Green and rapid acid-catalyzed ynamide skeletal rearrangement and stereospecific functionalization with anisole derivatives-Reference-Cited by-同舟云学术

Green and rapid acid-catalyzed ynamide skeletal rearrangement and stereospecific functionalization with anisole derivatives

Published:2023 Issue:20 Volume:25 Page:8124-8133
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Mutra Mohana Reddy¹^ORCID,Chandana T. L.¹,Wang Yun-Jou¹,Wang Jeh-Jeng¹²^ORCID

Affiliation:

1. Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, No. 100, Shiquan 1st Rd, Sanmin District, Kaohsiung City, 807, Taiwan

2. Department of Medical Research, Kaohsiung Medical University Hospital, No. 100 Tzyou 1st Rd, Sanmin District, Kaohsiung City 807, Taiwan

Abstract

Environmentally friendly acid-catalyzed 2-alkynyl-ynamides (N–Csp) bond cleavage, alkyne migration and stereospecific functionalization with anisole derivatives for the synthesis of challenging indole scaffolds in 5–10 minutes.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/GC/D3GC02460A

Reference51 articles.

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3. Umpolung Reactivity of Ynamides: An Unconventional [1,3]‐Sulfonyl and [1,5]‐Sulfinyl Migration Cascade

4. Ynamides as Three-Atom Components in Cycloadditions: An Unexplored Chemical Reaction Space

5. Gold-Catalyzed Atom-Economic Synthesis of Sulfone-Containing Pyrrolo[2,1-a]isoquinolines from Diynamides: Evidence for Consecutive Sulfonyl Migration

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