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. 2017, 13, 2888–2894, doi:10.3762/bjoc.13.281
Graphical Abstract
Scheme 1: General reaction pathways for 3-aza-2-oxabicyclic alkenes.
Scheme 2: Various reactions involving modification of the alkene component of 3-aza-2-oxabicyclic alkenes.
Scheme 3: Various reactions involving cleavage of the C–O bond of 3-aza-2-oxabicyclic alkenes.
Scheme 4: Ring-opening reactions of cyclopropanated 3-aza-2-oxabicyclic alkenes.
Scheme 5: Different possible ring-opening pathways of cyclopropanated 3-aza-2-oxabicyclic alkenes.
Scheme 6: Possible mechanisms for the nucleophilic ring-opening of cyclopropanated 3-aza-2-oxabicyclic alkene ...
Beilstein J. Org. Chem. 2016, 12, 2189–2196, doi:10.3762/bjoc.12.209
Scheme 1: Various chemical transformations of 7-oxabenzonorbornadiene 1.
Scheme 2: Nucleophilic ring-opening reactions of 7-oxabenzonorbornadiene 1.
Scheme 3: Preparation of cyclopropanated 8 and its proposed ring-opening mechanisms.
Scheme 4: Formation of the possible regioisomers for the ring opening of asymmetric C1-substituted cyclopropa...
Beilstein J. Org. Chem. 2016, 12, 239–244, doi:10.3762/bjoc.12.25
Scheme 1: Palladium-catalyzed ring-opening reactions of oxabenzonorbornadiene.
Scheme 2: Palladium-catalyzed ring-opening of 1 with p-iodotoluene.
Scheme 3: Potential regioisomers from the palladium-catalyzed ring-opening reaction of 2 with aryl iodides.
Scheme 4: Palladium-catalyzed ring-opening of C1 substituted oxabenzonorbornadiene.
Scheme 5: Proposed mechanism for the palladium-catalyzed ring-opening reaction of oxanorbornadiene.