Monometallation of a di(aminoaryl) ether induces a Smiles rearrangement leading to a sodium aryloxide complex: the synthesis and crystal structure of [(MeOCH2CH2)(C6H4NHCH2CH2OMe)NC6H4O·Na]2-Reference-Cited by-同舟云学术

Monometallation of a di(aminoaryl) ether induces a Smiles rearrangement leading to a sodium aryloxide complex: the synthesis and crystal structure of [(MeOCH2CH2)(C6H4NHCH2CH2OMe)NC6H4O·Na]2

Published:1993 Issue:17 Volume: Page:1355-1357
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Cragg-Hine Ian,Davidson Matthew G.,Kocian Oldrich,Kottke Thomas,Mair Francis S.,Snaith Ronald,Stoddart J. Fraser

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1993/C3/C39930001355

Reference20 articles.

1. M. Fieser , Reagents for Organic Synthesis, vol. 15, Interscience, New York, 1990, Vol. 15 and earlier volumes give specific uses of alkali metal reagents.

2. Structures of Organonitrogen—Lithium Compounds: Recent Patterns and Perspectives in Organolithium Chemistry

3. Meldola Medal Lecture. Ring-stacking and ring-laddering in organonitrogenlithium compounds: the development of concepts with wide applicability throughout lithium structural chemistry

4. Struktur und Reaktivität von Lithiumenolaten, vom Pinakolon zur selektivenC-Alkylierung von Peptiden – Schwierigkeiten und Möglichkeiten durch komplexe Strukturen

5. Structure and Reactivity of Lithium Enolates. From Pinacolone to SelectiveC-Alkylations of Peptides. Difficulties and Opportunities Afforded by Complex Structures

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