOLIZIDINE AND PYRROLIZIDINE ALKALOIDS
Authors: DHIMANE H VANUCCIBACQUE C HAMON L LHOMMET G
Citation: H. Dhimane et al., HIGHLY STEREOSELECTIVE TRANS ADDITION OF PI-TYPE NUCLEOPHILES TO A BICYCLIC N-ACYLIMINIUM ION - APPLICATION TO THE SYNTHESIS OF INDOLIZIDINE AND PYRROLIZIDINE ALKALOIDS, EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, (9), 1998, pp. 1955-1963
STEREOCONTROLLED ADDITION OF PI-TYPE NUCLEOPHILES TO A BICYCLIC N-ACYLIMINIUM ION - NEW ACCESS TO TRANS-2,6-DISUBSTITUTED PIPERIDINE SUBSTRUCTURES
Authors: DAVID M DHIMANE H VANUCCIBACQUE C LHOMMET G
Citation: M. David et al., STEREOCONTROLLED ADDITION OF PI-TYPE NUCLEOPHILES TO A BICYCLIC N-ACYLIMINIUM ION - NEW ACCESS TO TRANS-2,6-DISUBSTITUTED PIPERIDINE SUBSTRUCTURES, Synlett, (2), 1998, pp. 206
SYNTHESIS OF INDOLIZIDINES (-)-195B, (-)-223AB AND (-)-239AB - BONYL]-2-METHOXYCARBONYL-5-(4-PENTENYL)PYRROLIDINE AS A VERSATILE CHIRAL BUILDING-BLOCK
Authors: CELIMENE C DHIMANE H LHOMMET G
Citation: C. Celimene et al., SYNTHESIS OF INDOLIZIDINES (-)-195B, (-)-223AB AND (-)-239AB - BONYL]-2-METHOXYCARBONYL-5-(4-PENTENYL)PYRROLIDINE AS A VERSATILE CHIRAL BUILDING-BLOCK, Tetrahedron, 54(35), 1998, pp. 10457-10468
SYNTHESIS OF NEW TRIALKYLSILYLMETHYLOXAZINONES VIA INTRAMOLECULAR TRAPPING OF BETA-SILYL CARBOCATIONS BY AN N-BOC GROUP
Authors: BROCHERIEUXLANOY S DHIMANE H POUPON JC VANUCCI C LHOMMET G
Citation: S. Brocherieuxlanoy et al., SYNTHESIS OF NEW TRIALKYLSILYLMETHYLOXAZINONES VIA INTRAMOLECULAR TRAPPING OF BETA-SILYL CARBOCATIONS BY AN N-BOC GROUP, Journal of the Chemical Society. Perkin transactions. I, (15), 1997, pp. 2163-2165
STEREOSELECTIVE ACCESS TO TRANS-2,5-DISUBSTITUTED PYRROLIDINE DERIVATIVES BY NUCLEOPHILIC-ADDITION TO BICYCLIC N-ACYLIMINIUM ION
Authors: DHIMANE H VANUCCI C LHOMMET G
Citation: H. Dhimane et al., STEREOSELECTIVE ACCESS TO TRANS-2,5-DISUBSTITUTED PYRROLIDINE DERIVATIVES BY NUCLEOPHILIC-ADDITION TO BICYCLIC N-ACYLIMINIUM ION, Tetrahedron letters, 38(8), 1997, pp. 1415-1418
UNEXPECTED DIASTEREOSELECTIVITY IN THE FORMATION OF 3,5-DISUBSTITUTEDINDOLIZIDINES BY INTRAMOLECULAR REDUCTIVE AMINATION
Authors: CELIMENE C DHIMANE H SABOUREAU A LHOMMET G
Citation: C. Celimene et al., UNEXPECTED DIASTEREOSELECTIVITY IN THE FORMATION OF 3,5-DISUBSTITUTEDINDOLIZIDINES BY INTRAMOLECULAR REDUCTIVE AMINATION, Tetrahedron : asymmetry, 7(6), 1996, pp. 1585-1588
TANDEM ZINC MEDIATED REDUCTIVE CLEAVAGE REDUCTIVE AMINATION AS A NEW APPROACH TO SUBSTITUTED PYRROLIDINES FROM HOMOALLYLIC AMINES
Authors: VANUCCI C BRUSSON X VERDEL V ZANA F DHIMANE H LHOMMET G
Citation: C. Vanucci et al., TANDEM ZINC MEDIATED REDUCTIVE CLEAVAGE REDUCTIVE AMINATION AS A NEW APPROACH TO SUBSTITUTED PYRROLIDINES FROM HOMOALLYLIC AMINES, Tetrahedron letters, 36(17), 1995, pp. 2971-2974
A SHORT AND HIGHLY STEREOCONTROLLED TOTAL SYNTHESIS OF (3R,5R,8AR)-3-N-BUTYL-5-METHYLINDOLIZIDINE
Authors: CELIMENE C DHIMANE H LEBAIL M LHOMMET G
Citation: C. Celimene et al., A SHORT AND HIGHLY STEREOCONTROLLED TOTAL SYNTHESIS OF (3R,5R,8AR)-3-N-BUTYL-5-METHYLINDOLIZIDINE, Tetrahedron letters, 35(33), 1994, pp. 6105-6106
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