Stereochemical studies of bicyclo[5.3.1]undecane-8,11-dione. Conformational analysis, enantiomer separation, CD-spectroscopy and enolization
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference48 articles.
1. Homoconjugation and transannular orbital interactions detected by photoelectron and carbon-13 NMR spectroscopy. Bicyclo[3.3.1]nona-3,7-diene-2,6-dione and bicyclo[3.3.1]nonane-2,6-dione
2. Synthesis of (R,R) and (S,S) bicyclo[3.3.0]octane-2,6-dione interactions between non-conjugated chromophores
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1. Synthesis and CD spectroscopic study of chiralC2-symmetric (+)-2-oxaadamantane-4,8-dione;Chirality;2005
2. Chiral bicyclic keto lactones: determination of the absolute configuration by the study of chiroptical properties and chemical correlation;Tetrahedron: Asymmetry;2004-08
3. Synthesis, chiroptical properties and absolute configuration of spiro[1,3-benzodioxole-methanocyclooct[b]indole];Organic & Biomolecular Chemistry;2002-12-09
4. Enantiomer separation and absolute configuration of densely functionalized 2-oxatricyclo[4.3.1.03,8]decanes by CD spectroscopy and chemical correlation;Tetrahedron: Asymmetry;2000-08
5. Intramolecular ring closure via ether bond in reaction of α,α′-halogeno bicyclo[3.3.1]nonanediones under basic conditions;Journal of the Chemical Society, Perkin Transactions 1;1999
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