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Access to 6-hydroxy indolizines and related imidazo[1,5-a]pyridines through the SN2 substitution/condensation/tautomerization cascade process.


ABSTRACT: A simple and efficient cascade reaction was developed for the construction of hydroxy substituted indolizines from pyrrole-2-carbaldehydes and commercially available 4-halogenated acetoacetic esters. Their optical properties were also evaluated.

SUBMITTER: Duan G 

PROVIDER: S-EPMC9036982 | biostudies-literature | 2021 Jul

REPOSITORIES: biostudies-literature

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Access to 6-hydroxy indolizines and related imidazo[1,5-<i>a</i>]pyridines through the S<sub>N</sub>2 substitution/condensation/tautomerization cascade process.

Duan Guiyun G   Liu Hao H   Zhang Liqing L   Yuan Chunhao C   Li Yongchao Y   Ge Yanqing Y  

RSC advances 20210723 41


A simple and efficient cascade reaction was developed for the construction of hydroxy substituted indolizines from pyrrole-2-carbaldehydes and commercially available 4-halogenated acetoacetic esters. Their optical properties were also evaluated. ...[more]

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