Relevant bibliographies by topics / Cis and trans-3-benzyl-2-phenyl-2

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Academic literature on the topic 'Cis and trans-3-benzyl-2-phenyl-2'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Cis and trans-3-benzyl-2-phenyl-2"

1

Falguni, Chattopadhyay, and K. Mallik Asok. "Schmidt reaction of trans-3-benzylflavanones : Formation of 3-benzyl-2- phenyl-2,3-dihydro-1,4-benzoxazepin-5(4H)ones having both cis and trans configurations." Journal of Indian Chemical Society Vol. 85, Oct 2008 (2008): 1057–59. https://doi.org/10.5281/zenodo.5820756.

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Department of Chemistry, Jadavpur University, Kolkata-700 032, India <em>E-mail</em> : mallikak52@yahoo.co. in <em>Manuscript received 5 May 2008, accepted 8 July 2008</em> On treatment with NaN<sub>3</sub>/c.H<sub>2</sub>SO<sub>4</sub>-HOA<sub>c</sub>, <em>trans</em>-3-benzylnavanones yield ring expansion products with alkyl migration and having either <em>cis</em> or both <em>cis</em> and <em>tran</em>s configurations.
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2

Van Betsbrugge, Jo, Wim Van Den Nest, Patricia Verheyden та Dirk Tourwé. "New amino acids derived from L-pyroglutamic acid: Synthesis of Trans-4-benzyl-cis-5-phenyl-L-proline, L-α-(2-benzyl-3-phenylpropyl)-glycine and L-α-(3-phenylpropyl)-glycine". Tetrahedron 54, № 9 (1998): 1753–62. http://dx.doi.org/10.1016/s0040-4020(97)10399-4.

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3

VAN BETSBRUGGE, J., W. VAN DEN NEST, P. VERHEYDEN та D. TOURWE. "ChemInform Abstract: New Amino Acids Derived from L-Pyroglutamic Acid: Synthesis of trans-4-Benzyl-cis-5-phenyl-L-proline, L-α-(2-Benzyl-3-phenylpropyl)-glycine and L-α-(3-Phenylpropyl)-glycine." ChemInform 29, № 25 (2010): no. http://dx.doi.org/10.1002/chin.199825235.

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4

Sofalvi, Szabolcs, Eric S. Lavins, Ian T. Brooker, et al. "Unique Structural/Stereo-Isomer and Isobar Analysis of Novel Fentanyl Analogues in Postmortem and DUID Whole Blood by UHPLC–MS-MS." Journal of Analytical Toxicology 43, no. 9 (2019): 673–87. http://dx.doi.org/10.1093/jat/bkz056.

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Abstract The presented analytical method enabled the Toxicology Department at the Cuyahoga County Medical Examiner’s Office to identify 26 and quantitatively report 24 compounds in 500 μL of whole blood, including fentanyl analogues (fentalogues) such as methoxyacetyl fentanyl (MeOAF) and cyclopropyl fentanyl (CPF). This second-generation method (FG2) was developed with the objective to improve the existing analysis (FG1) by decreasing sample size, lowering limits of detection (LOD) and lower limit of quantitation, minimizing ion suppression and resolving chromatographic interferences. Interfe
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5

F., G. BADDAR, N. BASYOUNI M., F. EI-NEWAIRY M. та H. GHALY E. "ᵧ.ᵧ-Disubstituted Itaconic Acids. Part Vll.1 The Stobbe Condensation of Benzyl-, p-Chlorobenzyl-, and p-Methoxybenzylphenyl Ketones with Diethyl Succinate". Journal of Indian Chemical Society Vol. 51, Jul 1974 (2022): 698–704. https://doi.org/10.5281/zenodo.6417065.

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Department of <em>Chemistry, </em>Faculty of Science, A&#39; in Shams <em>University, Cairo, Egypt.</em> <em>Manuscript received 22 October 1973 ; acepted 23 May 1974.</em> <em>\(Cis \)</em>(Ph/Ar)-5-Aryl-3-ethoxycarbonyl-4-phenyl-pent-4-enoic acids were converted into ethyl <em>\(trans\)-</em>(Ph/Ar)<em><sup>-</sup> 5-aryl-3-</em>carboxy-4-phenyl-pent-4-enoute (14), (15) and (16), which have been cyclised<em> </em>to 1-acetoxy-naphthalenes (17), (18) <em>and </em>(19). <em>\(Cis\) </em>(Ph/ Ar)<em>-4, </em>5-Diphenyl- <em>and </em>cis (Ph/Ar)-4-phenyl-5-p-tolyl-pent-4-enoic acid anhydrides<em
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6

Sreenivas, Kukkamudi, Chintada Nageswara Rao, and Faiz Ahmed Khan. "Intramolecular CH‐Hydrogen Bonding During the Dissociation of the Oxaphosphetane Intermediate Facilitates Z/E‐Selectivity in Wittig Olefination." ChemistryOpen, December 7, 2023. http://dx.doi.org/10.1002/open.202300171.

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AbstractHerein, DFT studies corroborating experimental results revealed that the shortest intramolecular hydrogen bonding distance of cis/trans‐oxaphosphetane (OPA) oxygen with the CH‐hydrogen of a triphenylphosphine phenyl ring provides good evidence for the attained olefin Z/E‐selectivity in Wittig olefination of the studied examples. 2‐Nitrobenzaldehyde, 3‐nitrobenzaldehyde, 2‐nitro‐3‐bromobenzaldehyde, 2‐nitro‐5‐bromobenzaldehyde and 2‐nitro‐5‐arylbenzaldehydes provided Z‐nitrostilbenes with (2‐chloro‐4‐hydroxy‐3‐methoxy‐5‐(methoxycarbonyl)benzyl) triphenylphosphonium chloride as the major
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7

Chattopadhyay, Falguni, and Asok K. Mallik. "ChemInform Abstract: Schmidt Reaction of trans-3-Benzylflavanones: Formation of 3-Benzyl-2-phenyl-2,3-dihydro-1,4-benzoxazepin-5(4H)ones Having Both cis and trans Configurations." ChemInform 40, no. 19 (2009). http://dx.doi.org/10.1002/chin.200919165.

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