This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.
Beilstein J. Org. Chem. 2010, 6, No. 22, doi:10.3762/bjoc.6.22
Graphical Abstract
Scheme 1: Dearomatising cyclisations (a) of enolates; (b) of electron-rich heteroaromatics.
Scheme 2: Synthesis of ketone 7.
Scheme 3: Dearomatising cyclisation to a 5-benzoylhexahydroisoquinoline.
Scheme 4: Synthesis of ester 12.
Scheme 5: Dearomatising cyclisation of ester 12.
Figure 1: Coupling constants (Hz) in the major diastereoisomer of 15.
Scheme 6: Synthesis of esters 18.
Scheme 7: Dearomatising cyclisation to form tetrahydrofurans.
Figure 2: Determination of the stereochemistry of 20b. Arrows indicate nuclear Overhauser enhancements.