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Chemical Communications: Chem Comm, ISSN 1359-7345, 2/2014, Volume 5, Issue 19, pp. 2393 - 248
Over the past few decades, the semipinacol rearrangement has been widely applied in the field of organic synthesis. However, its catalytic asymmetric version... 
Progressions | Synthesis | Catalysis | Asymmetry | Catalysts | Chemists
Journal Article
Chemical Communications, ISSN 1359-7345, 03/2014, Volume 50, Issue 19, pp. 2393 - 2408
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2017, Volume 56, Issue 5, pp. 1381 - 1384
A combination of Cp*RhIII‐catalyzed C−H activation and Wagner–Meerwein‐type rearrangement was successfully achieved for the first time. Thus, bridged... 
RhIII catalysis | Wagner–Meerwein rearrangement | C−H activation | azabicyclic alkenes | catalysis | Catalysis | Coupling (molecular) | Activation
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2013, Volume 52, Issue 15, pp. 4229 - 4234
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2017, Volume 56, Issue 21, pp. 5858 - 5861
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 12/2014, Volume 356, Issue 18, pp. 3749 - 3754
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2016, Volume 55, Issue 49, pp. 15411 - 15414
An enantioselective pinacol rearrangement of functionalized (E)‐2‐butene‐1,4‐diols was developed. In the presence of a catalytic amount of a chiral... 
1,4-diols | organocatalysis | pinacol rearrangements | ion pairs | chiral Brønsted acids | WAGNER-MEERWEIN REARRANGEMENT | BRONSTED ACID CATALYST | ASYMMETRIC CATALYSIS | RING EXPANSION | QUATERNARY STEREOCENTERS | CHEMISTRY, MULTIDISCIPLINARY | PROTONATION | 1 | PHOSPHORIC-ACID | 4-diols | SEMIPINACOL REARRANGEMENT | LIGNANS | chiral BrOnsted acids | DERIVATIVES | Enantiomers | Catalysis
Journal Article
Synlett, ISSN 0936-5214, 09/2011, Volume 22, Issue 14, pp. 2043 - 2047
Abstract A new catalyst system for the enantioselective bromine-induced semipinacol rearrangement of cyclic allylic alcohols is described. Using the... 
letter | bromine | electrophilic addition | halogenation | asymmetric catalysis | rearrangement | BRONSTED ACID | BROMOLACTONIZATION | COMPLEX | RING EXPANSION | CHEMISTRY, ORGANIC | PINACOL REARRANGEMENT | ALLYLIC ALCOHOLS | ENANTIOSELECTIVE HALOCYCLIZATION | HIGHLY EFFICIENT SYNTHESIS | WAGNER-MEERWEIN SHIFT | DERIVATIVES
Journal Article
Journal of Molecular Liquids, ISSN 0167-7322, 01/2018, Volume 249, pp. 949 - 952
Reaction of (3aRS,6SR,7aRS)-6-substituted 2-phenyl-2,3,7,7a-tetrahydro-3a,6-epoxyisoindol-1(6H)-ones (1–3) with ICl (or Br2) in CH2Cl2 yields to halogenated... 
Halogen bonding | 3a,6-epoxyisoindole | Hydrogen bonding | Wagner-Meerwein rearrangement | Halogenation | STEROIDAL 16,17-EPOXIDES | ORGANIC-SYNTHESIS | DESIGN | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | CHEMISTRY, PHYSICAL | Hydrogen | Pyridine
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2018, Volume 16, Issue 30, pp. 5441 - 5445
A straightforward two-step entry to -oxgenated ,-unsaturated ketones from readily available ,-unsaturated ketones is disclosed. It was found that bis(allylic)... 
MIGRATION | ALCOHOLS | INITIATED PINACOL REARRANGEMENT | RING EXPANSION | STEREOSELECTIVE CONSTRUCTION | ACID CATALYSIS | STEREOCHEMISTRY | SEMIPINACOL REARRANGEMENT | CHEMISTRY, ORGANIC | WAGNER-MEERWEIN SHIFT | DERIVATIVES
Journal Article
Tetrahedron, ISSN 0040-4020, 11/2014, Volume 70, Issue 44, pp. 8374 - 8379
The Wagner–Meerwein rearrangement of [3.3.1] bicyclic N-Boc aminols was established, featuring the migration of the vinyl group instead of the aromatic ring.... 
Wagner–Meerwein rearrangement | N-Boc aminol | Structure elucidation | Lycoposerramine R | 3.3.1 | Wagner-Meerwein rearrangement [3.3.1] | ALCOHOLS | (-)-HUPERZINE | SERRATININE | CARBOCATIONS | CHEMISTRY, ORGANIC | LYCOPODIUM ALKALOIDS | HUPERZINE-B | Tetrahedrons | Spectroscopy | Spectroscopic analysis | Aromatic compounds | Migration
Journal Article
Chemical Communications, ISSN 1359-7345, 05/2014, Volume 50, Issue 34, pp. 4445 - 4447
A method using quinidine and optically active binol-derived phosphoric acid as a cocatalyst to catalyze the asymmetric semipinacol rearrangement of... 
WAGNER-MEERWEIN REARRANGEMENT | RING EXPANSION | REAGENTS | 2-HALO-2-ALKENYL KETONES | ALKYLATION | CARBON QUATERNARY STEREOCENTERS | CONSTRUCTION | ALDEHYDES | ALLENOLS | CHEMISTRY, MULTIDISCIPLINARY | ALPHA-BRANCHED ENALS | Purity | Optical activity | Phosphoric acid | Forming | Asymmetry
Journal Article
Chemistry of Heterocyclic Compounds, ISSN 0009-3122, 9/2016, Volume 52, Issue 9, pp. 736 - 742
Journal Article