An intramolecular aryne Diels–Alder reaction with a furan moiety was applied to the synthesis of dihydrobenzo[<i>de</i>]isochromenes as intermediates toward naphthalimides. After oxidation, this method offers an efficient approach for the synthesis of substituted naphthalimides, which showed potent cytotoxic activity against HT-29 human cancer cell line
In this article the molecular design and chemical synthesis of a series of enediynes (12-19, Chart I...
A novel, highly efficient method generally applicable to the synthesis of both syn- and anti-diol ep...
Base-mediated decomposition of amide-substituted furfuryl tosylhydrazones afforded practical access ...
International audienceAn intramolecular aryne Diels-Alder reaction with a furan moiety was applied t...
A series of 2,3-diyne-1,4-naphthoquinone derivatives was synthesized from 2,3-dibromo- 1,4-naphthoq...
The direct assembly of benzo[<i>c</i>]carbazole derivatives via the Diels–Alder reaction of arynes...
The highly efficient and expedient route for the syntheses of 2-aroyl benzofurans has been developed...
Arynes are known as useful synthons in organic synthesis. In particular, reactions accompanying mult...
Alkylating agents represent a class of chemotherapeutic anticancer agents used in the treatment of c...
The search for novel chemotherapeutic agents and approaches to cancer treatment is an active researc...
The work described in this thesis focused on developing a method to synthesise a variety of organic ...
The dihydropyranoindole structures were previously identified as promising scaffolds for improving t...
Summary: The development of efficient synthetic strategies for the discovery of novel antitumor mole...
498-507The catalytic application of AgOTf for the regioselective cycloisomerization of 2-(alkynyl)...
We report the efficient synthesis involving palladium-catalyzed reactions and biological evaluation ...
In this article the molecular design and chemical synthesis of a series of enediynes (12-19, Chart I...
A novel, highly efficient method generally applicable to the synthesis of both syn- and anti-diol ep...
Base-mediated decomposition of amide-substituted furfuryl tosylhydrazones afforded practical access ...
International audienceAn intramolecular aryne Diels-Alder reaction with a furan moiety was applied t...
A series of 2,3-diyne-1,4-naphthoquinone derivatives was synthesized from 2,3-dibromo- 1,4-naphthoq...
The direct assembly of benzo[<i>c</i>]carbazole derivatives via the Diels–Alder reaction of arynes...
The highly efficient and expedient route for the syntheses of 2-aroyl benzofurans has been developed...
Arynes are known as useful synthons in organic synthesis. In particular, reactions accompanying mult...
Alkylating agents represent a class of chemotherapeutic anticancer agents used in the treatment of c...
The search for novel chemotherapeutic agents and approaches to cancer treatment is an active researc...
The work described in this thesis focused on developing a method to synthesise a variety of organic ...
The dihydropyranoindole structures were previously identified as promising scaffolds for improving t...
Summary: The development of efficient synthetic strategies for the discovery of novel antitumor mole...
498-507The catalytic application of AgOTf for the regioselective cycloisomerization of 2-(alkynyl)...
We report the efficient synthesis involving palladium-catalyzed reactions and biological evaluation ...
In this article the molecular design and chemical synthesis of a series of enediynes (12-19, Chart I...
A novel, highly efficient method generally applicable to the synthesis of both syn- and anti-diol ep...
Base-mediated decomposition of amide-substituted furfuryl tosylhydrazones afforded practical access ...