Jaspine B (pachastrissamine), which was isolated in 2002, is a naturally occurring anhydrophytosphingosine which displays potent biological activity, and as such has attracted much attention from synthetic chemists in recent years, with 14 syntheses reported to date. This review delineates the isolation of jaspine B, and laboratory total syntheses of jaspine B, 2-epi-jaspine B and analogues, which serves to confirm their structure and stereochemistry. © 2008 Elsevier Ltd. All rights reserved
Chirality is determinant for sphingosine biofunctions and pharmacological activity, yet the reasons ...
Taspine is an alkaloid found in the latex of certain trees belonging to the family of Euphorbiaceae,...
A theoretical study to elucidate the mechanistic aspects involved in the tosylation-cyclization reac...
By utilizing an l-serine-derived bicyclic lactone as an advanced chiral building block, a short synt...
A short, 8-step synthesis of the marine natural product pachastrissamine has been developed that rel...
A practical stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine...
A practical stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine...
A short route for the synthesis of Pachastrissamine (Jaspine B), an anhydrosphingosine derivative, a...
Tetrahydrofurans and pyrrolidines are important structural motifs that are found in a variety of nat...
The total synthesis of the enantiomer of the tetrahydrofuran containing natural product Jaspine B is...
International audienceA straightforward access to pyrrolidine-based analogues of jaspine B was devel...
Synthesis of both enantiomers of pachastrissamine is described from a common chiral template. The st...
The highly diastereoselective conjugate addition of lithium (S)-N-benzyl-N-(alpha-methylbenzyl)amide...
The highly diastereoselective anti-aminohydroxylation of (E)-gamma-tri-iso-propylsilyloxy-alpha,beta...
The highly diastereoselective anti-aminohydroxylation of (E)-gamma-tri-iso-propylsilyloxy-alpha,beta...
Chirality is determinant for sphingosine biofunctions and pharmacological activity, yet the reasons ...
Taspine is an alkaloid found in the latex of certain trees belonging to the family of Euphorbiaceae,...
A theoretical study to elucidate the mechanistic aspects involved in the tosylation-cyclization reac...
By utilizing an l-serine-derived bicyclic lactone as an advanced chiral building block, a short synt...
A short, 8-step synthesis of the marine natural product pachastrissamine has been developed that rel...
A practical stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine...
A practical stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine...
A short route for the synthesis of Pachastrissamine (Jaspine B), an anhydrosphingosine derivative, a...
Tetrahydrofurans and pyrrolidines are important structural motifs that are found in a variety of nat...
The total synthesis of the enantiomer of the tetrahydrofuran containing natural product Jaspine B is...
International audienceA straightforward access to pyrrolidine-based analogues of jaspine B was devel...
Synthesis of both enantiomers of pachastrissamine is described from a common chiral template. The st...
The highly diastereoselective conjugate addition of lithium (S)-N-benzyl-N-(alpha-methylbenzyl)amide...
The highly diastereoselective anti-aminohydroxylation of (E)-gamma-tri-iso-propylsilyloxy-alpha,beta...
The highly diastereoselective anti-aminohydroxylation of (E)-gamma-tri-iso-propylsilyloxy-alpha,beta...
Chirality is determinant for sphingosine biofunctions and pharmacological activity, yet the reasons ...
Taspine is an alkaloid found in the latex of certain trees belonging to the family of Euphorbiaceae,...
A theoretical study to elucidate the mechanistic aspects involved in the tosylation-cyclization reac...