The stereoselective total synthesis of (+)−cardiobutanolide, a polyhydroxylated natural product, is achieved in high yield through Lu and Guo diene synthesis, Sharpless asymmetric dihydroxylation, and one-pot deprotection-lactonization. The utility of a recyclable reagent system in PEG for asymmetric dihydroxylation is demonstrated
The asymmetric syntheses of novel dihydroxyhomoprolines have been achieved using the doubly diastere...
International audienceToward the synthesis of FR225654, an antidiabetic natural product, the Sharple...
An efficient asymmetric synthesis of (+)-tetrahydropseudodistomin is described. The important synthe...
A short protecting-group-free synthesis of (+)-cardiobutanolide is reported. We have modified a one-...
A formal total synthesis of (+)-cardiobutanolide has been accomplished from D-glucose, a readily ava...
The naturally occurring styryllactone (+)-cardiobutanolide has been synthesized in a highly efficien...
Stereoselective synthesis of styryllactone (+)-cardiobutanolide was accomplished in good overall yie...
Sharpless asymmetric dihydroxylation involves the reaction of an alkene with osmium tetroxide in the...
Stereoselective synthesis of styryllactone (+)-cardiobutanolide was accomplished in good overall yie...
This thesis describes the development of chiral auxiliary based methodologies for the asymmetric syn...
An efficient and highly stereoselective asymmetric synthesis of C1-C9 and C9-C17 fragments of (+)-13...
Asymmetric total synthesis of structurally intriguing and highly oxygenated lancifodilactone G aceta...
Access restricted to the OSU CommunityA flexible, convergent-divergent strategy for the asymmetric t...
We have developed a protocol incuding dynamic kinetic resolution as the key step for the asymmetric ...
Polyhydroxylated fragments are ubiquitous in natural products possessing interesting biological prop...
The asymmetric syntheses of novel dihydroxyhomoprolines have been achieved using the doubly diastere...
International audienceToward the synthesis of FR225654, an antidiabetic natural product, the Sharple...
An efficient asymmetric synthesis of (+)-tetrahydropseudodistomin is described. The important synthe...
A short protecting-group-free synthesis of (+)-cardiobutanolide is reported. We have modified a one-...
A formal total synthesis of (+)-cardiobutanolide has been accomplished from D-glucose, a readily ava...
The naturally occurring styryllactone (+)-cardiobutanolide has been synthesized in a highly efficien...
Stereoselective synthesis of styryllactone (+)-cardiobutanolide was accomplished in good overall yie...
Sharpless asymmetric dihydroxylation involves the reaction of an alkene with osmium tetroxide in the...
Stereoselective synthesis of styryllactone (+)-cardiobutanolide was accomplished in good overall yie...
This thesis describes the development of chiral auxiliary based methodologies for the asymmetric syn...
An efficient and highly stereoselective asymmetric synthesis of C1-C9 and C9-C17 fragments of (+)-13...
Asymmetric total synthesis of structurally intriguing and highly oxygenated lancifodilactone G aceta...
Access restricted to the OSU CommunityA flexible, convergent-divergent strategy for the asymmetric t...
We have developed a protocol incuding dynamic kinetic resolution as the key step for the asymmetric ...
Polyhydroxylated fragments are ubiquitous in natural products possessing interesting biological prop...
The asymmetric syntheses of novel dihydroxyhomoprolines have been achieved using the doubly diastere...
International audienceToward the synthesis of FR225654, an antidiabetic natural product, the Sharple...
An efficient asymmetric synthesis of (+)-tetrahydropseudodistomin is described. The important synthe...
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