Substituent effects of alkoxy and amino groups directly bonded to cationic carbon in the perpendicularly twisted geometry. 2-Oxa- and 2-aza-1-adamantyl tosylates

William P. Meyer; J. C. Martin

doi:10.1021/ja00421a030

journal article Mar 01, 1976

Substituent effects of alkoxy and amino groups directly bonded to cationic carbon in the perpendicularly twisted geometry. 2-Oxa- and 2-aza-1-adamantyl tosylates

William P. Meyer J. C. Martin

Journal of the American Chemical Society Vol. 98 No. 5 pp. 1231-1241 · American Chemical Society (ACS)

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Easy synthesis of 7-alkylbicyclo[3.3.1]non-6-en-3-ones by silica gel-promoted fragmentation of 3-alkyl-2-oxaadamant-1-yl mesylates

Pelayo Camps, Rachid El Achab · 1996

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Details

Published: Mar 01, 1976
Vol/Issue: 98(5)
Pages: 1231-1241

Authors

Inserm U1062, Inra U1260, Faculté de Médecine 13385 Marseille France; Aix Marseille Université Marseille France

Cite This Article

William P. Meyer, J. C. Martin (1976). Substituent effects of alkoxy and amino groups directly bonded to cationic carbon in the perpendicularly twisted geometry. 2-Oxa- and 2-aza-1-adamantyl tosylates. Journal of the American Chemical Society, 98(5), 1231-1241. https://doi.org/10.1021/ja00421a030

Substituent effects of alkoxy and amino groups directly bonded to cationic carbon in the perpendicularly twisted geometry. 2-Oxa- and 2-aza-1-adamantyl tosylates

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