Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Philip W. Le Quesne"'
Natural product chemistry has undergone an explosive growth during the latter half of the current century. This has been brought about by a number of factors. One of these has been the growing number of sub stances from natural sources which displa
Autor:
Magdi M. Moussa, Philip W. Le Quesne
Publikováno v:
Tetrahedron Letters. 37:6479-6482
The total synthesis of pithomycolide 1 , a structurally unique ionophoric depsipeptide from the fungus Pithomyces chartarum , is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5711687526c304bcfedfb639cac5d87
https://doi.org/10.1016/0040-4039(96)01421-9
https://doi.org/10.1016/0040-4039(96)01421-9
Autor:
Shao-Xia Yu, Philip W. Le Quesne
Publikováno v:
Tetrahedron Letters. 36:6205-6208
The total synthesis of (±) - funebral 5 , a sterically crowded, rotationally restricted pyrrole alkaloid, has been achieved by means of a new variation of the Paal-Knorr synthesis, employing titanium isopropoxide.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbdb37ab6ac533c34a3ff6e03dc1cf54
https://doi.org/10.1016/0040-4039(95)01250-l
https://doi.org/10.1016/0040-4039(95)01250-l
Publikováno v:
Natural Product Letters. 6:77-80
The characteristic metabolites of Quararibea funebris are based on (2S, 3S, 4R)-γ-hydroxyisoleucine, a hitherto rare amino acid. Two new stereoselective and efficient syntheses of this compound are described; one is based on Claisen chemistry and th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::473a972072e62466459d2b204156df4a
https://doi.org/10.1080/10575639508044091
https://doi.org/10.1080/10575639508044091
Autor:
Sheri L. Ablaza, Philip W. Le Quesne, Simon Bolvig, Ying Dong, David A. Forsyth, Shao-Xia Yu, Niranjan N. Pai
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5564502ae39910772b837532e8101c27
https://doi.org/10.1002/chin.199933241
https://doi.org/10.1002/chin.199933241
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb1cbf7141d7eeb8ffba3ddab9e679c9
https://doi.org/10.1002/chin.200012275
https://doi.org/10.1002/chin.200012275
Autor:
Ying Dong, Philip W. Le Quesne
Publikováno v:
ChemInform. 33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe860a906b92347edacea2a89cd29cc3
https://doi.org/10.1002/chin.200222196
https://doi.org/10.1002/chin.200222196
Publikováno v:
The Journal of Organic Chemistry. 57:2100-2104
New synthetic sequences are described for 17β-hydroxy-1β,2β- and -1α,2α-epoxyestr-4-en-3-one, which are putative intermediates in the metabolism of estradiol to the 2,3- and 3,4-catecholestrogens, as well as the synthetic precursors of choice fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f13ba54855041226eafa55e136236395
https://doi.org/10.1021/jo00033a035
https://doi.org/10.1021/jo00033a035
Publikováno v:
Journal of natural products. 71(8)
The first enantiospecific total synthesis of (+)-alstonisine has been accomplished from D-tryptophan methyl ester 13 in 12% overall yield (in 17 reaction vessels). A diastereospecific osmylation process has been employed as a key step to convert indo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ef0109328caf721e2a11f7212ad4e87
https://pubmed.ncbi.nlm.nih.gov/18611051
https://pubmed.ncbi.nlm.nih.gov/18611051
Publikováno v:
Tetrahedron Letters. 31:2681-2684
The first synthesis of (+) pseudophrynaminol, a unique pyrrolo [2,3b] indole recently isolated from the Australian frog Pseudophryne coriacea, is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0fcb7effb6dd86037a9fd82e58e4f1fb
https://doi.org/10.1016/s0040-4039(00)94671-9
https://doi.org/10.1016/s0040-4039(00)94671-9