TY  - JOUR
A1  - Schmidt, Bernd
A1  - Nave, Stefan
T1  - Stereoselective syntheses of enantiomerically pure 2,5-disubstituted dihydropyrans based on olefin metathesis
JF  - The journal of organic chemistry
N2  - A short synthesis of 2,5-disubstituted dihydropyrans starting from D-mannitol as a chiral building block is described. Our synthetic approach combines ruthenium-catalyzed ring closing olefin metathesis and palladium-catalyzed nucleophilic substitution.
Y1  - 2006
U6  - https://doi.org/10.1021/jo061190k
SN  - 0022-3263
VL  - 71
IS  - 19
SP  - 7364
EP  - 7369
PB  - American Chemical Society
CY  - Washington
ER  - 
TY  - JOUR
A1  - Schmidt, Bernd
A1  - Nave, Stefan
T1  - Control of ring size selectivity by substrate directable RCM
N2  - Hydroxy groups may exert strong catalyst-directing effects in olefin metathesis reactions, which are exploited for a ring size-selective RCM reaction
Y1  - 2006
UR  - http://pubs.rsc.org/en/content/articlehtml/2006/cc/b604359c
U6  - https://doi.org/10.1039/B604359c
ER  - 
TY  - JOUR
A1  - Schmidt, Bernd
A1  - Nave, Stefan
T1  - Palladium-catalyzed O-allylation of alpha-hydroxy carbonyl compounds
N2  - alpha-Hydroxy carbonyl compounds undergo smooth O-allylation using allylic carbonates and Pd(0) catalysts. This method has significant advantages over other O-allylation methods as it provides a solution to several problems previously observed for this synthetic transformation
Y1  - 2006
UR  - http://onlinelibrary.wiley.com/doi/10.1002/adsc.200505361/pdf
U6  - https://doi.org/10.1002/adsc.200505361
ER  -