Zobrazeno 1 - 10
of 617
pro vyhledávání: '"Benzilic acid"'
Publikováno v:
IUCrData, Vol 9, Iss 10, p x241039 (2024)
The title compound, C14H12O3, is an α-hydroxycarboxylic acid whose orthorhombic polymorph has been reported earlier [Qiu et al. (2007). Inorg. Chim. Acta, 360, 1819–1824]. The asymmetric unit contains two complete molecules. Classical hydrogen bon
Externí odkaz:
https://doaj.org/article/e130699bed1d48dfac01cc6ac5d17846
Akademický článek
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Autor:
N. P. Pranamya
Publikováno v:
International Journal for Research in Applied Science and Engineering Technology. 9:337-343
A novel amino acid ligand derived from Benzilic acid and Tyrosine and its Cr (II), Fe (III), Co (II) and Ni (II) transition metal complexes were synthesized. The structure elucidation of the ligand and its complexes were derived on the basis of vario
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2daebfd618aca8205b280726cca496ec
https://doi.org/10.22214/ijraset.2021.37345
https://doi.org/10.22214/ijraset.2021.37345
Publikováno v:
Catalysts; Volume 12; Issue 9; Pages: 935
The reactions of the titanium alkoxide [Ti(OR)4] (R = Me, nPr, iPr, tBu) with the acids 2,2′-Ph2C(X)(CO2H), where X = OH and NH2, i.e., benzilic acid (2,2′-diphenylglycolic acid, L1H2), and 2,2′-diphenylglycine (L2H3), have been investigated. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::776ceddd11f60c39371a76ded8e6a709
Autor:
Xiao-Song Xue, Kendall N. Houk, Alexander J. E. Novak, Shuming Chen, Cooper S. Jamieson, Dirk Trauner, Hong Zhang
Publikováno v:
Journal of the American Chemical Society. 143:6601-6608
Computational studies with ωB97X-D density functional theory of the mechanisms of the steps in Trauner's biomimetic synthesis of preuisolactone A have elaborated and refined mechanisms of several unique processes. An ambimodal transition state has b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b8a774e21f1535c091c1c746fd7f49a
https://doi.org/10.1021/jacs.1c01856
https://doi.org/10.1021/jacs.1c01856
Autor:
Peter Lorenz, Marek Bunse, Simon Sauer, Jürgen Conrad, Florian C. Stintzing, Dietmar R. Kammerer
Publikováno v:
Fermentation, Vol 5, Iss 2, p 42 (2019)
Microbial fermentation of plant extracts with Lactobacteria is an option to obtain microbiologically stable preparations, which may be applied in complementary medicine. We investigated the metabolic conversion of constituents from Mercurialis perenn
Externí odkaz:
https://doaj.org/article/663bfac9d39f42129d5e5097756418d4
Publikováno v:
Journal of the American Chemical Society. 143:2699-2704
We report the first enantioselective total syntheses of the hasubanan alkaloid (-)-metaphanine and the norhasubanan alkaloid (+)-stephadiamine. Key features of these syntheses include diastereoselective oxidative phenolic coupling reaction and subseq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9630cce9ce0e2a3cb5ebbda83227e11d
https://doi.org/10.1021/jacs.1c00047
https://doi.org/10.1021/jacs.1c00047
Publikováno v:
Journal of Research in Pharmacy. 25:305-317
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5589d3da3719e3588d8931e600389b7a
https://doi.org/10.29228/jrp.21
https://doi.org/10.29228/jrp.21
Autor:
Salim Mohammed, Fatin zuhair
Publikováno v:
مجلة التربية والعلم, Vol 26, Iss 5, Pp 233-239 (2013)
الملخص یتضمن البحث تحضیر مرکبات هیدرازونالبنزیلیک (4a-g)و(5a-f) من خلال تکاثف معوضاتالاسیتوفینون وکذلک معوضاتالبنزوفینون مع هیدرازید حامض ا
Externí odkaz:
https://doaj.org/article/672dcb96806e421a96a57874cd225e78
Publikováno v:
Journal of the American Chemical Society. 142:19868-19873
The first and asymmetric total synthesis of 4β-acetoxyprobotryane-9β,15α-diol, containing a rare and highly strained trans-fused bicyclo[3.3.0]octane ring system, has been achieved. The synthetically challenging [6-5-5] tricyclic ring system in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f719d0d1d818aa481d8781c237e2cbbc
https://doi.org/10.1021/jacs.0c10116
https://doi.org/10.1021/jacs.0c10116