International audienceA convergent synthetic approach of the highly cytotoxic natural product (−)-callystatin A was developed assembling three fragments through Julia-Kocienski olefination and Stille cross-coupling. The new strategy relies on a pivotal local symmetry of the target molecule. In this preliminary study, particular attention was devoted to facilitate the catalytic enantiocontrol of strategic stereogenic centers present in each of the fragments
A novel synthetic approach towards the recently reported anti-tumor and anti-tuberculor natural prod...
We wish to describe here our continuing efforts towards the total synthesis of the marine sponge pol...
The stereoselective oxidative coupling of cyclic ketones via silyl bis-enol ethers followed by ring-...
International audienceA convergent synthetic approach of the highly cytotoxic natural product (−)-ca...
The stereoselective synthesis of the two major fragments (C1 -C6 and C7 -C22) of cytotoxic polyketid...
A highly convergent and stereocontrolled total synthesis of (−)-callystatin A 1, a member of the lep...
Callyspongiolide is a marine natural product which displays very potent antiproliferative properties...
An asymmetric total synthesis of the aminocyclopentitol pactamycin is described. The title compound ...
A highly convergent and efficient total synthesis of the potent antitumor polyketide (-)-callystatin...
A highly convergent and efficient total synthesis of the potent antitumor polyketide (-)-callystatin...
Orientador: Luiz Carlos DiasTese (doutorado) - Universidade Estadual de Campinas, Instituto de Quimi...
An efficient synthesis of the polypropionate framework of callystatin A has been achieved by utilizi...
Matteson homologations of chiral boronic esters proved to be an excellent tool for the synthesis of ...
An asymmetric total synthesis of the aminocyclopentitol pactamycin is described, which delivers the ...
A novel synthetic approach towards the recently reported anti-tumor and anti-tuberculor natural prod...
A novel synthetic approach towards the recently reported anti-tumor and anti-tuberculor natural prod...
We wish to describe here our continuing efforts towards the total synthesis of the marine sponge pol...
The stereoselective oxidative coupling of cyclic ketones via silyl bis-enol ethers followed by ring-...
International audienceA convergent synthetic approach of the highly cytotoxic natural product (−)-ca...
The stereoselective synthesis of the two major fragments (C1 -C6 and C7 -C22) of cytotoxic polyketid...
A highly convergent and stereocontrolled total synthesis of (−)-callystatin A 1, a member of the lep...
Callyspongiolide is a marine natural product which displays very potent antiproliferative properties...
An asymmetric total synthesis of the aminocyclopentitol pactamycin is described. The title compound ...
A highly convergent and efficient total synthesis of the potent antitumor polyketide (-)-callystatin...
A highly convergent and efficient total synthesis of the potent antitumor polyketide (-)-callystatin...
Orientador: Luiz Carlos DiasTese (doutorado) - Universidade Estadual de Campinas, Instituto de Quimi...
An efficient synthesis of the polypropionate framework of callystatin A has been achieved by utilizi...
Matteson homologations of chiral boronic esters proved to be an excellent tool for the synthesis of ...
An asymmetric total synthesis of the aminocyclopentitol pactamycin is described, which delivers the ...
A novel synthetic approach towards the recently reported anti-tumor and anti-tuberculor natural prod...
A novel synthetic approach towards the recently reported anti-tumor and anti-tuberculor natural prod...
We wish to describe here our continuing efforts towards the total synthesis of the marine sponge pol...
The stereoselective oxidative coupling of cyclic ketones via silyl bis-enol ethers followed by ring-...