about
Conformational stable alleno-acetylenic cyclophanes bearing chiral axes.1,3-Diethynylallenes (DEAs): enantioselective synthesis, absolute configuration, and chiral induction in 1,1,4,4-tetracyanobuta-1,3-dienes (TCBDs).Shape-persistent chiral alleno-acetylenic macrocycles and cyclophanes by acetylenic scaffolding with 1,3-diethynylallenes.Diverse Chiral Scaffolds from Diethynylspiranes: All-Carbon Double Helices and Flexible Shape-Persistent Macrocycles.Opening access to new chiral macrocycles: from allenes to spiranes.A Covalent Organic Helical Cage with Remarkable Chiroptical Amplification.Intense Optical Activity from Three-Dimensional Chiral Ordering of Plasmonic NanoantennasFingers Crossed: Optical Activity of a Chiral Dimer of Plasmonic NanorodsFrom individual to collective chirality in metal nanoparticlesRegioselectivity in Tether-Directed Remote Functionalization - The Addition of a Cyclotriveratrylene-Based Trimalonate to C60 RevisitedChiroptical Symmetry Analysis: Exciton Chirality-Based Formulae to Understand the Chiroptical Responses of and Symmetric SystemsAmplification of Chirality in Monodisperse, Enantiopure Alleno-Acetylenic OligomersEnantiomerically Pure Alleno-Acetylenic Macrocycles: Synthesis, Solid-State Structures, Chiroptical Properties, and Electron Localization Function AnalysisPreparation and Characterization of a Halogen-Bonded Shape-Persistent Chiral Alleno-acetylenic Inclusion ComplexRotation-Locked 2,6-Pyrido-allenophanes: Characterization of all StereoisomersPreparation of 13C4-6-methyl anthranilic ester via a Diels-Alder-type process. an experimental and theoretical study to characterize an unexpected isotope exchangeChiral (2,5)pyrido[7(4)]allenoacetylenic cyclophanes: synthesis and characterizationMorphological self-assembly of enantiopure allenes for upstanding chiral architectures at interfacesDevice-Compatible Chiroptical Surfaces through Self-Assembly of Enantiopure AllenesDesign and synthesis of chiral spirobifluorenesChiroptical Sensing: A Conceptual IntroductionMetallaaromatic biaryl atropisomersSpirobifluorene Metallaaromatics
P50
Q38244463-0A168192-71E8-426B-AD16-86C315A30C46Q46290425-7F99820E-33A5-4896-B29D-BF549BF3C1A5Q46611550-41CFF0C5-23CF-423E-B101-59F67B409C1AQ47959003-DFCFBC86-74D6-4CE4-BA87-F985AEA1F567Q50180921-2B4E66EE-EA56-4BBA-A2D7-7CF0238F84BEQ53495969-27D03C5B-E183-4F02-BDE9-188101EFF3EAQ60156806-0247590A-BF6B-4E51-A633-59B3DE859174Q60205930-3853B481-3805-4571-AEBA-04F929D9072BQ60205935-E04A061D-CD64-4ADF-A38E-1A6274E4C151Q60246011-BC3CB19E-C787-40C1-BD85-CEE9E718598CQ61453156-DDF55777-73E7-462D-9237-3E6E878491AAQ62567915-040ADCCA-1F16-4B0C-AFC4-5C2A42EFEB01Q62567917-3694E86E-8CA9-46F9-84C1-8120BB40603BQ64167027-F88EA964-CDA7-4997-832A-B1E2AAAD5199Q64167028-15C5390C-D922-456A-A486-7BEE774F24E0Q81041395-1A251C69-DC9E-4527-A260-CFC4EA16A7DBQ83900312-6BC3175F-55E1-4588-8802-1EE39ABEE34AQ85825166-B55DCEE6-3442-4CEF-BBCC-137123F53AF7Q88090060-FA6F1130-AC7C-4C70-8463-2CFACA81FDFBQ89694220-4F0E4AFA-4B7B-4659-86E2-EB9EA9909B8FQ89719318-FF3AF2DA-0E48-499E-B770-225A58316B9BQ91411662-F4CD1993-37E3-43E4-9728-58B0C9466D0DQ92727616-94434000-F343-4F0F-A46E-F6A5241C2399
P50
description
researcher ORCID ID = 0000-0002-6107-0120
@en
name
José Lorenzo Alonso-Gómez
@ast
José Lorenzo Alonso-Gómez
@en
José Lorenzo Alonso-Gómez
@es
José Lorenzo Alonso-Gómez
@nl
type
label
José Lorenzo Alonso-Gómez
@ast
José Lorenzo Alonso-Gómez
@en
José Lorenzo Alonso-Gómez
@es
José Lorenzo Alonso-Gómez
@nl
prefLabel
José Lorenzo Alonso-Gómez
@ast
José Lorenzo Alonso-Gómez
@en
José Lorenzo Alonso-Gómez
@es
José Lorenzo Alonso-Gómez
@nl
P1153
8649231000
P21
P31
P496
0000-0002-6107-0120