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

July 7, 2001July 12, 2018 Davies Group

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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Publications cycloaddition, cyclopentene, Donor/Acceptor, DOSP, Rhodium(II), [3+2]. permalink.

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109. Kinetic Resolution and Double Stereodifferentiation in Catalytic Asymmetric C−H Activation of 2-Substituted Pyrrolidines
111. Catalytic Asymmetric Cyclopropanation of Heteroaryldiazoacetates
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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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