Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Jean Bruneton"'
Autor:
Pascal Richomme, Jean Bruneton, Denis Séraphin, Thierry Sévenet, Marc Litaudon, Anne-Emmanuelle Hay, Cécile Morel
Publikováno v:
Molecules, Vol 7, Iss 1, Pp 38-50 (2002)
An EtOAc extract of the stem bark of Calophyllum caledonicum (Clusiaceae) yielded thirteen new hydroxylated and/or prenylated xanthone derivatives, namely 5-hydroxy-8-methoxyxanthone (1), 3,5-dihydroxy-1,2-dimethoxyxanthone (2), 1,8-dihydroxy-6,7-dim
Externí odkaz:
https://doaj.org/article/48394325a29e4fdd88608faa19b1e177
Autor:
Anne-Emmanuelle Hay, Cécile Morel, Thierry Sevenet, Pascal Richomme, Jean Bruneton, Marc Litaudon, Denis Séraphin
Publikováno v:
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 7, Iss 1, Pp 38-50 (2002)
Molecules; Volume 7; Issue 1; Pages: 38-50
Molecules, Vol 7, Iss 1, Pp 38-50 (2002)
Molecules; Volume 7; Issue 1; Pages: 38-50
An EtOAc extract of the stem bark of Calophyllum caledonicum (Clusiaceae) yielded thirteen new hydroxylated and/or prenylated xanthone derivatives, namely 5- hydroxy-8-methoxyxanthone (1), 3,5-dihydroxy-1,2-dimethoxyxanthone (2), 1,8-dihydroxy- 6,7-d
Autor:
Denis Séraphin, Jean Bruneton, Pascal Richomme, Olivier Duval, Jean-Jacques Helesbeux, David Guilet
Publikováno v:
Tetrahedron Letters. 41:4559-4562
Photooxygenation (1O2) of ortho-prenylphenols followed by a reduction (PPh3) at low temperature (−30°C) yields a mixture of ortho-(2-hydroxy-3-methylbut-3-enyl)phenols and ortho-(3-hydroxy-3-methylbut-1-enyl)phenols. However, by running the two-st
Publikováno v:
ChemInform. 23
(R)-(+)-Noranicanine (1a), a new type of benzylisoquinoline precursor was isolated from Aniba canelilla (Lauraceae) and its structure was determined by means of spectroscopic data as well as by synthesis
Publikováno v:
ChemInform. 24
Autor:
Jean Bruneton, Pascal Richomme, Denis Séraphin, Jean-Jacques Helesbeux, David Guilet, Olivier Duval
Publikováno v:
ChemInform. 31
Photooxygenation (1O2) of ortho-prenylphenols followed by a reduction (PPh3) at low temperature (−30°C) yields a mixture of ortho-(2-hydroxy-3-methylbut-3-enyl)phenols and ortho-(3-hydroxy-3-methylbut-1-enyl)phenols. However, by running the two-st
Autor:
Abdelilah Benosman, Jean Bruneton, Thierry Sevenet, Pascal Richomme, Guillaume Perromat, A. Hamid A. Hadi
Publikováno v:
Phytochemistry. 40:1485-1487
A new tirucallane triterpene, (−)-leucophyllone, was isolated from the stem bark of Aglaia leucophylla and its structure was elucidated from spectral data as 23( Z )-25-methoxy-tirucall-7,23-diene-3-one. In addition, (−)-caryophyllene oxide, (−
Publikováno v:
Phytochemistry. 37:1143-1145
Bioactivity guided fractionation of an ethanolic extract of the stem bark of Aglaia leucophylla led to the isolation of two new 3,4-secotirucallane type triterpenoids, namely (24 Z )-3,4-secotirucalla-4(28),7,24-triene-3,26-dioic acid and its 3-monom
Autor:
Gérald Larcher, Jean Bruneton, Agnès Teyrouz, Jean-Philippe Bouchara, Cécile Morel, Pascal Richomme, Marc Litaudon, Denis Séraphin
Publikováno v:
Planta medica. 68(1)
Two new xanthones, namely caledonixanthones E (1) and F (2), were isolated from the stem bark of Calophyllum caledonicum (Guttiferae). The structural elucidation of these compounds was mainly established on the basis of 1D, 2D NMR and HRMS spectrosco
Publikováno v:
Phytochemistry. 58(4)
Six coumarins have been isolated from the fruits and the stem bark of Calophyllum dispar (Clusiaceae). The structures of these minor components were established by means of spectroscopic analysis, including extensive 2D NMR studies. Some of these cou