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256: Highly stereoselective synthesis of cyclopentanes bearing four stereocentres by a rhodium carbene-initiated domino sequence

August 1, 2014July 12, 2018 Davies Group

Authors: Brendan T Parr & Huw M.L. Davies

Nature Communications

5, Article number: 4455

256

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255: Mild Aminoacylation of Indoles and Pyrroles through Three-component Reaction with Ynol Ethers and Sulfonyl Azides
257: Synthesis of Complex Hexacyclic Compounds via a Tandem Rh(II)-Catalyzed Double-Cyclopropanation/Cope Rearrangement/Diels–Alder Reaction
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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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