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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
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, 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
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2013, Volume 52, Issue 15, pp. 4229 - 4234
Journal Article
Zeitschrift für anorganische und allgemeine Chemie, ISSN 0044-2313, 01/2019, Volume 645, Issue 1, pp. 22 - 26
Using 1,1,2‐triphenylethane‐1,2‐diol, AgSbF6, and NOSbF6, two different carbonyl products of rearrangement were synthesized: neutral ketone compound... 
Silver | Wagner–Meerwein shift | Migratory aptitude | Pinacol rearrangement | MIGRATION | EPOXIDES | ELECTRON-TRANSFER | MEERWEIN REARRANGEMENT | SALTS | Wagner-Meerwein shift | CHEMISTRY, INORGANIC & NUCLEAR
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, 03/2017, Volume 73, Issue 13, pp. 1740 - 1744
Treatment of betulin-type saponins, in which the sugar moiety is connected at the 28-position, with TMSOTf affords 3-O-substituted allobetulin saponins. This... 
Saponins | Betulin | Synthesis | Allobetulin | The Wagner-Meerwein rearrangement | GLYCOSIDES | LUPANE-TYPE SAPONINS | CHEMISTRY, ORGANIC | GLYCOSYLATION | CYTOTOXICITY | GERMANICANE-TYPE | TRITERPENE
Journal Article