PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
May 7, 2026Advanced Synthesis & Catalysis1 citations

NaIO 4 ‐Promoted Selenylation/Cyclization Reactions of 1‐(2‐(Vinyloxy)aryl)‐Indoles to Assemble Selenized Benzo5,61,4oxazino4,3‐ a indole Derivatives

View Full Paper
YRYuchen RongJiangsu Normal UniversityJYJing YangJiangsu Normal UniversityXCXingyue ChenJiangsu Normal University

Key Points

  • This research aims to synthesize selenized benzo[5,6][1,4]oxazino[4,3‐ a ]indole derivatives using NaIO 4.
  • Utilized NaIO 4 to promote the selenylation/cyclization of 1‐(2‐(vinyloxy)aryl)‐indoles with diselenides.
  • Explored wide substrate scope and high group tolerance in reactions.
  • Successfully synthesized selenized benzo[5,6][1,4]oxazino[4,3‐ a ]indole derivatives.
  • Achieved good yields in the reactions.

Abstract

The NaIO 4 ‐promoted selenylation/cyclization of 1‐(2‐(vinyloxy)aryl)‐indoles with diselenides has been reported for the synthesis of selenized benzo5,61,4oxazino4,3‐ a indole derivatives. In this synthesis, the indole moiety with significant medicinal value, the morpholine skeleton, and the selenium group were introduced into a privileged structure, resulting in the target compound with potential value. The reaction features wide substrate scope, high group tolerance and good yield, which also represents the first selenylation/cyclization of 1‐(2‐(vinyloxy)aryl)‐indoles and diselenides.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Rong et al. (2026) studied this question.

synapsesocial.com/papers/69fbef68164b5133a91a3352https://doi.org/10.1002/adsc.70489
Ask AI
Helpful
Bookmark
Share
View Full Paper