Zobrazeno 1 - 10
of 278
pro vyhledávání: '"S.W. Pelletier"'
Autor:
S.W. Pelletier
Publikováno v:
Journal of Natural Products. 55:1-24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d276c6421e2eb3f0a3af582523155e2b
https://doi.org/10.1021/np50079a001
https://doi.org/10.1021/np50079a001
Autor:
S.W. Pelletier
Alkaloids: Chemical and Biological Perspectives, the 15th volume of the ACBP series, features four important reviews of research on alkaloids. Chapter 1 is the first comprehensive review of the carbon-13 and proton NMR shift assignments and physical
Publikováno v:
Tetrahedron. 31:1659-1665
The cycloaddition of diazoalkanes, diazoesters and diazoketones to 2(5H)-furanones followed by thermal decomposition of the respective adducts is shown to provide a general method for the preparation of a variety of alkylated 2(5H)-furanones. Reducti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95d3b992901adcfac00125659fb23746
https://doi.org/10.1016/0040-4020(75)85083-6
https://doi.org/10.1016/0040-4020(75)85083-6
Publikováno v:
Tetrahedron. 27:4417-4427
Tenuifolin (V), a prosapogenin isolated from the roots of P. tenuifolia and P. senega , has been shown to be 2β,27-dihydroxy-23-carboxyoleanolic acid 3β-O-glucoside, on the basis of physical data of tenuifolin and several of its degradation product
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76d59ceb9c9b27b49845f944c9f0b551
https://doi.org/10.1016/s0040-4020(01)98155-4
https://doi.org/10.1016/s0040-4020(01)98155-4
Publikováno v:
Phytochemistry. 7:625-635
A detailed study of the basic components of the roots of Aconitum heterophyllum has led to the isolation of seven new diterpene alkaloids. The weak base fraction yielded besides heteratisine, three more alkaloids designated as heterophyllisine, heter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6c8fb47e1b2f95a22415b49cfa05037
https://doi.org/10.1016/s0031-9422(00)88238-2
https://doi.org/10.1016/s0031-9422(00)88238-2
Autor:
S.W. Pelletier
Volume 13 of this series presents five timely reviews of research on alkaloids such as new developments in the chemistry and biology of alkaloids from amphibian skins. It provides a synopsis and tabulation of the hundreds of alkaloids that have been
Autor:
S.W. Pelletier, L.H. Keith
Publisher Summary This chapter discusses C19-diterpene alkaloids. The structures of the more complicated diterpene alkaloids may be subdivided into two general types that are closely related. The first is the lycoctonine-type that is based on the par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfebed7fff1913b5a74cc400730a22b4
https://doi.org/10.1016/s1876-0813(08)60100-1
https://doi.org/10.1016/s1876-0813(08)60100-1
Autor:
T.N. Oeltmann, S.W. Pelletier
Publikováno v:
Tetrahedron. 24(4)
A study of the NMR spectra of 44 diterpene alkaloids and derivatives is reported. A comparison of the NMR data for the C(4) Me group in a series of derivatives of atisine and veatchine provides support for the previous proposal regarding the conforma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c85a2f60df6f796dd96898a830fa5e2
https://pubmed.ncbi.nlm.nih.gov/5641820
https://pubmed.ncbi.nlm.nih.gov/5641820
Autor:
S.W. Pelletier, L.H. Keith
Publisher Summary This chapter introduces diterpene alkaloids. The diterpene alkaloids are derived from tetracyclic or pentacyclic diterpenes in which carbon atoms 19 and 20 are linked with the nitrogen of a molecule of β-aminoethanol, methylamine,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6d1c25b0d41ae950d78c99bd3bf1db4
https://doi.org/10.1016/s1876-0813(08)60099-8
https://doi.org/10.1016/s1876-0813(08)60099-8
Autor:
L.H. Keith, S.W. Pelletier
Publisher Summary This chapter discusses the chemistry of the C 20 -diterpene alkaloids. Many important developments have taken place. These include rigorous evidence for the presence of a bicyclo[2.2.2]-octane system in atisine, the correlation of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42959eceadadfbe456de7cefe23291a5
https://doi.org/10.1016/s1876-0813(08)60101-3
https://doi.org/10.1016/s1876-0813(08)60101-3