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ChemPhysChem, ISSN 1439-4235, 06/2017, Volume 18, Issue 11, pp. 1486 - 1489
Single‐molecule force spectroscopy (SMFS) of multi‐mechanophore polymers has been used to provide kinetic and mechanistic insights into mechanochemical... 
mechanochemistry | polymers | atomic force microscopy | electrocyclic reactions | kinetics | PATHWAYS | POLYMER MECHANOCHEMISTRY | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | CHEMISTRY, PHYSICAL | EXTENSION | MICROSCOPY | CYCLOBUTENE | HYDRODYNAMIC DRAG | DYNAMIC STRENGTH | BONDS | CHEMISTRY | Atomic force microscopy | Polymers | Spectrum analysis | Analysis
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 10/2016, Volume 81, Issue 19, pp. 8777 - 8788
Suprafacial sigmatropic shift reactions of 5-substituted cyclopentadienes, 3-substituted cyclopropenes, and 7-substituted cycloheptatrienes have been studied... 
CURRENT-DENSITY | HYDROGEN SHIFTS | CYCLOBUTENES | AB-INITIO | ISOMERIZATION | CHEMISTRY, ORGANIC | SYSTEMS | CONROTATORY ELECTROCYCLIC REACTIONS | MAGNETIC-PROPERTIES | CYCLOPENTADIENE | MOLECULES | Propylene | Chemical reactions | Usage | Chemical properties | Transition state (Chemistry) | Analysis
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 06/2015, Volume 56, Issue 24, pp. 3813 - 3815
[Display omitted] Recently we have shown that retro-Nazarov reactions are under the control of geminal bond participation. In retro-Nazarov reactions,... 
Bond model analysis | Torquoselectivity | Geminal bond participation | Retro-Nazarov reaction | CYCLOBUTENES | RING-OPENING REACTIONS | CHEMISTRY, ORGANIC | REACTIVITIES | SUBSTITUENT | CONROTATORY ELECTROCYCLIC REACTIONS | SILYL | ORBITAL PHASE THEORY | INWARD TORQUOSELECTIVITY
Journal Article
Synlett, ISSN 0936-5214, 04/2018, Volume 29, Issue 7, pp. 856 - 862
Journal Article
ChemPhysChem, ISSN 1439-4235, 01/2006, Volume 7, Issue 1, pp. 111 - 113
Journal Article
Helvetica Chimica Acta, ISSN 0018-019X, 06/2011, Volume 94, Issue 6, pp. 1053 - 1064
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 05/2017, Volume 82, Issue 9, pp. 4758 - 4765
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 11/2015, Volume 137, Issue 44, pp. 14063 - 14066
o-Alkylphenyl ketones undergo a C–C bond forming carboxylation reaction with CO2 simply upon irradiation with UV light or even solar light. The reaction... 
ORGANIC-SYNTHESIS | CATALYZED DIRECT CARBOXYLATION | DIELS-ALDER REACTIONS | HYDROCARBOXYLATION | ELECTROCYCLIC REACTIONS | MEDIATED CARBOXYLATION | TRANSITION-METAL CATALYSTS | CARBON-DIOXIDE | AROMATIC-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 02/2019, Volume 2019, Issue 5, pp. 957 - 968
Dendralenes are simple alkenes with cross‐conjugated double bonds that are frequently synthesized due to being potentially valuable building blocks for the... 
Alkenes | Cross‐coupling | Aluminum | C–C bond formation | Electrocyclic reactions | Cross-coupling | PALLADIUM | ONE-POT | CYCLOBUTENES | RING-OPENING REACTIONS | CHEMISTRY, ORGANIC | CROSS-COUPLING REACTIONS | DIENES | FACILE SYNTHESIS | C-C bond formation | DENDRALENE FAMILY | STEREOSELECTIVE-SYNTHESIS | SILYL SUBSTITUENT
Journal Article
Synthesis, ISSN 0039-7881, 09/2015, Volume 47, Issue 17, pp. 2545 - 2548
Abstract During synthetic studies toward bi-linderone, unexpected 6π-electrocyclizations of 4,5-dimethoxy-2-[( E... 
special topic | natural products | transition states | electrocyclic reactions | spiro compounds | alkene
Journal Article
by Xiao, FF and Zhang, Q and Wang, YX and Hu, XD
SYNTHESIS-STUTTGART, ISSN 0039-7881, 09/2015, Volume 47, Issue 17, pp. 2545 - 2548
During synthetic studies toward bi-linderone, unexpected 6-electrocyclizations of... 
natural products | ROUTE | LINDERASPIRONE | transition states | alkene | CHEMISTRY, ORGANIC | electrocyclic reactions | spiro compounds | ELECTROCYCLIZATIONS
Journal Article
ASIAN JOURNAL OF ORGANIC CHEMISTRY, ISSN 2193-5807, 10/2017, Volume 6, Issue 10, pp. 1415 - 1420
Acetate derivatives of 2-en-4-yne alcohols 1 and enyne oxiranes 4 regioselectively underwent 1,5-substitution (S(N)2 '') reactions with Grignard reagents in... 
regioselectivity | DIELS-ALDER REACTIONS | VINYL-ALLENES | CHEMISTRY, ORGANIC | CARBONYL-COMPOUNDS | ELECTROCYCLIC RING-CLOSURE | enynes | 4+1 CYCLOADDITION | KETONES | Grignard reaction | CROSS-COUPLING REACTIONS | nucleophilic substitution | VINYLALLENES | ESTERS | iron | STEREOSELECTIVE-SYNTHESIS
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 2008, Volume 49, Issue 23, pp. 3725 - 3728
The total synthesis of the 2-azaanthraquinone alkaloid, scorpinone ( 4), isolated from the mycelium of a Bispora-like tropical fungus, has been completed in... 
Microwave | Electrocyclic reaction | [4+2] Cycloaddition | 2-Azaanthraquinone | Scorpinone | THERMAL ELECTROCYCLIC REACTION | ANTIBIOTICS | scorpinone | 2-azaanthraquinone | CHEMISTRY, ORGANIC | electrocyclic reaction | 6-DEOXYBOSTRYCOIDIN | DERIVATIVES | microwave | [4+2] cycloaddition | AZAANTHRAQUINONE
Journal Article
Tetrahedron, ISSN 0040-4020, 06/2013, Volume 69, Issue 23, pp. 4546 - 4551
The Rh2(OAc)4-catalyzed reaction of 2H-azirine-2-carbaldehydes with dimethyl diazomalonate proceeds via azirinium ylide formation, isomerization to... 
Diazo compounds | Carbenoids | Azirines | Ylides | Electrocyclic reactions
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2014, Volume 53, Issue 50, pp. 13740 - 13745
A rare example of a one‐pot process that involves asymmetric triple relay catalysis is reported. The key step is an asymmetric [1,5] electrocyclic reaction of... 
tandem reaction | thioureas | asymmetric catalysis | electrocyclic reactions | one‐pot processes | Tandem reaction | Thioureas | One-pot processes | Asymmetric catalysis | Electrocyclic reactions
Journal Article