The core fragment C7-C15 the (+)-migrastatin was constructed in a stereoconvergent manner utilizing desymmetrization approach. The strategy involved the generation of Z-configuration of trisubstituted double bond at C11-C12, epimerization at C10, ring opening of the pyran lactol with C2 Wittig ylide, and regioselective Sharpless dihydroxylation
A stereoselective formal total synthesis of borrelidin is described. The synthetic strategy for synt...
Complestatin is a natural product that has demonstrated inhibition activity against HIV-1 integrase ...
The C(19)---C(31) fragment of the anti-tumor macrolide, scytophycin C, was realized in a stereoconve...
A migrastatina é um policetídeo que foi isolado da cultura de Streptomyces sp. MK929-43F1 em 2000 po...
<p>Reagents and conditions: (a) 5-hexenoic acid, Ph <sub>3</sub>P, DIAD, PhCH<sub>3</sub>, rt, 3h, 6...
Synthesis of the C1-C11 tetrahydropyran core unit of (+)-zincophorin using a desymmetrization strate...
The unique core structure of the complex pentacyclic 5,11-methanomorphanthridine has been constructe...
A highly stereoselective and convergent approach for the key intermediate of the FGHI ring system of...
Migrastatin is a secondary metabolite that is formed from the bacterium Streptomyces platensis. This...
We describe herein a short and efficient synthesis of the C1-C9 fragment of the potent antitumor age...
An approach to the asymmetric synthesis of fragments corresponding to C1---C7 and C15---C24 of (+)-d...
This dissertation describes progress towards the synthesis of spirastrellolide E, a potent cytotoxic...
The convergent synthesis of the C12-C24 fragment (lower part) of macrolactin A is described. The ad...
The spirastrellolides are a novel family of structurally unprecedented marine macrolides which show ...
Migrastatin and isomigrastatin analogues have been synthesised in order to contribute to structure-a...
A stereoselective formal total synthesis of borrelidin is described. The synthetic strategy for synt...
Complestatin is a natural product that has demonstrated inhibition activity against HIV-1 integrase ...
The C(19)---C(31) fragment of the anti-tumor macrolide, scytophycin C, was realized in a stereoconve...
A migrastatina é um policetídeo que foi isolado da cultura de Streptomyces sp. MK929-43F1 em 2000 po...
<p>Reagents and conditions: (a) 5-hexenoic acid, Ph <sub>3</sub>P, DIAD, PhCH<sub>3</sub>, rt, 3h, 6...
Synthesis of the C1-C11 tetrahydropyran core unit of (+)-zincophorin using a desymmetrization strate...
The unique core structure of the complex pentacyclic 5,11-methanomorphanthridine has been constructe...
A highly stereoselective and convergent approach for the key intermediate of the FGHI ring system of...
Migrastatin is a secondary metabolite that is formed from the bacterium Streptomyces platensis. This...
We describe herein a short and efficient synthesis of the C1-C9 fragment of the potent antitumor age...
An approach to the asymmetric synthesis of fragments corresponding to C1---C7 and C15---C24 of (+)-d...
This dissertation describes progress towards the synthesis of spirastrellolide E, a potent cytotoxic...
The convergent synthesis of the C12-C24 fragment (lower part) of macrolactin A is described. The ad...
The spirastrellolides are a novel family of structurally unprecedented marine macrolides which show ...
Migrastatin and isomigrastatin analogues have been synthesised in order to contribute to structure-a...
A stereoselective formal total synthesis of borrelidin is described. The synthetic strategy for synt...
Complestatin is a natural product that has demonstrated inhibition activity against HIV-1 integrase ...
The C(19)---C(31) fragment of the anti-tumor macrolide, scytophycin C, was realized in a stereoconve...