A synthesis of the pleuromutilin antibiotic SB-268091 is described which includes a new and improved route to the quinuclidine-4-thiol ligand. This chemistry has been run on multikilo scale and involved a reductive double debenzylation using sodium in liquid ammonia. Alternative conditions have been developed to prepare quinuclidine-4-thiol which avoid the use of sodium in liquid ammonia. The generality of this process to prepare differentially <i>S</i>-protected quinuclidine-4-thiols is also discussed and exemplified by the preparation of a range of analogues
Throughout history natural products have served as a valuable resource for the treatment of various ...
© 2018 by the authors. A convenient approach to the synthesis of multithiacalix[4]arene derivatives ...
A novel synthetic method using an original and practical procedure for the preparation of the N-PNZ ...
An improved synthesis of an eneimide, which is a useful precursor to pleuromutilin-based antibiotics...
An 18-step synthesis of the antibiotic (+)-pleuromutilin is disclosed. The key steps of the synthesi...
A novel method for cleavage of the dithiine ring in 5,12-(dimethyl)-thioqinantrenium bis-chloride 1 ...
This dissertation details the development of a synthetic route to the pleuromutilin diterpenes and t...
Pleuromutilin is a fungal diterpene natural product with antimicrobial properties, semisynthetic der...
A simple and efficient protocol for the synthesis of Nβ- Fmoc/Z-amino alkyl thiols is described. Th...
and their sulfur analogs (DHPMs) have attracted consider-able interest due to their pharmaceutical p...
The total synthesis of the marine alkaloid variolin B has been achieved in eight steps, starting fro...
The work detailed in this thesis is directed towards the synthesis of natural products exhibiting an...
Chapter 1 describes, in a schematic manner, various approaches to the synthesis of the repeating dis...
Due to increasing resistance to pharmaceuticals among infectious bacterial strains and cancers, it h...
The compound class of 2-alkyl-4(1H)-quinolones represents a unique group of bacterial secondary meta...
Throughout history natural products have served as a valuable resource for the treatment of various ...
© 2018 by the authors. A convenient approach to the synthesis of multithiacalix[4]arene derivatives ...
A novel synthetic method using an original and practical procedure for the preparation of the N-PNZ ...
An improved synthesis of an eneimide, which is a useful precursor to pleuromutilin-based antibiotics...
An 18-step synthesis of the antibiotic (+)-pleuromutilin is disclosed. The key steps of the synthesi...
A novel method for cleavage of the dithiine ring in 5,12-(dimethyl)-thioqinantrenium bis-chloride 1 ...
This dissertation details the development of a synthetic route to the pleuromutilin diterpenes and t...
Pleuromutilin is a fungal diterpene natural product with antimicrobial properties, semisynthetic der...
A simple and efficient protocol for the synthesis of Nβ- Fmoc/Z-amino alkyl thiols is described. Th...
and their sulfur analogs (DHPMs) have attracted consider-able interest due to their pharmaceutical p...
The total synthesis of the marine alkaloid variolin B has been achieved in eight steps, starting fro...
The work detailed in this thesis is directed towards the synthesis of natural products exhibiting an...
Chapter 1 describes, in a schematic manner, various approaches to the synthesis of the repeating dis...
Due to increasing resistance to pharmaceuticals among infectious bacterial strains and cancers, it h...
The compound class of 2-alkyl-4(1H)-quinolones represents a unique group of bacterial secondary meta...
Throughout history natural products have served as a valuable resource for the treatment of various ...
© 2018 by the authors. A convenient approach to the synthesis of multithiacalix[4]arene derivatives ...
A novel synthetic method using an original and practical procedure for the preparation of the N-PNZ ...