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Wiley Interdisciplinary Reviews-Computational Molecular Science, ISSN 1759-0876, 2015, Volume 5, Issue 4, pp. 324 - 343
Journal Article
Journal Article
Journal of Molecular Structure, ISSN 0022-2860, 10/2015, Volume 1098, pp. 72 - 75
The reaction between 2,3-dimethyl-1,3-butadiene and dimethyl 7-oxabicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate is efficiently achieved with small amounts of... 
Diels–Alder addition | Cyclohexadiene | Substituted benzene | retro-Diels–Alder reaction | retro-Diels-Alder reaction | Diels-Alder addition | CHEMISTRY, PHYSICAL | Cyclodextrins | Furans | Diels-Alder reaction | Butadiene | Analysis
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2010, Volume 49, Issue 48, pp. 9266 - 9269
Through oxidative carbene catalysis the reactivity of enals can be reversed at the β position from the typical electrophilic to nucleophilic (homoenolate... 
Michael addition | carbenes | redox activation | stereoselectivity | umpolung | ASYMMETRIC CATALYSIS | DIELS-ALDER REACTIONS | ORGANOCATALYSIS | N-HETEROCYCLIC CARBENES | CLAVULANIC ACID | CHEMISTRY, MULTIDISCIPLINARY | GAMMA-BUTYROLACTONES | ENANTIOSELECTIVE MICHAEL | ESTERS | CONJUGATE ADDITION
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 01/2014, Volume 20, Issue 4, pp. 1066 - 1072
Journal Article
Organic Letters, ISSN 1523-7060, 06/2019, Volume 21, Issue 11, pp. 4388 - 4391
An umpolung alpha-(hetero)arylation strategy that involves the Michael-type reaction between electron-rich (hetero)aromatic substrates and azoalkenes is... 
MILD | KETONES | DIELS-ALDER | CHEMISTRY, ORGANIC | CATALYZED ALPHA-ARYLATION | GRIGNARD-REAGENTS | INDOLES | C-H
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 11/2019, Volume 25, Issue 64, pp. 14694 - 14700
Boron compounds having a conjugated chelate backbone (N,C‐chelate or C,C‐chelate) and two mesityl substituents on boron have been found to undergo a facile... 
Diels–Alder addition | photoisomerization | boriranes | synthetic methods | arene ligands | dearomatization | TRANSFORMATION | ACTIVATION | RING EXPANSION | BENZENE | C BOND FORMATION | CHEMISTRY, MULTIDISCIPLINARY | Diels-Alder addition | GENERATION | FACILE | Photochemicals | Boron | Transformation | Boron compounds | Aromatic compounds | Chelates
Journal Article
Nature Communications, ISSN 2041-1723, 04/2017, Volume 8, Issue 1, p. 14875
Chiral metal catalysts have been widely applied to asymmetric transformations. However, the electronic structure of the catalyst and how it contributes to the... 
CHARGE-DENSITY | CHIRAL OXAZABOROLIDINES | DIELS-ALDER REACTIONS | NITRONES | HYDROGEN-BOND | 1,3-DICARBONYL COMPOUNDS | MULTIDISCIPLINARY SCIENCES | KETENE ACETALS | DIFFRACTION DATA | MICHAEL ADDITIONS | ENANTIOSELECTIVE 1,3-DIPOLAR CYCLOADDITION
Journal Article
Polymer, ISSN 0032-3861, 06/2018, Volume 145, pp. 157 - 161
Thermoresponsive copoly(β-thioether ester)s were efficiently synthesized from 2,5-furan diacrylate (2,5-FDA) via the thiol-Michael addition reaction under mild... 
Diels-Alder reaction | Renewable resources | Thiol-Michael | Thermoresponsive | DIELS-ALDER | POLYMER SCIENCE | MOLECULAR-WEIGHT | POLYMERIZATION | RELEASE | TEMPERATURE | BONDS | CHEMISTRY | LCST | EFFICIENT | POLY(N-ISOPROPYLACRYLAMIDE) | Thermal properties | Furans | Thiols | Polymer industry | Analysis
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 09/2018, Volume 83, Issue 17, pp. 10281 - 10288
Trisulfur radical anion (S3 •–) mediated reactions with in situ formed azoalkenes and α,β-usaturated N-sulfonylimines for the construction of... 
SITU GENERATED 1,2-DIAZA-1,3-DIENES | REDUCTIVE CLEAVAGE | DIELS-ALDER REACTION | CHEMISTRY, ORGANIC | AZOALKENES | CATALYTIC ASYMMETRIC-SYNTHESIS | SECONDARY-AMINES | 4+1 ANNULATION | AZIDE-FREE CONDITIONS | METAL-FREE | N-TOSYLHYDRAZONES
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2014, Volume 53, Issue 36, pp. 9512 - 9516
A remarkable fluorine effect on “on water” reactions is reported. The CF⋅⋅⋅HO interactions between suitably fluorinated nucleophiles and the hydrogen‐bond... 
heterogeneous catalysis | water chemistry | heterocycles | synthetic methods | fluorine | MUKAIYAMA-ALDOL | DIELS-ALDER | ASYMMETRIC-SYNTHESIS | ONE-POT SYNTHESIS | PROMOTED ORGANIC-REACTIONS | CHEMISTRY, MULTIDISCIPLINARY | ACCELERATION | ALCOHOLS | CARBONYL | CHEMISTRY | SILYL | Heterogeneous catalysis | Fluorides | Ketones | Aldehydes | Hydrogen | Green technology | Networks | Activated | Catalysts | Fluorine | Phase boundaries | Droplets | Nucleophiles | Fluorination
Journal Article