The synthesis of substituted amino[2.2]paracyclophanes-Reference-Cited by-同舟云学术

The synthesis of substituted amino[2.2]paracyclophanes

Published:2016 Issue:46 Volume:14 Page:10848-10860
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Jayasundera Krishanthi P.¹²³⁴,Kusmus Disraëli N. M.¹²³⁴⁵,Deuilhé Lise¹²³⁴⁶,Etheridge Leonie¹²³⁴,Farrow Zane¹²³⁴,Lun David J.¹²³⁴,Kaur Gurpreet¹²³⁴,Rowlands Gareth J.¹²³⁴^ORCID

Affiliation:

1. Institute of Fundamental Sciences

2. Massey University

3. Palmerston North

4. New Zealand

5. Vrije Universiteit Amsterdam

6. Ecole Nationale Supérieure de Chimie de Rennes

Abstract

Amino[2.2]paracyclophanes can be prepared by direct amination of bromo[2.2]paracyclophanes or more generally by a formylation–oxime formation–oxidation–Lossen-like rearrangement sequence.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB02150F

Reference114 articles.

1. Syntheses and applications of disubstituted [2.2]paracyclophanes

2. [2.2]Paracyclophane Derivatives: Synthesis and Application in Catalysis

3. Modern Cyclophane Chemistry, ed. R. Gleiter and H. Hopf, Wiley-VCH, Weinheim, 2004

4. The synthesis of enantiomerically pure [2.2]paracyclophane derivatives

5. [2.2]Paracyclophane derivatives in asymmetric catalysis

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