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Angewandte Chemie International Edition, ISSN 1433-7851, 10/2018, Volume 57, Issue 43, pp. 14235 - 14239
A synthetic method to prepare bicyclo[6.3.0]undeca‐2,4,9,trienyl esters efficiently from gold(I)‐catalyzed Rautenstrauch rearrangement/1,5‐hydride... 
cyclizations | gold | homogenous catalysis | synthetic methods | alkynes | PLATINUM | 2-CYCLOPENTENONES | MOLECULAR COMPLEXITY | CHEMISTRY, MULTIDISCIPLINARY | MEDIUM-SIZED RINGS | GOLD(I)-CATALYZED RAUTENSTRAUCH REARRANGEMENT | 8-MEMBERED CARBOCYCLES | DIELS-ALDER REACTION | CONSTRUCTION | CYCLIC ETHERS | CYCLIZATION | Esters | Catalysis | Gold | Organic chemistry | Isomerization
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2015, Volume 54, Issue 51, pp. 15511 - 15515
An enantio‐, diastereo‐, regio‐, and chemoselective phosphine‐catalyzed β,γ‐umpolung domino reaction of allenic esters with dienones has been developed for the... 
organocatalysis | phosphines | allenes | annulations | umpolung | C,N-CYCLIC AZOMETHINE IMINES | ENANTIOSELECTIVE 4+1 ANNULATIONS | HILIMAN REACTION | BAYLIS-HILLMAN REACTION | CHEMISTRY, MULTIDISCIPLINARY | EFFICIENT METHOD | SEQUENTIAL 2+3 | ASYMMETRIC 3+2 CYCLOADDITION | RAUHUT-CURRIER REACTION | GAMMA-SUBSTITUENT ALLENOATES | ELECTRON-DEFICIENT OLEFINS
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2017, Volume 56, Issue 38, pp. 11584 - 11588
Reported herein is an efficient copper(I)‐catalytic system for the diastereo‐ and enantioselective 1,2‐addition of 1,1‐bis[(pinacolato)boryl]alkanes to... 
enantioselectivity | amines | copper | diastereoselectivity | boron | ROOM-TEMPERATURE | CATALYZED NUCLEOPHILIC ALLYLATION | ASYMMETRIC-SYNTHESIS | AMINOBORATION | CHEMISTRY, MULTIDISCIPLINARY | TERTIARY BORONIC ESTERS | FACILE SYNTHESIS | DIBORYLMETHANE | VINYL HALIDES | ALLYLIC SUBSTITUTION | CYCLIC IMINES
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 08/2012, Volume 18, Issue 33, pp. 10362 - 10367
The degree of CC bond activation in the asymmetric bioreduction of α,β‐unsaturated carboxylic esters by ene‐reductases was studied, and general... 
ene‐reductase | enzymes | substrate activation | substituent effects | biocatalysis | ene-reductase | CYCLIC ENONES | TRANSFER HYDROGENATION | ENOATE REDUCTASES | ALDEHYDES | CHEMISTRY, MULTIDISCIPLINARY | OLD YELLOW ENZYME | ACID-DERIVATIVES |