Chemoselectivity and stereoselectivity of cyclisation pathways leading to bicyclic tetramates controlled by ring-chain tautomerisation in thiazolidines-Reference-Cited by-同舟云学术

Chemoselectivity and stereoselectivity of cyclisation pathways leading to bicyclic tetramates controlled by ring-chain tautomerisation in thiazolidines

Published:2016 Issue:19 Volume:14 Page:4464-4478
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Panduwawala Tharindi D.¹²³⁴⁵,Iqbal Sarosh¹²³⁴⁵,Tirfoin Rémi¹²³⁴⁵,Moloney Mark G.¹²³⁴⁵

Affiliation:

1. Department of Chemistry

2. Chemistry Research Laboratory

3. The University of Oxford

4. Oxford

5. UK

Abstract

N-Malonyl thiazolidine templates derived from cysteine and aromatic aldehydes may be used to access bicyclic tetramates.

Funder

Medical Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB00557H

Reference26 articles.

1. Tetramic and tetronic acids: An update on new derivatives and biological aspects

2. Naturally Occurring Tetramic Acids: Structure, Isolation, and Synthesis

3. Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives

4. Novel chiral pyrrolidinone scaffolds derived from threonine with antibacterial activity

5. Stereoselectivity in the Reduction of Bicyclic Tetramates

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