Palladium-catalyzed reactions in aqueous media. An efficient removal of allyloxycarbonyl protecting group from oxygen and nitrogen

[1]  F. Guibé,et al.  On the use of silylated nucleophiles in the palladium catalysed deprotection of allylic carboxylates and carbamates. , 1992 .

[2]  D. Sinou,et al.  Palladium(0)-Catalyzed Substitution of Allylic Substrates in a Two-Phase Aqueous-Organic Medium , 1991 .

[3]  Joseph C. Calabrese,et al.  Palladium-catalyzed alkylations in aqueous media , 1990 .

[4]  Yoshihiro Hayakawa,et al.  The allylic protection method in solid-phase oligonucleotide synthesis. An efficient preparation of solid-anchored DNA oligomers , 1990 .

[5]  Y. Tanigawa,et al.  Palladium(0)-catalyzed azidation of allyl esters. Selective synthesis of allyl azides, primary allylamines, and related compounds , 1989 .

[6]  O. Dangles,et al.  Use of an allylic anchor group and of its palladium catalyzed hydrostannolytic cleavage in the solid phase synthesis of protected peptide fragments , 1989 .

[7]  H. Waldmann,et al.  The Allyl Ester as Carboxy‐Protecting Group in the Stereoselective Construction of Neuraminic‐Acid Glycosides , 1988 .

[8]  J. Genêt,et al.  Synthesis of α -aminophosphonic acids by Pd(O) alkylation of diethyl aminomethylphosphonate schiff bases. , 1988 .

[9]  J. Genêt,et al.  Synthesis of α-amino acids using transition metal catalysis - alkylation of schiff bases derived from α-amimo acid esters (regio, stereo - selectivity) , 1988 .

[10]  O. Dangles,et al.  Selective cleavage of the allyl and (allyloxy)carbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesis , 1987 .

[11]  J. Genêt,et al.  Stereoselective synthesis of side chain of glaucasterol using palladium (O) catalyst. , 1987 .

[12]  J. Genêt,et al.  Bis (alrylsulfonyl)methane: A versatile synthon in pheromone synthesis , 1986 .

[13]  J. Tsuji.  New general synthetic methods involving π-allylpalladium complexes as intermediates and neutral reaction conditions , 1986 .

[14]  P. Boullanger,et al.  The N-allyloxycarbonyl derivative of D-glucosamine: a potent precursor of β-glycosidation. , 1986 .

[15]  I. Minami,et al.  Palladium-catalyzed reaction of allyl carbamates; allylation of carbonucleophiles, and protection-deprotection of amines , 1985 .

[16]  H. Kunz,et al.  The Allyloxycarbonyl (Aloc) Moiety—Conversion of an Unsuitable into a Valuable Amino Protecting Group for Peptide Synthesis† , 1984 .

[17]  J. Genêt,et al.  Alkylation d'α-nitroacetates catalysee par les complexesn3 du palladium , 1984 .

[18]  H. Waldmann,et al.  The Allyl Group as Mildly and Selectively Removable Carboxy‐Protecting Group for the Synthesis of Labile O‐Glycopeptides , 1984 .

[19]  J. Bäckvall,et al.  Regio-and stereoselective palladium catalyzed amination of allylic substrates. Synthesis of -4-amino-2-alken-1-ol derivatives , 1983 .

[20]  F. Guibé,et al.  The allyloxycarbonyl group for alcohol protection: quantitative removal or transformation into allyl protecting group via π-allyl complexes of palladium , 1982 .

[21]  B. Trost,et al.  A total synthesis of racemic and optically active ibogamine. Utilization and mechanism of a new silver ion assisted palladium catalyzed cyclization , 1978 .

[22]  B. Trost,et al.  Palladium catalyzed cyclizations to alkaloid skeletons. Facile synthesis of desethylibogamine , 1976 .