By utilizing an l-serine-derived bicyclic lactone as an advanced chiral building block, a short synthetic route to the cytotoxic marine natural product jaspine B has been developed. Targeting structure–activity relationship investigations, the synthetic route has also been utilized for the synthesis and cytotoxicity evaluation of strategically modified jaspine B analogues. In addition, a previously reported synthesis of the title natural product from our research has been reinvestigated to clarify the sterochemical assignment
A practical stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine...
A short route for the synthesis of Pachastrissamine (Jaspine B), an anhydrosphingosine derivative, a...
The jerantinine family of Aspidosperma indole alkaloids from Tabernaemontana corymbosa are potent mi...
By utilizing an l-serine-derived bicyclic lactone as an advanced chiral building block, a short synt...
Jaspine B (pachastrissamine), which was isolated in 2002, is a naturally occurring anhydrophytosphin...
Tetrahydrofurans and pyrrolidines are important structural motifs that are found in a variety of nat...
A short, 8-step synthesis of the marine natural product pachastrissamine has been developed that rel...
Part I. HIV Protease Targeted Synthesis of Conformationally–Rigid Hydroxyethylene Dipeptide Is...
(R)-tert-butyl (1-hydroxybut-3-yn-2-yl)carbamate, an key intermediate of the natural product jaspine...
International audienceA straightforward access to pyrrolidine-based analogues of jaspine B was devel...
A theoretical study to elucidate the mechanistic aspects involved in the tosylation-cyclization reac...
Producción CientíficaChirality is determinant for sphingosine biofunctions and pharmacological activ...
The thesis entitled “Total synthesis of bio-active natural products microcarpalide, synargentolide A...
A practical stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine...
This dissertation comprises the design, synthesis, and biological evaluation of nine new jasplakinol...
A practical stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine...
A short route for the synthesis of Pachastrissamine (Jaspine B), an anhydrosphingosine derivative, a...
The jerantinine family of Aspidosperma indole alkaloids from Tabernaemontana corymbosa are potent mi...
By utilizing an l-serine-derived bicyclic lactone as an advanced chiral building block, a short synt...
Jaspine B (pachastrissamine), which was isolated in 2002, is a naturally occurring anhydrophytosphin...
Tetrahydrofurans and pyrrolidines are important structural motifs that are found in a variety of nat...
A short, 8-step synthesis of the marine natural product pachastrissamine has been developed that rel...
Part I. HIV Protease Targeted Synthesis of Conformationally–Rigid Hydroxyethylene Dipeptide Is...
(R)-tert-butyl (1-hydroxybut-3-yn-2-yl)carbamate, an key intermediate of the natural product jaspine...
International audienceA straightforward access to pyrrolidine-based analogues of jaspine B was devel...
A theoretical study to elucidate the mechanistic aspects involved in the tosylation-cyclization reac...
Producción CientíficaChirality is determinant for sphingosine biofunctions and pharmacological activ...
The thesis entitled “Total synthesis of bio-active natural products microcarpalide, synargentolide A...
A practical stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine...
This dissertation comprises the design, synthesis, and biological evaluation of nine new jasplakinol...
A practical stereoselective synthesis of cytotoxic anhydrophytosphingosine pachastrissamine (jaspine...
A short route for the synthesis of Pachastrissamine (Jaspine B), an anhydrosphingosine derivative, a...
The jerantinine family of Aspidosperma indole alkaloids from Tabernaemontana corymbosa are potent mi...