Face Selectivity in the Borohydride Reduction of 4-eq,6-ax-Diaryl-5-azaadamantan-2-ones
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Reference13 articles.
1. Geometric equivalents of enantiomers in studies of the stereochemical course of substitution at carbon. Electronic effects in nucleophilic addition to carbonyl groups and to carbocations. Virtual proof of the existence of .sigma. participation by unstrained carbon-carbon bonds
2. Transmission of polar substituent effects in the adamantane ring system as monitored by 19F NMR: hyperconjugation as a stereoinductive factor
3. Electrostatic vs Hyperconjugative Effects as Stereoinductive Factors in the Adamantane Ring System
4. Strongly enhanced stereoselectivity in the reduction of 5-substituted adamantanones by substitution of C5 by positive nitrogen
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1. Microwave-assisted aza-Prins reaction. Part 2: straightforward access to 2,6-disubstituted 1-azaadamantanes;Tetrahedron Letters;2011-12
2. Assessable Consequences of Through-Bond Donor–Acceptor Interactions in β-Aminoketones;Chemistry - A European Journal;2008-02-08
3. Experimental and theoretical structural study of 2,9-bis-(4-fluorophenyl)-azaadamantan-4-one ethylene ketal;Journal of Molecular Structure;2003-07
4. 1H and 13C NMR investigation of 2-eq,9-ax-diaryl-azaadamantan-4-ones;Journal of Molecular Structure;2002-02
5. 2,9-Bis(3-nitrophenyl)-1-azaadamantan-4-one;Acta Crystallographica Section C Crystal Structure Communications;2001-07-09
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