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Code Context

<?php      */

<?php     function searchResults($p_get) {

<?php             $this->fulltextsearch = $p_get['fulltextsearch'];

SearchComponent::searchResults() - APP/Controller/Component/SearchComponent.php, line 25
SearchesController::searchResults() - APP/Controller/SearchesController.php, line 84
ReflectionMethod::invokeArgs() - [internal], line ??
Controller::invokeAction() - CORE/Cake/Controller/Controller.php, line 500
Dispatcher::_invoke() - CORE/Cake/Routing/Dispatcher.php, line 193
Dispatcher::dispatch() - CORE/Cake/Routing/Dispatcher.php, line 167
[main] - APP/webroot/index.php, line 105

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Code Context

<?php             $this->controller->set('keyword', $keyword);

<?php             $this->controller->set('mainClassId', $searchIn);

<?php             $this->controller->set('mainClass', $this->controller->MoleculeClass->getPath($searchIn)[0]);

SearchComponent::searchResults() - APP/Controller/Component/SearchComponent.php, line 63
SearchesController::searchResults() - APP/Controller/SearchesController.php, line 84
ReflectionMethod::invokeArgs() - [internal], line ??
Controller::invokeAction() - CORE/Cake/Controller/Controller.php, line 500
Dispatcher::_invoke() - CORE/Cake/Routing/Dispatcher.php, line 193
Dispatcher::dispatch() - CORE/Cake/Routing/Dispatcher.php, line 167
[main] - APP/webroot/index.php, line 105

Search

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Solvent

N/E-Parameter Range

Keyword

Exact search

29 | 30 | 31 | 32 | 33 | 34 | 35 | 36 | 37« Back Forward »Found 1683 molecules, page 33 of 85

Results per page:10|50|100|all Export as XLS

Name	Solvent	Reactivity Parameters	Reference (title or year)
(3-Cl)-tritylium ion		E Param.: 1.06	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(3-CF3)-tritylium ion		E Param.: 1.18	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-Me)-tritylium ion		E Param.: -0.13	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-Me)2-tritylium ion		E Param.: -0.70	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-Me)3-tritylium ion		E Param.: -1.21	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-MeO,3-OMe)-tritylium ion		E Param.: -1.62	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-OMe,3-Me)-tritylium ion		E Param.: -1.84	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-MeO,4-Me)-tritylium ion		E Param.: -2.13	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-MeO)2-tritylium ion		E Param.: -3.04	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-MeO)3-tritylium ion		E Param.: -4.35	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-NMe2)-tritylium ion		E Param.: -7.93	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-NMe2)2-tritylium ion (= Malachite green)		E Param.: -10.29	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(4-NMe2)3-tritylium ion (= Crystal violet)		E Param.: -11.26	J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y
(E)-3-(4-nitro-phenyl)-1-phenyl-prop-2-en-1-one (in DMSO)	DMSO	E Param.: -17.33	J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m
(E)-3-(4-cyano-phenyl)-1-phenyl-prop-2-en-1-one (in DMSO)	DMSO	E Param.: -17.64	J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m
(E)-1,3-diphenylprop-2-en-1-one (in DMSO)	DMSO	E Param.: -19.39	J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106
(E)-4-(4-nitrophenyl)but-3-en-2-one (in DSMO)	DMSO	E Param.: -19.36	J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m
(E)-4-methyl-1-(4-nitrophenyl)pent-1-en-3-one (in DMSO)	DMSO	E Param.: -19.17	J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m
(E)-4,4-dimethyl-1-(4-nitrophenyl)pent-1-en-3-one	DMSO	E Param.: -19.15	J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m
3-chloro-benzaldehyde (in DMSO)	DMSO		J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m

News

01/30/25:
Sesamol-derived ortho-quinone methides (o-QM) have been added (ChemEurJ 2024, e202403785 & OBC 2025, 23, 827-834)
05/22/24:
Lactone enolates have been added (JOC 2024, 89, 6915-6928).
11/13/24:
2-Methylene-1,2-dihydropyridines (2-pyNHOs) have been added (EurJOC 2024, 27, e202400373).
05/21/24:
Mesoionic pyridinium-derived N-heterocyclic olefins (py-mNHOs) have been added (Angew. Chem. Int. Ed. 2024, 63, e202318283).
10/19/23:
Enamines derived from 4-(alkylthio)-3-imidazolines and aldehydes have been added (ChemEurJ 2023, doi: 10.1002/chem.202302764).
09/28/23:
Mesoionic N-heterocyclic olefins (mNHOs) have been added (Angew. Chem. Int. Ed. 2023, 62, e202309790).
07/05/23:
S-Cyanomethylated imidazolidine-4-thione-derived enamines have been added (ChemComm 2023, 59, 8091).
03/16/23:
Cyclic alpha-diazo carbonyl compounds added (EurJOC 2023, 26, e202300005)
01/30/23:
NADH and NADPH reactivities (in water, pH 7) determined by Mayer and Moran have been added (OBC 2022, 21, 85-88).
09/20/22:
Alkenyl boronate nucleophilicity by Liu, Ready and co-workers has been added (JACS 2022, 144, 16118).
01/30/23:
Electrophilicities of diazo compounds in azo couplings (ChemEurJ 2022, 28, e202201376)
01/30/23:
Diazocyclopentadiene added (Synthesis 2023, 55, 354-358)
01/30/23:
Electrophilic indoles added (ChemCommun 2021, 57, 10071-10074)
04/13/21:
Cyclic Michael acceptors added (Chem. Sci. 2021, 12, 4850-4865)
05/21/21:
Thiophenolates (in DMSO) added (JOC 2021, 86, 5965-5972)
05/06/20:
Heteroallenes added (JACS 2020, 142, 8383-8402).
01/27/20:
Pyrrolidines and Imidazolidinones added (JACS 2020, 142, 1526-1547).
05/06/20:
GSH reactivity added (Angew. Chem. Int. Ed. 2019, 58, 17704-17708)
01/30/23:
Phenolates added (JOC 2019, 84, 8837-8858)
04/24/18:
Ketones added (JACS 2018, 140, 5500).
11/03/17:
Allyl-boron nucleophiles added (JACS 2017, 139, 15324)
04/23/18:
Peroxide anions added (Angew. Chem. Int. Ed. 2017, 56, 13279).
04/23/18:
Michael acceptors added (JACS 2017, 139, 13318).
06/16/17:
Nucleophilicities of VNS reagents (JOC 2017, 82, 1011).