Recent Developments for the Ring Opening of Pyrrolidines and Unstrained Cyclic Amines via C−N Bond Cleavage | Zendy

Ota Eisuke | Zendy; Yamaguchi Junichiro | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Recent Developments for the Ring Opening of Pyrrolidines and Unstrained Cyclic Amines via C−N Bond Cleavage

Author(s) -

Ota Eisuke,

Yamaguchi Junichiro

Publication year - 2025

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.202401322

Subject(s) - chemistry , cyclic amines , cleavage (geology) , bond cleavage , ring (chemistry) , stereochemistry , combinatorial chemistry , organic chemistry , amine gas treating , catalysis , geotechnical engineering , fracture (geology) , engineering

Abstract In recent years, the deconstructive transformation of unstrained cyclic amines via C−N bond cleavage has emerged as a powerful strategy for expanding chemical space and facilitating the synthesis of structurally diverse molecules. Notably, advancements in the C−N bond cleavage of pyrrolidine and other unstrained cyclic amines have highlighted the significant potential of this approach in modern organic synthesis. This concept reviews recent developments in the C−N bond cleavage reaction, with a primary focus on pyrrolidines, while also exploring broader progress in related systems.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research