AAAAAA

   
Results: 1-11 |
Results: 11
ENANTIOCONSERVATIVE SYNTHESIS AND RING CLOSING METATHESIS OF DISUBSTITUTED DIALKENIC AMIDES
Authors: SAURIATDORIZON H GUIBE F
Citation: H. Sauriatdorizon et F. Guibe, ENANTIOCONSERVATIVE SYNTHESIS AND RING CLOSING METATHESIS OF DISUBSTITUTED DIALKENIC AMIDES, Tetrahedron letters, 39(37), 1998, pp. 6711-6714
ALLYLIC PROTECTING GROUPS AND THEIR USE IN A COMPLEX ENVIRONMENT - PART 1 - ALLYLIC PROTECTION OF ALCOHOLS (VOL 53, PG 13509, 1997)
Authors: GUIBE F
Citation: F. Guibe, ALLYLIC PROTECTING GROUPS AND THEIR USE IN A COMPLEX ENVIRONMENT - PART 1 - ALLYLIC PROTECTION OF ALCOHOLS (VOL 53, PG 13509, 1997), Tetrahedron, 54(15), 1998, pp. 3645-3645
ALLYLIC PROTECTING GROUPS AND THEIR USE IN A COMPLEX ENVIRONMENT - PART II - ALLYLIC PROTECTING GROUPS AND THEIR REMOVAL THROUGH CATALYTIC PALLADIUM PI-ALLYL METHODOLOGY
Authors: GUIBE F
Citation: F. Guibe, ALLYLIC PROTECTING GROUPS AND THEIR USE IN A COMPLEX ENVIRONMENT - PART II - ALLYLIC PROTECTING GROUPS AND THEIR REMOVAL THROUGH CATALYTIC PALLADIUM PI-ALLYL METHODOLOGY, Tetrahedron, 54(13), 1998, pp. 2967-3042
USE OF ALLOC-AMINO ACIDS IN SOLID-PHASE PEPTIDE-SYNTHESIS - TANDEM DEPROTECTION-COUPLING REACTIONS USING NEUTRAL CONDITIONS
Authors: THIERIET N ALSINA J GIRALT E GUIBE F ALBERICIO F
Citation: N. Thieriet et al., USE OF ALLOC-AMINO ACIDS IN SOLID-PHASE PEPTIDE-SYNTHESIS - TANDEM DEPROTECTION-COUPLING REACTIONS USING NEUTRAL CONDITIONS, Tetrahedron letters, 38(41), 1997, pp. 7275-7278
ALLYLIC PROTECTING GROUPS AND THEIR USE IN A COMPLETE ENVIRONMENT .1.ALLYLIC PROTECTION OF ALCOHOLS
Authors: GUIBE F
Citation: F. Guibe, ALLYLIC PROTECTING GROUPS AND THEIR USE IN A COMPLETE ENVIRONMENT .1.ALLYLIC PROTECTION OF ALCOHOLS, Tetrahedron, 53(40), 1997, pp. 13509-13556
ON THE ALLYL PROTECTION OF THE IMIDAZOLE RING OF HISTIDINE
Authors: KIMBONGUILA AM BOUCIDA S GUIBE F LOFFET A
Citation: Am. Kimbonguila et al., ON THE ALLYL PROTECTION OF THE IMIDAZOLE RING OF HISTIDINE, Tetrahedron, 53(37), 1997, pp. 12525-12538
NEW POTENTIAL ACCESS TO ETHYLENIC PSEUDODIPEPTIDES THROUGH CATALYTIC ALKENE METATHESIS
Authors: GARROHELION F GUIBE F
Citation: F. Garrohelion et F. Guibe, NEW POTENTIAL ACCESS TO ETHYLENIC PSEUDODIPEPTIDES THROUGH CATALYTIC ALKENE METATHESIS, Chemical communications, (5), 1996, pp. 641-642
NEW ALLYL GROUP ACCEPTERS FOR PALLADIUM-CATALYZED REMOVAL OF ALLYLIC PROTECTIONS AND TRANSACYLATION OF ALLYL CARBAMATES
Authors: DESSOLIN M GUILLEREZ MG THIERIET N GUIBE F LOFFET A
Citation: M. Dessolin et al., NEW ALLYL GROUP ACCEPTERS FOR PALLADIUM-CATALYZED REMOVAL OF ALLYLIC PROTECTIONS AND TRANSACYLATION OF ALLYL CARBAMATES, Tetrahedron letters, 36(32), 1995, pp. 5741-5744
THE ALLYLOXYCARBONYLAMINOMETHYL GROUP - A NEW ALLYLIC PROTECTION FOR THE THIOL-GROUP OF CYSTEINE
Authors: KIMBONGUILA AM MERZOUK A GUIBE F LOFFET A
Citation: Am. Kimbonguila et al., THE ALLYLOXYCARBONYLAMINOMETHYL GROUP - A NEW ALLYLIC PROTECTION FOR THE THIOL-GROUP OF CYSTEINE, Tetrahedron letters, 35(48), 1994, pp. 9035-9038
SOLID-PHASE SYNTHESIS OF PEPTIDES USING ALLYLIC ANCHORING GROUPS .2. PALLADIUM-CATALYZED CLEAVAGE OF FMOC-PROTECTED PEPTIDES
Authors: LLOYDWILLIAMS P MERZOUK A GUIBE F ALBERICIO F GIRALT E
Citation: P. Lloydwilliams et al., SOLID-PHASE SYNTHESIS OF PEPTIDES USING ALLYLIC ANCHORING GROUPS .2. PALLADIUM-CATALYZED CLEAVAGE OF FMOC-PROTECTED PEPTIDES, Tetrahedron letters, 35(25), 1994, pp. 4437-4440
MILD AND SELECTIVE PALLADIUM(0)-CATALYZED DEALLYLATION OF ALLYLIC AMINES - ALLYLAMINE AND DIALLYLAMINE AS VERY CONVENIENT AMMONIA EQUIVALENTS FOR THE SYNTHESIS OF PRIMARY AMINES
Authors: GARROHELION F MERZOUK A GUIBE F
Citation: F. Garrohelion et al., MILD AND SELECTIVE PALLADIUM(0)-CATALYZED DEALLYLATION OF ALLYLIC AMINES - ALLYLAMINE AND DIALLYLAMINE AS VERY CONVENIENT AMMONIA EQUIVALENTS FOR THE SYNTHESIS OF PRIMARY AMINES, Journal of organic chemistry, 58(22), 1993, pp. 6109-6113
Risultati: 1-11 |