PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 9, 2024Advanced Synthesis & Catalysis10 citations

Visible Light‐Induced Copper‐Catalyzed Alkylation/exo‐Cyclization of 1,7‐Dienes with Sulfonium Salts to Access Sulfur‐Containing Polycyclic Compounds

View Full Paper
XLXin‐Qian LiuJFJian‐Hong FanKTKewen Tang

Key Points

Key points are not available for this paper at this time.

Abstract

Abstract A direct visible‐light‐promoted radical‐triggered tandem cyclization of 1,7‐diene systems with cyclic sulfonium salts by using copper(I)‐based complexes as photoredox catalyst is developed. With this approach, a variety of sulfur‐containing polycyclic derivatives are prepared through alkylation/ 6‐exo‐trig cyclization/ 5‐exo‐trig cyclization of 1,7‐diene systems under mild conditions. In addition, the photoinduced copper‐catalyzed ring‐opening of cyclic sulfonium salts provides the alkyl radical intermediates, which prefers addition to the C−C double bond that connected to the aromatic ring rather than the electron‐deficient vinyl in 1,7‐dienes. Moreover, oxidation of the desired sulfur‐containing polycyclic products provides a strategy for the preparation of remote nitrogen‐fused polycyclic substituted sulfoxide or sulfone‐containing derivatives.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Liu et al. (2024) studied this question.

synapsesocial.com/papers/68e60e4db6db6435875a14b5https://doi.org/10.1002/adsc.202400445
Ask AI
Helpful
Bookmark
Share
View Full Paper