Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Christoph W. Wullschleger"'
Publikováno v:
Synlett. 27:2726-2730
Two dienes comprising the complete heavy-atom framework of the macrocyclic core of the marine macrolide leiodolide A were prepared by esterification of an appropriate carboxylic acid and two alcohol building blocks. The latter were obtained in a ster
Publikováno v:
Angewandte Chemie International Edition. 49:6936-6938
Publikováno v:
Angewandte Chemie. 122:7090-7092
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 19(39)
The stereoselective syntheses of 7,8,9-trideoxypeloruside A (4) and a monocyclic peloruside A analogue lacking the entire tetrahydropyran moiety (3) are described. The syntheses proceeded through the PMB-ether of an ω-hydroxy β-keto aldehyde as a c
Publikováno v:
ChemInform. 42
Publikováno v:
ChemInform. 41
This article provides an overview on the chemistry and structure–activity relationships of macrolide-based microtubule-stabilizing agents. The primary focus will be on the total synthesis or examples thereof, but a brief summary of the current stat
Publikováno v:
Organic letters. 12(5)
The stereoselective synthesis of the monocyclic peloruside A analogue 4 has been achieved, following a new efficient approach for the introduction of the side chain, involving a late-stage addition of vinyl lithium species 7a to aldehyde 8. Further k
Publikováno v:
Topics in Current Chemistry ISBN: 9783540690368
This article provides an overview on the chemistry and structure–activity relationships of macrolide-based microtubule-stabilizing agents. The primary focus will be on the total synthesis or examples thereof, but a brief summary of the current stat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36fe32de218fe3a835e4117794e59030
https://doi.org/10.1007/128_2008_9
https://doi.org/10.1007/128_2008_9