about
The Quest for Quinine: Those Who Won the Battles and Those Who Won the WarQuenching of pH-Responsive Luminescence of a Benzoindolizine Sensor by an Ultrafast Hydrogen ShiftThe Base-Promoted Rearrangements of Quaternary Ammonium SaltsCyclohexadiene ring opening observed with 13 fs resolution: coherent oscillations confirm the reaction path.Perchloropyracylene and its fusion with C60 by chlorine-assisted radio-frequency furnace synthesis.ORGANIC CHEMISTRY. Iron-catalyzed intermolecular [2+2] cycloadditions of unactivated alkenes.The activation strain model and molecular orbital theoryAnalysis of highly disfavored processes through pathway-specific correlated fluorescence.Controllable conversion of quasi-freestanding polymer chains to graphene nanoribbons.Pattern recognition analysis in complex molecule synthesis and the preparation of iso-Diels-Alder motifsExploiting [2+2] cycloaddition chemistry: achievements with allenes.Homogeneous photocatalytic reactions with organometallic and coordination compounds--perspectives for sustainable chemistry.Methods for activating and characterizing mechanically responsive polymers.125 years of chemistry in the mirror of "angewandte".Beyond click chemistry - supramolecular interactions of 1,2,3-triazoles.Allenes and computational chemistry: from bonding situations to reaction mechanisms.Cyclization reactions of bis(allenes) for the synthesis of polycarbo(hetero)cycles.How cyclobutanes are assembled in nature--insights from quantum chemistry.Recent progress in the chemistry of endohedral metallofullerenes.A novel oxy-oxonia(azonia)-cope reaction: serendipitous discovery and its application to the synthesis of macrocyclic musks.Cycloaddition of carbonyl compounds and alkynes to (di)silenes and (di)germenes: reactivity and mechanism.The Stone-Wales transformation: from fullerenes to graphite, from radiation damage to heat capacity.Studies in organic and physical photochemistry - an interdisciplinary approach.Photocleavage of coumarin dimers studied by femtosecond UV transient absorption spectroscopy.Asymmetric cycloaddition reactions catalysed by diarylprolinol silyl ethers.Carbon-Carbon Bond Formation in a Weak Ligand Field: Leveraging Open-Shell First-Row Transition-Metal Catalysts.Analyzing Reaction Rates with the Distortion/Interaction-Activation Strain Model.Catalytic Asymmetric Inverse-Electron-Demand Hetero-Diels-Alder Reactions.Cycloaddition Reactions: Why Is It So Challenging To Move from Six to Ten Electrons?The Effect of Pressure on Organic Reactions in Fluids-a New Theoretical Perspective.Activation of Dinitrogen as A Dipolarophile in 1,3-Dipolar Cycloadditions: A Theoretical Study Using Nitrile Imines as "Octet" 1,3-Dipoles.Reactive and unreactive pathways in a photochemical ring opening reaction from 2D femtosecond stimulated Raman.Organometallic chemistry: A new metathesis.A three-membered ring approach to carbonyl olefination.Mechanism of electrocyclic ring-opening of diphenyloxirane: 40 years after Woodward and Hoffmann.Thermal cyclization of phenylallenes that contain ortho-1,3-dioxolan-2-yl groups: new cascade reactions initiated by 1,5-hydride shifts of acetalic H atoms.Theoretical and experimental analysis of the reaction mechanism of MrTPS2, a triquinane-forming sesquiterpene synthase from chamomile.Mechanism of the forbidden [3s,5s]-sigmatropic shift: orbital symmetry influences stepwise mechanisms involving diradical intermediates.The Nozoe Autograph Books: Stories behind the Stories.Inducing and quantifying forbidden reactivity with single-molecule polymer mechanochemistry.
P2860
Q21032515-269D66E2-E324-4115-B5DA-91E1F0F776FBQ28821233-160C6ECF-D90D-4A24-933B-47124A63292BQ29392173-29CFFBAD-2A81-4B3C-B8C7-8C727904A624Q33392885-94C381E8-F4DF-4511-9702-108578A747C4Q34013968-843C58B2-140B-40CD-B26E-8AF870B6BD5FQ34491315-40A6786F-3734-4D99-AA29-7AE9236B437AQ34508508-CF6CE053-4440-43A9-B66A-158D35AEDF27Q36018015-D0DEED4F-BCB2-4640-AF3D-3D9BBAED4D07Q36305844-0D64907C-2635-4196-96AD-5B9A4B719766Q36990818-2955224E-CB4E-49F4-BA3A-300B11FA55D5Q37683513-39AEB63F-1012-4AB9-80AD-1A6624338279Q37979737-8725EAFD-1143-4EA4-99B1-DADCBCD7A847Q38079727-8FC1E468-E0DF-4F43-8E7B-4E99F2A0170DQ38082483-D022B441-8054-47BF-A273-9BC16ADC42EBQ38184880-35DB8302-2337-4B2B-B575-8B8D9BFB8A42Q38189659-775CED91-7348-43CC-9662-8E78338ACFE0Q38192915-90B51BC5-D0C4-4E10-B2B5-908D0D69073DQ38202882-ADC823BA-FB21-4A7E-84D3-706335694606Q38240159-DDF9DD88-FB08-4955-9EA5-49F8F2FE1E7FQ38261403-24A917AA-90E9-4E35-BAEC-140D0DACB074Q38579823-E8738093-4C67-4DA9-90B8-C0BE323C689AQ38833375-DEA5F984-0A18-408B-9372-C2B9DC34BAF1Q38887121-0D837B27-93C6-4077-B066-EDED8E6E9F23Q38997965-21AAFC31-BCA5-4D31-88B4-1CDF301D808CQ39018699-356CF14E-4287-4ABF-ABEF-AA731730C2E4Q39084109-DB9DEDC5-A399-4724-AD9F-63098E26C5E3Q39266241-D416BDEA-06C6-43F8-9C7E-D71FE52341ADQ39309202-90C948BA-AC65-4480-B87A-013E2631B2CBQ39400372-0F7EB34C-680D-4137-9981-D823D7A858A8Q39454654-BECEE60E-E134-4156-9E5A-27B51D67A317Q41094590-BC1202B0-9454-4688-A907-55FF2CC43CE1Q41245284-B9415D04-0DC0-41B2-8535-6F455F10B9BCQ42017305-9FF339EB-3F53-4CCD-8B12-04B3B193DA95Q42645943-D0DC195D-CB5D-468C-AEC0-6CAF4A4212AAQ43279316-D3AEA571-6524-492A-93FF-0FC1E99FAEA8Q43523759-16B69C37-B639-4C8E-BBAA-8BEED87FCDDDQ43654488-9C471778-262D-4CBE-918D-1A9BE716DEB7Q43938614-4A336826-8E4F-4252-A89A-371D978D4E0AQ43945562-9CAB628B-3A64-45C4-863A-297091145380Q44035015-9CAAEE28-BC42-4125-B301-59BB9C07F8CF
P2860
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована в листопаді 1969
@uk
name
The Conservation of Orbital Symmetry
@en
The Conservation of Orbital Symmetry
@nl
type
label
The Conservation of Orbital Symmetry
@en
The Conservation of Orbital Symmetry
@nl
prefLabel
The Conservation of Orbital Symmetry
@en
The Conservation of Orbital Symmetry
@nl
P356
P1476
The Conservation of Orbital Symmetry
@en
P2093
R. B. Woodward
P304
P356
10.1002/ANIE.196907811
P577
1969-11-01T00:00:00Z