Absolute configuration and conformation of 1,1′-spirob[benz[g]indan]
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
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4. Conformation dependence of circular dichroism of 1,1′-spirobi-indan
5. 723. The proton resonance spectra and conformations of the prolines. Part III. Hydroxyproline and allohydroxyproline in acid and alkaline solution
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1. Compounds with Chiral Axes, Planes, etc. Gyrochiral Compounds;Atlas of Stereochemistry;1986
2. Liquid chromatographic optical resolution of 2,2′-spirobibenz[e]indan derivatives and absolute stereochemistry as determined by the c.d. exciton chirality method;J. Chem. Soc., Perkin Trans. 1;1985
3. ChemInform Abstract: ABSOLUTE CONFIGURATION AND CONFORMATION OF 1,1′-SPIROBI(BENZ(G)INDAN);Chemischer Informationsdienst;1981-03-03
4. Absolute configuration and conformation of 1,1′-spirobi [benz[f] indan];Tetrahedron Letters;1981-01
5. Optisch aktive, aromatische Spirane, 11. Mitt.: Synthese optisch aktiver mono- bis heptasubstituierter 5-Methyl- und 5-Ethyl-2,2?-spirobiindane und analoger Naphthalinderivate bekannter Chiralit�t und enantiomerer Reinheit;Monatshefte f�r Chemie;1981
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