Sign Up to like & get
recommendations!
0
Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b02439
Abstract: Axially chiral 1,3-disubstituted allenes were synthesized via hydroalkylation of alkyl- or aryl-substituted conjugated enynes (readily prepared via a Sonogashira reaction) with pronucleophiles such as dimethyl malonate under the cocatalysis of DTBM-SEGPHOS-ligated palladium and lithium iodide.…
read more here.
Keywords:
disubstituted allenes;
lithium iodide;
conjugated enynes;
palladium lithium ... See more keywords
Sign Up to like & get
recommendations!
0
Published in 2019 at "ACS Catalysis"
DOI: 10.1021/acscatal.9b02080
Abstract: The highly enantioselective copper-catalyzed three-component boroacylation of 1,1-disubstituted allenes is reported by using a class of chiral ligands (WJ-Phos), delivering various functionalized organoboron compounds bearing an all-carbon stereocenter in moderate to good yields with high…
read more here.
Keywords:
boroacylation disubstituted;
synthesis phos;
design synthesis;
disubstituted allenes ... See more keywords
Sign Up to like & get
recommendations!
1
Published in 2022 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.2c10863
Abstract: The general enantioselective catalytic synthesis of axially chiral 1,3-disubstituted allenes from readily available racemic propargylic alcohol derivatives remains a long-standing challenge in organic synthesis. Here we report an efficient nickel-catalyzed asymmetric propargylic substitution reaction/Myers rearrangement…
read more here.
Keywords:
disubstituted allenes;
nickel catalyzed;
synthesis;
axially chiral ... See more keywords