TY - JOUR
T1 - Recent Advances in Synthetic Methods for 2H-Pyrroles
AU - Choi, Seoung Mi
AU - Kim, Ju Hyun
N1 - Publisher Copyright:
© 2023 Wiley-VCH GmbH.
PY - 2024/1/9
Y1 - 2024/1/9
N2 - The compound, 2H-pyrrole, is a key scaffold contained in natural products, bioactive compounds, pharmaceuticals, and organic functional materials. However, the development of efficient synthetic strategies for 2H-pyrroles is challenging. This is because 2H-pyrroles, owing to their nonaromatic nature, are easily converted into the thermodynamically more stable 1H-pyrroles. Recently, efficient and straightforward synthetic strategies for 2H-pyrroles have been developed, including the dearomatization of 1H-pyrrole, oxidation of pyrrolines or pyrrolidines, ring construction via catalytic cycloaddition, and rearrangement of 3H-pyrroles. In this review, we summarize the progress in the research on 2H-pyrrole synthesis since 2000 and briefly discuss the synthesis reaction mechanisms.
AB - The compound, 2H-pyrrole, is a key scaffold contained in natural products, bioactive compounds, pharmaceuticals, and organic functional materials. However, the development of efficient synthetic strategies for 2H-pyrroles is challenging. This is because 2H-pyrroles, owing to their nonaromatic nature, are easily converted into the thermodynamically more stable 1H-pyrroles. Recently, efficient and straightforward synthetic strategies for 2H-pyrroles have been developed, including the dearomatization of 1H-pyrrole, oxidation of pyrrolines or pyrrolidines, ring construction via catalytic cycloaddition, and rearrangement of 3H-pyrroles. In this review, we summarize the progress in the research on 2H-pyrrole synthesis since 2000 and briefly discuss the synthesis reaction mechanisms.
KW - 2H-pyrrole
KW - Asymmetric catalysis
KW - Non-aromatic heterocycles
KW - Organocatalysis
KW - Transition metal catalysis
UR - http://www.scopus.com/inward/record.url?scp=85178964875&partnerID=8YFLogxK
U2 - 10.1002/adsc.202301238
DO - 10.1002/adsc.202301238
M3 - Review article
AN - SCOPUS:85178964875
SN - 1615-4150
VL - 366
SP - 2
EP - 17
JO - Advanced Synthesis and Catalysis
JF - Advanced Synthesis and Catalysis
IS - 1
ER -