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A new approach to the nazarov reaction via sequential electrocyclic ring opening and ring closure.
J Am Chem Soc. 2006 Jul 26;128(29):9348-9. doi: 10.1021/ja063421a.
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An improved chiral auxiliary for the allene ether version of the Nazarov cyclization.
Org Lett. 2006 Jun 8;8(12):2579-82. doi: 10.1021/ol060816q.
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Tandem Nazarov cyclization-michael addition sequence catalyzed by an Ir(III) complex.
J Am Chem Soc. 2006 Apr 26;128(16):5312-3. doi: 10.1021/ja058772o.
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Stereoselective C-glycosylation reactions of pyranoses: the conformational preference and reactions of the mannosyl cation.
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Investigations into the role of ion pairing in reactions of heteroatom-substituted cyclic oxocarbenium ions.
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Enantioselective Nazarov reactions through catalytic asymmetric proton transfer.
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Stereochemistry of nucleophilic substitution reactions depending upon substituent: evidence for electrostatic stabilization of pseudoaxial conformers of oxocarbenium ions by heteroatom substituents.
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Cationic cyclopentannelation of allene ethers.
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Asymmetric cyclopentannelation: camphor-derived auxiliary.
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Synthesis and absolute stereochemistry of roseophilin.
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