Detalhe da pesquisa
1.
Synthesis of Cationic Biphen[4, 5]arenes as Biofilm Disruptors.
Angew Chem Int Ed Engl
; 62(21): e202301857, 2023 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36929684
2.
One-Pot and Shape-Controlled Synthesis of Organic Cages.
Angew Chem Int Ed Engl
; 60(33): 17904-17909, 2021 Aug 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34036741
3.
Complexation of an Antimicrobial Peptide by Large-Sized Macrocycles for Decreasing Hemolysis and Improving Stability.
Angew Chem Int Ed Engl
; 60(20): 11288-11293, 2021 05 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33709627
4.
Multiple Stimuli-Responsive Conformational Exchanges of Biphen[3]arene Macrocycle.
Molecules
; 25(24)2020 Dec 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33302382
5.
Unidirectional complexation of pillar[4]arene[1]benzoquinoneoxime with alkyl alcohols.
Org Biomol Chem
; 17(20): 4975-4978, 2019 05 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-31050343
6.
Efficient Separation of cis- and trans-1,2-Dichloroethene Isomers by Adaptive Biphen[3]arene Crystals.
Angew Chem Int Ed Engl
; 58(30): 10281-10284, 2019 Jul 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-31112359
7.
Terphen[n]arenes and Quaterphen[n]arenes (n=3-6): One-Pot Synthesis, Self-Assembly into Supramolecular Gels, and Iodine Capture.
Angew Chem Int Ed Engl
; 58(12): 3885-3889, 2019 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30600896
8.
Bis- and mono(m-benzoic acid)-functionalized pillar[5]arenes.
Org Biomol Chem
; 15(22): 4897-4900, 2017 Jun 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28540372
9.
Isocyanide-Based Multicomponent Bicyclization with Substituted Allenoate and Isatin: Synthesis of Unusual Spirooxindole Containing [5.5]-Fused Heterocycle.
J Org Chem
; 81(19): 9158-9166, 2016 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27653940
10.
Ugi/Himbert Arene/Allene Diels-Alder Cycloaddition to Synthesize Strained Polycyclic Skeleton.
J Org Chem
; 80(21): 11100-7, 2015 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26457659
11.
Isocyanide-based multicomponent reactions: concise synthesis of spirocyclic oxindoles with molecular complexity by using a [1,5]-hydrogen shift as the key step.
Chemistry
; 20(20): 5905-9, 2014 May 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-24700458
12.
AlCl3-promoted selective Michael addition with allenoate and methyleneindolinone: synthesis of spirocyclic oxindole by using allenoate as a four-carbon component building block.
J Org Chem
; 79(22): 11161-9, 2014 Nov 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-25347308
13.
Supramolecular Polymers Based on Efficient Pillar[5]arene-Neutral Guest Motifs.
Chemistry
; 19(36): 11892-7, 2013 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23922310
14.
A neutral supramolecular hyperbranched polymer fabricated from an AB2 -type copillar[5]arene.
Macromol Rapid Commun
; 34(23-24): 1856-62, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24285568
15.
Multicomponent reaction to construct spirocyclic oxindoles with a Michael (triple Michael)/cyclization cascade sequence as the key step.
Chemistry
; 18(31): 9645-50, 2012 Jul 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-22815218
16.
Complexation of neutral 1,4-dihalobutanes with simple pillar[5]arenes that is dominated by dispersion forces.
Org Biomol Chem
; 10(17): 3393-7, 2012 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-22441333
17.
Cascade reaction of o-enoyl arylisocyanide and o-hydroxy aromatic aldimine: diastereoselective access to a polycyclic spirobenzoxazine chromeno[4,3-b]pyrrole derivative.
Chem Commun (Camb)
; 58(75): 10528-10531, 2022 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36043872
18.
Complexation of 1,4-bis(pyridinium)butanes by negatively charged carboxylatopillar[5]arene.
J Org Chem
; 76(20): 8458-65, 2011 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-21923191
19.
Complex interactions of pillar[5]arene with paraquats and bis(pyridinium) derivatives.
Org Biomol Chem
; 8(7): 1568-76, 2010 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-20336850
20.
Palladium-catalyzed cascade reactions of enynones and isocyanides: access towards functionalized ketenimine and its application.
Chem Commun (Camb)
; 56(33): 4555-4558, 2020 Apr 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32202582