Synthesis, C–H bond functionalisation and cycloadditions of 6-styryl-1,2-oxathiine 2,2-dioxides-Reference-Cited by-同舟云学术

Synthesis, C–H bond functionalisation and cycloadditions of 6-styryl-1,2-oxathiine 2,2-dioxides

Published:2021 Issue:29 Volume:19 Page:6431-6446
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Gabbutt Christopher D.¹²³⁴⁵^ORCID,Heron B. Mark¹²³⁴⁵^ORCID,Lilly Thomas¹²³⁴⁵,Ogwang Ochola W.¹²³⁴⁵,Zonidis Dimitrios¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemical Sciences

2. School of Applied Sciences

3. University of Huddersfield

4. Huddersfield

5. UK

Abstract

1,2-Oxathiine 2,2-dioxides readily undergo C–H activated coupling at C-3. The 6-styryl derivatives participate in cycloadditions with PTAD to afford 1H-[1,2]oxathiino[5,6-c][1,2,4]triazolo[1,2-a]pyridazine-1,3(2H)-dione 8,8-dioxides.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB01125A

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