F. Guibé

发表

Palladium- and molybdenum-catalyzed hydrostannation of alkynes: a novel access to regio- and stereodefined vinylstannanes

H. X. Zhang, F. Guibé, G. Balavoine, 1990 .

N α -Alloc temporary protection in solid-phase peptide synthesis. The use of amine–borane complexes as allyl group scavengers

F. Albericio, F. Guibé, Paloma Gomez-Martinez, 1999 .

Use of Alloc-amino acids in solid-phase peptide synthesis. Tandem deprotection-coupling reactions using neutral conditions

E. Giralt, F. Albericio, J. Alsina, 1997 .

New allyl group acceptors for palladium catalyzed removal of allylic protections and transacylation of allyl carbamates

F. Guibé, M. Dessolin, N. Thieriet, 1995 .

Investigation of SmI2-mediated cyclisation of δ-iodo-α,β-unsaturated esters by deuterium 2D NMR in oriented solvents

F. Guibé, P. Lesot, C. Aroulanda, 2002 .

Diastereoselective SmI2-mediated cyclisation of δ-oxo-α,β-unsaturated esters to cyclopropanols

F. Guibé, H. Villar, 2002 .

SmI2-Mediated 3-exo-trig cyclisation of δ-oxo-α,β-unsaturated esters to cyclopropanols and derivatives

Riadh Zriba, F. Guibé, Sophie Bezzenine-Lafollée, 2004 .

A new access to ring-fused cyclopropanols through samarium diiodide-induced 3-exo-trig-cyclisations

Riadh Zriba, F. Guibé, Caroline Magnier-Bouvier, 2007 .

The allyloxycarbonyl group for alcohol protection: quantitative removal or transformation into allyl protecting group via π-allyl complexes of palladium

F. Guibé, Y. M'leux, 1982 .

Reduction of some polyhalogenato- and polyacetoxy-allylic compunds using tributyltin hydride in the presence or absence of palladium catalyst: II. Reduction of 1,1,1,4-tetrachlorobut-2-ene☆

Y. Xian, F. Guibé, G. Balavoine, 1986 .

Reduction of some polyhalogenato- and polyacetoxy- alyllic compounds with tributylin hydride in the presence or absence of a palladium catalyst

F. Guibé, G. Balavoine, A. Zigna, 1986 .

Allylic protecting groups and their use in a complex environment part II: Allylic protecting groups and their removal through catalytic palladium π-allyl methodology

F. Guibé, 1998 .

Allylic protecting groups and their use in a complex environment part I: Allylic protection of alcohols

F. Guibé, 1997 .

An access to (Z)-ethylenic pseudodipeptides based on ring-closing metathesis

H. Sauriat-Dorizon, F. Guibé, V. Boucard, 2002 .

Allylic protection of thiols and cysteine: II: The N-[2,3,5,6-tetrafluoro-4-(N′-piperidino)-phenyl], N-allyloxycarbonylaminomethyl (Fnam) group

A. Kimbonguila, F. Guibé, Paloma Gomez-Martinez, 1999 .

Solid-phase peptide synthesis in the reverse (N --> C) direction.

F. Albericio, F. Guibé, N. Thieriet, 2000, Organic letters.

The allyloxycarbonyl group for alcohol protection: quantitative removal or transformation into allyl protecting group via π-allyl complexes of palladium

F. Guibé, Y. M'leux, 1981 .

Palladium catalyzed hydrostannation of alkynes and palladium-catalyzed hydrostannolysis of propargyl or propargyloxycarbonyl derivatives of various functional groups

F. Guibé, G. Balavoine, Hui‐Jun Zhang, 1988 .

Palladium-catalyzed reaction of tributyltin hydride. Selective and very mild deprotection of allyl and allyloxycarbonyl derivatives of amino-acids

O. Dangles, F. Guibé, G. Balavoine, 1986 .

Regio- and stereoselective reductive opening of diene-ester derived monoepoxides with palladium catalyst and dimethylamine–borane complex

F. Guibé, M. Guillerez, Hervé David, 2000 .

Enantioconservative synthesis and ring closing metathesis of disubstituted dialkenic amides

H. Sauriat-Dorizon, F. Guibé, 1998 .

New potential access to ethylenic pseudodipeptides through catalytic alkene metathesis

F. Guibé, F. Garro-Hélion, 1996 .

Mild and selective palladium(0)-catalyzed deallylation of allylic amines. Allylamine and diallylamine as very convenient ammonia equivalents for the synthesis of primary amines

F. Guibé, A. Merzouk, F. Garro-Hélion, 1993 .

Palladium-catalyzed reaction of tributyltin hydride with acyl chlorides. A mild, selective, and general route to aldehydes

F. Guibé, P. Four, 1981 .

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

O. Dangles, S. Lavielle, F. Guibé, 1987 .

Ring Closing Metathesis of Unsaturated Amides as a Route to Short and Medium-Sized Unsaturated Lactams and to Ethylenic Pseudopeptides

H. Sauriat-Dorizon, G. Vo‐Thanh, F. Guibé, 2001 .

Selective palladium-catalyzed deprotection of the allyl and allyloxycarbonyl groups in phosphate chemistry and in the presence of propargyl and propargyloxycarbonyl groups

F. Guibé, G. Balavoine, Hui‐Jun Zhang, 1988 .

Tandem deprotection-coupling of Nα-Alloc-amino acids by use of ternary systems Pd cat./PhSiH3/carboxy-activated amino acid

F. Guibé, Paloma Gomez-Martinez, N. Thieriet, 1999 .

Palladium-catalysed reaction of tributyltin hydride with acyl chlorides. A selective route to aldehydes

F. Guibé, H. Rivière, P. Four, 1980 .

Regio‐ and Stereoselective Reductive Opening of Diene‐Ester Derived Monoepoxides with Palladium Catalyst and Dimethylamine—Borane Complex.

F. Guibé, M. Guillerez, Hervé David, 2000 .

Cyclopropane ring formation by an SmI2 mediated cyclisation of δ-halo-α,β-unsaturated esters

C. Afonso, F. Guibé, M. Bonin, 1999 .

Oxidatively induced nucleophilic capture vs. degradation of cyclopentadienyl iron derivatives of simple carboxylic acids and of α-amino acids. A comparative study

C. Amiens, F. Guibé, G. Balavoine, 1993 .

Oxidatively induced radical chemistry of dicarbonyl η5-cyclopentadienyl iron derivatives of carboxylic acids (Fp–acyl complexes)

C. Amiens, F. Guibé, G. Balavoine, 1991 .

2-Cyano Δ3piperideine VII1 : the condensation of 2-cyano Δ3piperideine with sodium dimethylmalonate catalyzed by ZnCl2 or zero valent palladium and platinum complexes

D. Grierson, F. Guibé, H. Husson, 1982 .

On the allyl protection of the imidazole ring of histidine

A. Kimbonguila, F. Guibé, A. Loffet, 1997 .

The allyloxycarbonylaminomethyl group: a new allytic protection for the thiol group of cysteine

A. Kimbonguila, F. Guibé, A. Loffet, 1994 .

Solid-phase synthesis of peptides using allylic anchoring groups 2. Palladium-catalysed cleavage of Fmoc-protected peptides☆☆☆

E. Giralt, F. Albericio, P. Lloyd-Williams, 1994 .

Allylic protection of thiols and cysteine: I: The allyloxycarbonylaminomethyl group

A. Kimbonguila, F. Guibé, A. Loffet, 1999 .

Carbon acidity. 53. Kinetic and equilibrium acidities of fluorinated bicycloalkanes

A. Streitwieser, F. Guibé, J. Stoffer, 1976 .

Carbon acidity. 62. Equilibrium acidities of some phenalene hydrocarbons: SCF-.pi. MO correlation

J. Word, James S. Wright, A. Streitwieser, 1981 .

A Very Efficient and Straight Forward Synthesis of 1,3-Dichloro 1,1,3,3-Tetraisopropyl Disiloxane

H. X. Zhang, F. Guibé, G. Balavoine, 1987 .

On the use of silylated nucleophiles in the palladium catalysed deprotection of allylic carboxylates and carbamates.

F. Guibé, A. Loffet, A. Merzouk, 1992 .

Use of an allylic anchor group and of its palladium catalyzed hydrostannolytic cleavage in the solid phase synthesis of protected peptide fragments

O. Dangles, F. Guibé, G. Balavoine, 1989 .

Reactivity of cyclopropanic δ-oxo-α,β-unsaturated esters towards SmI2: 3-exo-trig cyclisation versus cyclopropane ring opening

Riadh Zriba, F. Guibé, Sophie Bezzenine-Lafollée, 2007 .

A perturbational interpretation of enolate alkylation: C/O selectivity and electrophile leaving group effect.

A. Loupy, J. Lefour, G. Bram, 1978 .

Carbon acidity. 56. Equilibrium acidities of 4-methyl-, 4-ethyl-, and 4-isopropylbiphenyls with cesium cyclohexylamide

A. Streitwieser, F. Guibé, 1978 .

Selective Cleavage of the Allyl and Allyloxycarbonyl Groups Through Palladium-Catalyzed Hydrostannolysis with Tributyltin Hydride. Application to the Selective Protection-Deprotection of Amino Acid Derivatives and in Peptide Synthesis

O. Dangles, S. Lavielle, F. Guibé, 1988 .

Allylic protection of thiols and cysteine. III. Use of Fmoc-Cys(Fsam)-OH for solid-phase peptide synthesis

F. Albericio, F. Guibé, Paloma Gomez-Martinez, 2000, Letters in Peptide Science.