Intramolecular thermal stepwise [2 + 2] cycloadditions: investigation of a stereoselective synthesis of [n.2.0]-bicyclolactones-Reference-Cited by-同舟云学术

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Intramolecular thermal stepwise [2 + 2] cycloadditions: investigation of a stereoselective synthesis of [n.2.0]-bicyclolactones

Published:2016 Issue:40 Volume:14 Page:9554-9559
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Throup Adam¹²³⁴,Patterson Laurence H.¹²³⁴,Sheldrake Helen M.¹²³⁴^ORCID

Affiliation:

1. Institute of Cancer Therapeutics

2. University of Bradford

3. Bradford

4. UK

Abstract

A new method for the synthesis of highly functionalised cyclobutenes.

Funder

Yorkshire Cancer Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB01661H

Reference29 articles.

1. Enantiomerically Pure Cyclobutane Derivatives and Their Use in Organic Synthesis

2. Stereoselective Preparation of Cyclobutanes with Four Different Substituents: Total Synthesis and Structural Revision of Pipercyclobutanamide A and Piperchabamide G

3. Cyclobutane and Cyclobutene Synthesis: Catalytic Enantioselective [2+2] Cycloadditions

4. Bioactive cyclobutane-containing alkaloids

5. Cyclobutane-Containing Alkaloids: Origin, Synthesis, and Biological Activities

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