A novel ring closure and amine quaternization under eschweiler-clarke conditions

Author:

Smissman Edward E.,Weis James A.

Publisher

Wiley

Subject

Organic Chemistry

Reference6 articles.

1. M. Tomita, S. Uyeo, Jr., and T., Kikuchi, Tetrahedron Letters, 1053 (1964).

2. Oxazolidine formation in the attempted eschweiler-clarke reductive methylation ofcis-3-aminobicyclo[2.2.2] octan-2-ol

3. über Verbindungen mit Urotropin‐Struktur, VI. Mitteil.: Synthese des 1.3‐Diaza‐adamantans

4. Über Verbindungen mit Urotropin‐Struktur, IX. Zur Kenntnis des Bispidins

5. Melting points were obtained on a Thomas Hoover Unimelt and are corrected. Infrared data were recorded on a Beckman IR 10 spectrophotometer, and values are expressed in cm−1. Nmr data were recorded on a Varian Associates Model A-60 A spectrophotometer using 3-(trimethylsilyl)-1-propanesulfonic acid sodium salt as internal standard and deuterium oxide as solvent. All chemical shifts are in ppm (δ). Microanalyses were conducted by Midwest Microlab, Inc., Indianapolis, Ind.

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1. Split-UgiReaction with Chiral Compounds: Synthesis of Piperazine- and Bispidine-Based Peptidomimetics;Helvetica Chimica Acta;2016-04

2. Heteroadamantane;Advances in Heterocyclic Chemistry Volume 30;1982

3. Chemistry of 3-azabicyclo[3.3.1]nonanes;Chemical Reviews;1981-04-01

4. Use of the mannich reaction in the synthesis of bispidine;Journal of Heterocyclic Chemistry;1976-10

5. Analogues of sparteine. II. Synthesis of N-monoalkylbispidines and N,N'-dialkylbispidines;The Journal of Organic Chemistry;1976-04

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