Raw data for new compounds described in the paper: "Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations"
Description
Raw data for new compounds described in the paper: "Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations"
The enantioselective nickel-catalyzed desymmetrization of allenyl cyclohexa-2,5-dienones by reaction with arylboronic acids is described. Nickel-catalyzed arylation of the allene gives allylnickel species, which undergo cyclization by 1,4-allylation to produce hexahydroindol-5-ones and hexahydrofuran-5-ones with three contiguous stereocenters in high diastereo- and enantioselectivities.
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Related publication DOI
Subjects
- Chemicals
- Enantioselective catalysis
- Arylation
- Allenes
- Raw data for new compounds described in the paper: "Enantioselective nickel-catalyzed arylative intramolecular 1,4-allylations"
- Physical sciences::Chemistry::Organic chemistry::Organometallic chemistry
- Q Science::QD Chemistry::QD241 Organic chemistry
Divisions
- University of Nottingham, UK Campus::Faculty of Science::School of Chemistry
Deposit date
2018-05-14Data type
IR, NMR, mass spectrometry, and HPLC dataContributors
- Nguyen, Thi Le Nhon
- Incerti-Pradillos, Celia
- Lewis, William
Funders
- Other
- University of Nottingham
- GlaxoSmithKline
Data collection method
Using IR, NMR, and mass spectrometers, and HPLC machinesResource languages
- en