TEMPO promoted direct multi-functionalization of terminal alkynes with 2-oxindoles/benzofuran-2(3H)-one-Reference-Cited by-同舟云学术

TEMPO promoted direct multi-functionalization of terminal alkynes with 2-oxindoles/benzofuran-2(3H)-one

Published:2018 Issue:29 Volume:16 Page:5228-5231
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Liu Qi¹²³⁴⁵,Liu Jie-Jie¹²³⁴⁵,Cheng Liang¹²³⁴⁵^ORCID,Wang Dong¹²³⁴⁵,Liu Li¹²³⁴⁵

Affiliation:

1. Beijing National Laboratory for Molecular Sciences (BNLMS)

2. CAS Key Laboratory of Molecular Recognition and Function

3. CAS Research/Education Center for Excellence in Molecular Sciences

4. Institute of Chemistry

5. Chinese Academy of Sciences

Abstract

Highly selective and catalyst-free tandem multi-functionalization of terminal alkynes was developed with 2-oxindoles and benzo-furan-2(3H)-one using TEMPO both as a radical promoter and a trapping reagent.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Beijing Municipality

China Association for Science and Technology

Chinese Academy of Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB01380B

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