The stereoselective total synthesis of (+)-pinellic acid, a natural product used in the treatment of influenza, was accomplished from L-(+)-tartaric acid. A key feature of the synthesis includes the elaboration of a γ-hydroxybutyramide derived from L-(+)-tartaric acid
A straightforward strategy for the synthesis of (+)-pinellic acid in 16% overall yield and 13 steps,...
A stereoselective synthesis of the C1-C18 region of marine natural product palmerolide A from chiral...
A stereoselective approach for the synthesis of the bio-active decanolactone (−)-microcarpalide was ...
The stereoselective total synthesis of (+)-pinellic acid, a natural product used in the treatment of...
Abstract—Pinellic acid is a novel and potentially useful oral adjuvant when used in conjunction with...
The total synthesis of (9S,12R,13S)-pinellic acid, a novel and potentially useful oral adjuvant, iso...
The total synthesis of (-)-pinellic acid with (9S,12S,13S)-configuration and its (9R,12S,13S)-diaste...
Stereoselective synthesis of (-)-9-deoxygoniopypyrone was achieved from the naturally occurring L-(+...
Stereoselective synthesis of (-)-9-deoxygoniopypyrone was achieved from the naturally occurring L-(+...
Stereoselective formal synthesis of (−)-centrolobine was achieved from naturally occurring L-(+)-tar...
A stereoselective synthesis of the C1-C18 region of marine natural product palmerolide A from chiral...
A formal total synthesis of (-)-didemniserinolipid B from L-(+)-tartaric acid is presented. Key feat...
A formal total synthesis of (-)-didemniserinolipid B from L-(+)-tartaric acid is presented. Key fe...
Chiral protected and deprotected amides were synthesized by using commercially available L-tartaric ...
A straightforward strategy for the synthesis of (+)-pinellic acid in 16% overall yield and 13 steps,...
A straightforward strategy for the synthesis of (+)-pinellic acid in 16% overall yield and 13 steps,...
A stereoselective synthesis of the C1-C18 region of marine natural product palmerolide A from chiral...
A stereoselective approach for the synthesis of the bio-active decanolactone (−)-microcarpalide was ...
The stereoselective total synthesis of (+)-pinellic acid, a natural product used in the treatment of...
Abstract—Pinellic acid is a novel and potentially useful oral adjuvant when used in conjunction with...
The total synthesis of (9S,12R,13S)-pinellic acid, a novel and potentially useful oral adjuvant, iso...
The total synthesis of (-)-pinellic acid with (9S,12S,13S)-configuration and its (9R,12S,13S)-diaste...
Stereoselective synthesis of (-)-9-deoxygoniopypyrone was achieved from the naturally occurring L-(+...
Stereoselective synthesis of (-)-9-deoxygoniopypyrone was achieved from the naturally occurring L-(+...
Stereoselective formal synthesis of (−)-centrolobine was achieved from naturally occurring L-(+)-tar...
A stereoselective synthesis of the C1-C18 region of marine natural product palmerolide A from chiral...
A formal total synthesis of (-)-didemniserinolipid B from L-(+)-tartaric acid is presented. Key feat...
A formal total synthesis of (-)-didemniserinolipid B from L-(+)-tartaric acid is presented. Key fe...
Chiral protected and deprotected amides were synthesized by using commercially available L-tartaric ...
A straightforward strategy for the synthesis of (+)-pinellic acid in 16% overall yield and 13 steps,...
A straightforward strategy for the synthesis of (+)-pinellic acid in 16% overall yield and 13 steps,...
A stereoselective synthesis of the C1-C18 region of marine natural product palmerolide A from chiral...
A stereoselective approach for the synthesis of the bio-active decanolactone (−)-microcarpalide was ...
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