Palladium-catalyzed highly regioselective mono and double Sonogashira cross-coupling reactions of 5-substituted-1,2,3-triiodobenzene under ambient conditions-Reference-Cited by-同舟云学术

Palladium-catalyzed highly regioselective mono and double Sonogashira cross-coupling reactions of 5-substituted-1,2,3-triiodobenzene under ambient conditions

Published:2020 Issue:28 Volume:10 Page:16366-16376
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Al-Zoubi Raed M.¹²³⁴^ORCID,Al-Omari Mothana K.¹²³⁴^ORCID,Al-Jammal Walid K.¹²³⁴^ORCID,Ferguson Michael J.¹⁵⁶⁷⁸^ORCID

Affiliation:

1. Department of Chemistry

2. Jordan University of Science and Technology

3. Irbid

4. Jordan

5. Gunning-Lemieux Chemistry Centre

6. University of Alberta

7. Edmonton

8. Canada

Abstract

Efficient and highly regioselective synthesis of 2,3-diiodinated diphenylacetylene and iodinated meta-terphenylacetylene derivatives via mono and double Sonogashira cross-coupling reactions.

Funder

Jordan University of Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/RA/D0RA01569E

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1. Halogenated diarylacetylenes repress c-myc expression in cancer cells

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3. Toward Antikekulene: Angular 1,2-Di-, 2,3-Di-, and 1,2,15,16-Tetrachloro[6]phenylene