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cyclopentene

110. Catalytic Asymmetric Synthesis of Highly Functionalized Cyclopentenes by a [3 + 2] Cycloaddition

July 7, 2001July 12, 2018 Davies Group Publications

Authors: Huw M. L. Davies , Bangping Xiang , Norman Kong , and Douglas G. Stafford J. Am. Chem. Soc., 2001, 123 (30), 7461–7462

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78. Asymmetric Synthesis of Cyclopentenes by [3 + 2] Annulations between Vinylcarbenoids and Vinyl Ethers

September 30, 1998July 12, 2018 Davies Group Publications

Authors: Huw M. L. Davies , Norman Kong , and Melvyn Rowen Churchill J. Org. Chem., 1998, 63 (19), 6586–6589

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29. Regioselective [3 + 2] annulations with rhodium(ii)-stabilized vinylcarbenoids

February 29, 1992July 12, 2018 Davies Group Publications

Authors: Huw M.L. Davies, Baibua Hu Tetrahedron Lett.,  1992, 33, 455-456

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Research Topics

7-membered ring aldol alkyne amines annulation carbenoid Catalyst Design chiral auxiliaries chiral ligand cocaine Cope-Rearrangement cycloaddition cyclopentene Cyclopropanation cyclopropenation C–H Functionalization C–H Functionalization/Cope-Rearrangement diazo Donor/Acceptor dopamine transporters DOSP furan heterocycles Immobilized indole inter-molecular intra-molecular Natural Product PTAD pyridine pyrrole Rhodium(II) ring expansion serotonin transporters silver tandem triazole tropane vinyl carbenoid vinylogous reactivity ylide Ylide Formation [3+2] [3+4] [4+3]
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