M. Mondon

发表

Synthetic studies on a phenyl-laulimalide analogue

U. Koert, Christelle Faveau, M. Mondon, 2006 .

Synthesis of novel targeted pro-prodrugs of anthracyclines potentially activated by a monoclonal antibody galactosidase conjugate (part 1)

C. Monneret, J. Florent, P. Petit, 1992 .

HEXASUBSTITUTED TRIPHENYLENES : A NEW MESOMORPHIC ORDER

C. Destrade, M. C. Mondon, J. Malthete, 1979 .

Development of New Triazolyl-Based Acidic Sensitive Releasing Systems

C. Len, C. Bachmann, P. Bertrand, 2012 .

Novel triazolyl derivatives for acidic release of amines

C. Bachmann, P. Bertrand, G. Frapper, 2011 .

Triazolyl Derivatives for Acidic Release of Alcohols

C. Len, C. Bachmann, P. Bertrand, 2011 .

Prodrugs of anthracyclines for use in antibody-directed enzyme prodrug therapy.

C. Monneret, J. Florent, F. Tillequin, 1998, Journal of medicinal chemistry.

Prodrugs of anthracyclines for chemotherapy via enzyme-monoclonal antibody conjugates.

P. Petit, F. Tillequin, B. Renoux, 1994, Anti-cancer drug design.

Synthesis and structure of novel cyclonucleoside analogues of uridine

C. Len, S. Pilard, M. Mondon, 2008 .

Synthesis of novel dinucleosides via tandem cross-metathesis and ring-closing metathesis

C. Len, S. Pilard, M. Mondon, 2006 .

Synthesis of quinone and xanthone analogs of rhein

H. Ficheux, M. Mondon, J. Gesson, 2001 .

The photochemical addition of N-haloamides to olefins: the influence of various factors on the competition between 1,2-addition and hydrogen abstraction

J. Lessard, D. Touchard, M. Mondon, 1981 .

Towards a stable noeuromycin analog with a D-manno configuration: synthesis and glycosidase inhibition of D-manno-like tri- and tetrahydroxylated azepanes.

D. Alonzi, T. Butters, Yongming Zhang, 2012, Bioorganic & medicinal chemistry.

Synthesis and cytotoxic activity of tetracenomycin D and of saintopin analogues.

P. Renard, B. Pfeiffer, B. Renoux, 2002, Bioorganic & medicinal chemistry.

Selective cross-metathesis of 2-allylphenols with styrenes

M. Mondon, J. Gesson, Nadia Fonteneau, 2001 .

Selective trihydroxyazepane NagZ inhibitors increase sensitivity of Pseudomonas aeruginosa to β-lactams.

A. Oliver, D. Vocadlo, B. Mark, 2013, Chemical communications.

N- and C-alkylation of seven-membered iminosugars generates potent glucocerebrosidase inhibitors and F508del-CFTR correctors.

J. Marrot, D. Alonzi, T. Butters, 2014, Organic & biomolecular chemistry.

Skeletal rearrangement of seven-membered iminosugars: synthesis of (-)-adenophorine, (-)-1-epi-adenophorine and derivatives and evaluation as glycosidase inhibitors.

J. Guillard, Y. Blériot, S. Nakagawa, 2013, Bioorganic & medicinal chemistry.

Enantiodivergent synthesis of (+) and (−) altholactone from D-glucose. Preparation and cytotoxic activity of analogs

J. Jacquesy, M. Mondon, Jean-Plerre Gesson, 1989 .

Total synthesis of (−) altholactone (goniothalenol) from D-glucose

J. Jacquesy, M. Mondon, Jean-Plerre Gesson, 1987 .

Diels-Alder reaction of 4-bromo-6-spiroepoxycyclohexa-2,4-dienone with electron-rich and neutral dienophiles

C. Bachmann, A. Cousson, M. Mondon, 1999 .

Regioselective dienolate formation and alkylation of alkyl 2-methyl cyclohexene-1 carboxylates

J. Jacquesy, M. Mondon, J. Gesson, 1980 .

A general route to 11-deoxyanthracyclines

J. Jacquesy, M. Mondon, J. Gesson, 1980 .

Access to L- and D-iminosugar C-glycosides from a D-gluco-derived 6-azidolactol exploiting a ring isomerization/alkylation strategy.

J. Marrot, J. Désiré, J. Guillard, 2012, Organic letters.

Chiral synthesis of the hydroxy amino acid moiety of AI-77-B

J. Jacquesy, M. Mondon, Jean-Plerre Gesson, 1989 .

Cyclodimerization and Diels–Alder reaction of a spiroepoxycyclohexadienone with an o-quinodimethane structure

A. Cousson, M. Mondon, J. Gesson, 1999 .

Cyclodimerization and Diels—Alder Reaction of a Spiroepoxycyclohexadienone with an o-Quinodimethane Structure.

A. Cousson, M. Mondon, J. Gesson, 2010 .

Diels-Alder reaction of cyclopentadiene and spiroepoxy-2,4-cyclohexadienones

M. Mondon, Jean-Plerre Gesson, L. Hervaud, 1993 .

Synthesis of a novel uridine analogue and its use in attempts to form new cyclonucleosides using ring-closing metathesis

C. Len, M. Mondon, S. Zhong, 2010 .

Cycloaddition of Ketene Acetals with 4-Bromo-6-spiroepoxycyclohexa-2,4-dienone

M. Mondon, J. Gesson, N. Boeker, 1999 .

Diels-Alder Reaction of Cyclopentadiene (II) and Spiroepoxy-2,4- cyclohexadienones (I).

M. Mondon, Jean-Plerre Gesson, L. Hervaud, 1993 .

Release of the cyano moiety in the crystal structure of N-cyanomethyl-N-(2-methoxyethyl)-daunomycin complexed with d(CGATCG).

A. Dautant, G. Précigoux, M. Mondon, 1999, European journal of biochemistry.

Total synthesis of 11-deoxydaunomycinone

M. Mondon, J. Gesson, 1982 .

A short synthesis of L-fucose and analogs from D-mannose

P. Petit, J. Jacquesy, M. Mondon, 1992 .

A Short Synthesis of L‐Fucose and Analogs from D‐Mannose.

P. Petit, J. Jacquesy, M. Mondon, 1992 .

Anthracyclines. II - regiospecific synthesis of 6-deoxyanthracycline intermediates☆

J. Jacquesy, M. Mondon, J. Gesson, 1981 .