1 article(s) from Davis, Benjamin G
a) Variation of olefin metathesis: CM = cross-metathesis; RCM = ring-closing metathesis; ROM = ring...
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Allylic hydroxy activation in RCM .
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Possible complexes generated through preassociation of allylic alcohol with ruthenium.
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The influence of different OR groups on ring size-selectivity .
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Synthesis of palmerolide A precursors by Nicolaou et al. illustrates enhancement by an allylic hydr...
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a) Acceleration of ring-closing enyne metathesis by the allylic hydroxy group . b) Proposed mode of...
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a) Effect of the hydroxy group on the rate and steroselectivity of ROCM . b) Proposed H-bonded ruth...
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Plausible explanation for chemoselective CM of diene 16 .
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a) Efficient cross-metathesis of S-allylcysteine . b) Comparison of relative reactivity between all...
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a) Macrocycle synthesis by carbonyl-relayed RCM. b) Putative complex in carbonyl-relayed RCM .
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a) Sulfur assisted cross-metathesis . b) Putative unproductive chelates for larger ring sizes gener...
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Functionalization of Mukaiyama aldol product by CM in aqueous media .
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Comparison of reactivity between allyl sulfides and allyl selenides in aqueous cross-metathesis .
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Ring-closing metathesis on a protein .
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Expanded substrate scope of cross-metathesis on proteins .
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Beilstein J. Org. Chem. 2010, 6, 1219–1228, doi:10.3762/bjoc.6.140
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