Zobrazeno 1 - 10
of 182
pro vyhledávání: '"(+) podocarpic acid"'
Publikováno v:
Pest Management Science. 76:3003-3011
Background In the field, we observed that many white-backed planthoppers (Sogatella furcifera, WBPHs) stayed in the top region of rice plants exposed to direct sunshine. It was known that WBPHs frequently took flight when the ground temperature was a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::397d9a65b6db447b82e0a46c298c0b6b
https://doi.org/10.1002/ps.5846
https://doi.org/10.1002/ps.5846
Autor:
Steven A. Li, Melissa M. Cadelis, Rebecca C. Deed, Hana Douafer, Marie-Lise Bourguet-Kondracki, Jean Michel Brunel, Brent R. Copp
Publikováno v:
Bioorganic & Medicinal Chemistry Letters
Bioorganic & Medicinal Chemistry Letters, 2022, 64, pp.116762. ⟨10.1016/j.bmc.2022.116762⟩
Bioorganic & Medicinal Chemistry Letters, 2022, 64, pp.116762. ⟨10.1016/j.bmc.2022.116762⟩
International audience; As part of our search for new antimicrobials and antibiotic adjuvants, a series of podocarpic acid-polyamine conjugates have been synthesized. The library of compounds made use of the phenolic and carboxylic acid moieties of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de36a59995610dcf390ebad6122e4001
https://doi.org/10.1016/j.bmc.2022.116762
https://doi.org/10.1016/j.bmc.2022.116762
Akademický článek
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Publikováno v:
Molecules, Vol 21, Iss 9, p 1197 (2016)
In this review the synthetic work in the field of aphidicolane, stemodane and stemarane diterpenoids, in which readily available (+)-podocarpic acid (4) was used as chiral template for the construction of their polycyclic structures, is described as
Externí odkaz:
https://doaj.org/article/64325944da1a4dc38f543d416ec224c1
Publikováno v:
European Journal of Organic Chemistry. 2018:1730-1734
A Suzuki-Miyaura coupling reaction of ortho-hydroxy-aromatic bromide 8 with isopropenylboronic acid pinacol ester has been investigated. It was found that the catalyst of Pd-2(dba)(3)/PCy3 in dioxa ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a11b058433bad6fe9def24752468911f
https://doi.org/10.1002/ejoc.201800070
https://doi.org/10.1002/ejoc.201800070
A growing molecular and structural understanding of the vitamin D receptor (VDR) ligand-binding pocket and the need for new pharmacological agents targeting vitamin D-related disease states has led to the identification of several classes of nonsecos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24458ca33e15cc0a4fdceb9a91e2e39e
https://doi.org/10.1016/b978-0-12-809963-6.00087-0
https://doi.org/10.1016/b978-0-12-809963-6.00087-0
Akademický článek
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Publikováno v:
Molecules, Vol 21, Iss 9, p 1197 (2016)
Molecules
Molecules
In this review the synthetic work in the field of aphidicolane, stemodane and stemarane diterpenoids, in which readily available (+)-podocarpic acid (4) was used as chiral template for the construction of their polycyclic structures, is described as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::571c5cc00ae4abb8e942292cb49f1263
http://www.mdpi.com/1420-3049/21/9/1197
http://www.mdpi.com/1420-3049/21/9/1197
Autor:
Rinaldo Marini Bettolo, Doriano Lamba, Francesca Leonelli, Luisa Maria Migneco, Azzurra Mostarda, Luca De Angelis, Nicola Demitri, Francesca Ceccacci, Angela La Bella
Publikováno v:
Journal of natural products
79 (2016): 1155–1159. doi:10.1021/acs.jnatprod.5b00834
info:cnr-pdr/source/autori:Leonelli F.; Mostarda A.; De Angelis L.; Lamba D.; Demitri N.; La Bella A.; Ceccacci F.; Migneco L.M.; Marini Bettolo R./titolo:Proof of the Structure of the Stemodia chilensis Tetracyclic Diterpenoid (+)-19-Acetoxystemodan-12-ol by Synthesis from (+)-Podocarpic Acid: X-ray Structure Determination of a Key Intermediate/doi:10.1021%2Facs.jnatprod.5b00834/rivista:Journal of natural products (Print)/anno:2016/pagina_da:1155/pagina_a:1159/intervallo_pagine:1155–1159/volume:79
79 (2016): 1155–1159. doi:10.1021/acs.jnatprod.5b00834
info:cnr-pdr/source/autori:Leonelli F.; Mostarda A.; De Angelis L.; Lamba D.; Demitri N.; La Bella A.; Ceccacci F.; Migneco L.M.; Marini Bettolo R./titolo:Proof of the Structure of the Stemodia chilensis Tetracyclic Diterpenoid (+)-19-Acetoxystemodan-12-ol by Synthesis from (+)-Podocarpic Acid: X-ray Structure Determination of a Key Intermediate/doi:10.1021%2Facs.jnatprod.5b00834/rivista:Journal of natural products (Print)/anno:2016/pagina_da:1155/pagina_a:1159/intervallo_pagine:1155–1159/volume:79
The first synthesis of (+)-19-acetoxystemodan-12-ol (1), a stemodane diterpenoid isolated from Stemodia chilensis, is described. The structure was supported by an X-ray crystallographic analysis of intermediate (+)-9a, which confirmed the proposed st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c3ffd3dccd62e783c91863c19907858
http://hdl.handle.net/11573/872820
http://hdl.handle.net/11573/872820