A short stereoselective total synthesis of the fusarium toxin equisetin.
A short stereoselective synthesis of the fusarium toxin equisetin, an N-methylserine-derived acyl tetramic acid and potent inhibitor of HIV-1 integrase enzyme, is described using as the key step a stereoselective lithium perchlorate mediated intramolecular Diels-Alder reaction of a fully conjugated...
Main Authors: | Burke, LT, Dixon, D, Ley, S, Rodríguez, F |
---|---|
格式: | Journal article |
语言: | English |
出版: |
2000
|
相似书籍
-
Total synthesis of the Fusarium toxin equisetin.
由: Burke, LT, et al.
出版: (2005) -
A short and efficient stereoselective synthesis of the polyhydroxylated macrolactone (+)-aspicillin
由: Dixon, D, et al.
出版: (2000) -
A short and efficient stereoselective synthesis of the potent 5-lipoxygenase inhibitor CMI-977
由: Dixon, D, et al.
出版: (2000) -
A short and efficient stereoselective synthesis of the potent 5-lipoxygenase inhibitor, CMI-977
由: Dixon, D, et al.
出版: (2001) -
A short and efficient stereoselective synthesis of the potent 5-lipoxygenase inhibitor, CMI-977
由: Dixon, D, et al.
出版: (2001)