B(C6F5)3 catalysed reduction of para-quinone methides and fuchsones to access unsymmetrical diaryl- and triarylmethanes: elaboration to beclobrate-Reference-Cited by-同舟云学术

B(C6F5)3 catalysed reduction of para-quinone methides and fuchsones to access unsymmetrical diaryl- and triarylmethanes: elaboration to beclobrate

Published:2017 Issue:39 Volume:15 Page:8393-8401
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Mahesh Sriram¹²³⁴,Vijaya Anand Ramasamy¹²³⁴^ORCID

Affiliation:

1. Department of Chemical Sciences

2. Indian Institute of Science Education and Research (IISER) Mohali

3. Manauli (PO)

4. India

Abstract

An effective method for the synthesis of diaryl- and triarylmethane derivatives through a Lewis acid catalyzed reduction of para-quinone methides and fuchsones, respectively, using the Hantzsch ester as a hydride surrogate is described.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB02007D

Reference125 articles.

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3. Taming Reactive Phenol Tautomers and o-Quinone Methides with Transition Metals: A Structure−Reactivity Relationship

4. ortho-Quinone Methides in Natural Product Synthesis

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