3 article(s) from Ahmed, Faiz
Examples of the reductive iodonio-Claisen rearrangement compared to new reactivity seen with benzyl...
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Crossover reaction experiments.
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Suggested mechanism based on product formation and crossover experiments.
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Proposed mechanism for the generation of 2i from Table 2, entry 8.
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Beilstein J. Org. Chem. 2018, 14, 1039–1045, doi:10.3762/bjoc.14.91
Synthesis of Nortricyclenes from Norbornenes.
X-ray crystal structure of 5a with 30% thermal ellipsoids.
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KO2-mediated synthesis of tetrachloro-substituted 3-methylenenortricyclenes. Reaction conditions: A...
Plausible mechanism of the KO2-mediated reaction.
X-ray crystal structure of 8a with 30% thermal ellipsoids.
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Plausible mechanism of the acylation reaction of 3-methylenenortricyclenes.
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Beilstein J. Org. Chem. 2014, 10, 2531–2538, doi:10.3762/bjoc.10.264
Diels–Alder bis-adducts of 1 with cyclic dienes.
Diels–Alder reaction of 1a with 3-sulfolene.
Synthesis of bis-oxa-bridged compounds 8 and 10 from bis-adducts 5 and 6.
ORTEP structure of 8 [50% probability thermal ellipsoids; some of the hydrogen atoms and a solvent ...
Diels–Alder reaction of 1b with 3-sulfolene.
Synthesis of bis-oxa-bridged compounds 8 and 10 from bis-diketones 14 and 15.
1H NMR chemical shifts (in parentheses) and coupling constants (J) for the three interacting proton...
Transition state models for the bis-adduct formation.
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Beilstein J. Org. Chem. 2010, 6, No. 64, doi:10.3762/bjoc.6.64
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