Michel Sylvie | Laboratoire De Pharmacognosie De I'universite Rene Descartes U.m.r. C.n.r.s. N° 8638 Faculte De

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著作論文

Synthesis and Cytotoxic Activity of Dimeric Analogs of Acronycine in the Benzo[b]pyrano[3,2-h]acridin-7-one Series
Design, Synthesis, and Cytotoxic Activity of Michael Acceptors and Enol Esters in the Benzo[b]acronycine Series
Synthesis and Cytotoxic and Antitumor Activity of 1,2-Dihydroxy-1,2-dihydrobenzo[b]acronycine Diacid Hemiesters and Carbamates
Design, Synthesis and Biological Activity of 7-O-(4-O-Acetyl-3-iodo-2,3,6-trideoxy-α-L-arabino-hexopyranosyl)daunomycinone and 7-O-(3-Chloro-2,3,6-trideoxy-4-O-propanoyl-α-L-lyxo-hexopyranosyl)daunomycinone
Synthesis and Cytotoxic Activity of Benzo[a]pyrano[3,2-h] and [2,3-i]xanthone Analogues of Psorospermine, Acronycine, and Benzo [a] acronycine
Synthesis and Cytotoxic Activity of Pyranocarbazole Analogues of Ellipticine and Acronycine
Synthesis and Cytotoxic Activity of Benzopyranoxanthone Analogues of Benzo[b]acronycine and Psorospermine
Synthesis and Cytotoxic Activity of 11-Nitro and 11-Amino Derivatives of Acronycine and 6-Demethoxyacronycine
Synthesis and Cytotoxic Activity of 1-Alkoxy- and 1-Amino-2-hydroxy-1,2-dihydroacronycine Derivatives
Synthesis and Cytotoxic Activity of Acronycine Derivatives Modified at the Pyran Ring
Megistoquinones I and II, Two Quinoline Alkaloids with Antibacterial Activity from the Bark of Sarcomelicope megistophylla
Synthesis and Cytotoxic Activity of Isoacronycine and Its Derivatives
1-Oxo-2-hydroxy-1, 2-dihydroacronycine : A Useful Synthon in the Acronycine Series for the Introduction of Amino Substituents at 6-Position and for the Conversion into Isopropylfuroacridones
Two New 3-Methoxy-4-quinolone Alkaloids from the Bark of Sarcomelicope megistophylla
A New Sphingolipid and Furanocoumarins with Antimicrobial Activity from Ficus exasperata

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