Modulation of π-facial selectivities in nucleophilic additions to 7-norbornenones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
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3. Reactions of norbornen-7-one with Grignard reagents
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5. Nucleophilic addition of the pentafluoroethyl group to aldehydes, ketones, and esters
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1. Synthesis of 7-norbornenols via Diels–Alder cycloadditions of cyclopentadienol generated by decomposition of ferrocenium cation;Tetrahedron Letters;2015-10
2. The stereochemical outcome of allyl magnesium and indium additions to 5-substituted norbornen-7-ones and its application to cis fused carbocycle formation via ring rearrangement metathesis;Organic & Biomolecular Chemistry;2012
3. Electrostatic origin towards the reversal of π-facial selectivity of 5,6-cis,exo-disubstituted bicyclic[2.2.2]oct-2-enes with m-chloroperbenzoic acid and diazomethane: a computational study;Tetrahedron Letters;2010-01
4. Orbital Phase Environments and Stereoselectivities;Orbitals in Chemistry;2009
5. Selective synthesis of multiply substituted 7-norbornenone derivatives or Diels–Alder cycloadducts from 1,2,3,4-tetrasubstituted 1,3-butadienes and maleic anhydride with or without Lewis acids;Tetrahedron;2008-10
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