Recent Developments for the Ring Opening of Pyrrolidines and Unstrained Cyclic Amines via C–N Bond Cleavage
Publication type: Journal Article
Publication date: 2025-04-10
scimago Q2
wos Q2
SJR: 0.558
CiteScore: 4.3
Impact factor: 2.7
ISSN: 1434193X, 10990690
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.
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Ota E., Yamaguchi J. Recent Developments for the Ring Opening of Pyrrolidines and Unstrained Cyclic Amines via C–N Bond Cleavage // European Journal of Organic Chemistry. 2025. Vol. 28. No. 20. e202401322
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Ota E., Yamaguchi J. Recent Developments for the Ring Opening of Pyrrolidines and Unstrained Cyclic Amines via C–N Bond Cleavage // European Journal of Organic Chemistry. 2025. Vol. 28. No. 20. e202401322
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TY - JOUR
DO - 10.1002/ejoc.202401322
UR - https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.202401322
TI - Recent Developments for the Ring Opening of Pyrrolidines and Unstrained Cyclic Amines via C–N Bond Cleavage
T2 - European Journal of Organic Chemistry
AU - Ota, Eisuke
AU - Yamaguchi, Junichiro
PY - 2025
DA - 2025/04/10
PB - Wiley
IS - 20
VL - 28
SN - 1434-193X
SN - 1099-0690
ER -
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@article{2025_Ota,
author = {Eisuke Ota and Junichiro Yamaguchi},
title = {Recent Developments for the Ring Opening of Pyrrolidines and Unstrained Cyclic Amines via C–N Bond Cleavage},
journal = {European Journal of Organic Chemistry},
year = {2025},
volume = {28},
publisher = {Wiley},
month = {apr},
url = {https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.202401322},
number = {20},
pages = {e202401322},
doi = {10.1002/ejoc.202401322}
}