Absolute configuration and conformation of 1,1′-spirobi [benz[f] indan]
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Conformational dependence of circular dichroism of 1,1′-spirobi[benz[e]indan]
2. Absolute configuration and conformation of 1,1′-spirob[benz[g]indan]
3. Optically active α- and β-naphthalene derivatives—IV
4. Circular dichroism of diastereomeric 3,3′-di-t-butyl-1,1′-spirobi-indans
5. Conformation dependence of circular dichroism of 1,1′-spirobi-indan
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1. Concise Synthesis of Arnottin I and (−)-Arnottin II;The Journal of Organic Chemistry;2006-12-01
2. One pot Synthesis of Fused Aromatics possessing Helical Chirality and Assignment of Absolute Configuration Assisted by Theoretical Circular Dichroism;Journal of Synthetic Organic Chemistry, Japan;2005
3. One-Pot Synthesis of Helical Aromatics: Stereoselectivity, Stability against Racemization, and Assignment of Absolute Configuration Assisted by Experimental and Theoretical Circular Dichroism;The Journal of Organic Chemistry;2004-10-20
4. Enantioselective dihydroxylation of olefins by osmium tetroxide in the presence of an optically active 1,1′-binaphthyl diamine derivative;Tetrahedron: Asymmetry;1996-10
5. Arnottin II, a unique spiro compound composed of a 3, 4-dehydro-1-tetralone and a phthalide skeleton: Is it biosynthetically related to a benzo[c]phenanthridine alkaloid ?;Tetrahedron Letters;1995-06
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