High exo-endo rate ratio and predominate exo substitution in the solvolysis of 2-p-anisylnorbornyl derivatives. The characteristics of a highly stabilized, classical norbornyl cation (Englisch)
Nationallizenz
- Neue Suche nach: Brown, Herbert C.
- Neue Suche nach: Takeuchi, Kenichi.
- Neue Suche nach: Brown, Herbert C.
- Neue Suche nach: Takeuchi, Kenichi.
In:
Journal of the American Chemical Society
;
90
, 10
;
2691-2693
;
1968
-
ISSN:
- Aufsatz (Zeitschrift) / Elektronische Ressource
-
Titel:High exo-endo rate ratio and predominate exo substitution in the solvolysis of 2-p-anisylnorbornyl derivatives. The characteristics of a highly stabilized, classical norbornyl cation
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Weitere Titelangaben:J. Am. Chem. Soc.
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Beteiligte:Brown, Herbert C. ( Autor:in ) / Takeuchi, Kenichi. ( Autor:in )
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Erschienen in:Journal of the American Chemical Society ; 90, 10 ; 2691-2693
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Verlag:
- Neue Suche nach: American Chemical Society
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Erscheinungsdatum:01.05.1968
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ISSN:
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Coden:
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DOI:
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Medientyp:Aufsatz (Zeitschrift)
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Format:Elektronische Ressource
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Sprache:Englisch
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Datenquelle:
Inhaltsverzeichnis – Band 90, Ausgabe 10
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- 2583
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- 2587
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- 2606
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- 2612
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- 2622
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- 2638
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- 2646
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- 2651
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- 2656
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- 2661
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- 2669
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- 2677
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- 2681
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- 2691
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High exo-endo rate ratio and predominate exo substitution in the solvolysis of 2-p-anisylnorbornyl derivatives. The characteristics of a highly stabilized, classical norbornyl cationBrown, Herbert C. / Takeuchi, Kenichi. et al. | 1968
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- 2694
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- 2696
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- 2699
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- 2700
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- 2702
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- 2704
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- 2706
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- 2707
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- 2709
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- 2710
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- 2711
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- 2713
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- 2714
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- 2715
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- 2721
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- 2724
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- 2726
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- 2730
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