Diastereoselective synthesis of functionalised carbazoles via a sequential Diels–Alder/ene reaction strategy-Reference-Cited by-同舟云学术

Diastereoselective synthesis of functionalised carbazoles via a sequential Diels–Alder/ene reaction strategy

Published:2015 Issue:21 Volume:5 Page:16125-16152
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Cowell Joseph¹²³⁴,Abualnaja Matokah¹²³⁴,Morton Stephanie¹²³⁴,Linder Ruth¹²³⁴,Buckingham Faye¹²³⁴,Waddell Paul G.¹²³⁴,Probert Michael R.¹²³⁴,Hall Michael J.¹²³⁴

Affiliation:

1. School of Chemistry

2. Newcastle University

3. Newcastle upon Tyne

4. UK

Abstract

A one-pot, three-component, synthesis of saturated carbazoles and related pyridazino[3,4-b]indoles is described, involving an intermolecular Diels–Alder/intermolecular ene reaction sequence with relative stereocontrol of up to four stereocentres.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA00499C

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