AgI‐promoted one‐pot synthesis of aminoindolizines via sequential Mannich‐Grignard addition and intramolecular cyclization in water

The efficient synthesis of aminoindolizines in ecofriendly water with broad substrate scope from the mild and readily available AgI‐catalyzed one‐pot three‐component reaction of pyridine‐2‐carboxaldehyde, secondary amines, and terminal alkynes proceeds through the sequential Mannich‐Grignard additio...

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Published in:Journal of heterocyclic chemistry Vol. 58; no. 3; pp. 900 - 904
Main Authors: Guguloth, Veeranna, Balaboina, Ramesh, Paidakula, Suresh, Thirukovela, Narasimha S., Vadde, Ravinder
Format: Journal Article
Language:English
Published: Chichester, UK John Wiley & Sons, Inc 01-03-2021
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Abstract The efficient synthesis of aminoindolizines in ecofriendly water with broad substrate scope from the mild and readily available AgI‐catalyzed one‐pot three‐component reaction of pyridine‐2‐carboxaldehyde, secondary amines, and terminal alkynes proceeds through the sequential Mannich‐Grignard addition as well as intramolecular cyclization was reported for the first time.
AbstractList The efficient synthesis of aminoindolizines in ecofriendly water with broad substrate scope from the mild and readily available AgI‐catalyzed one‐pot three‐component reaction of pyridine‐2‐carboxaldehyde, secondary amines, and terminal alkynes proceeds through the sequential Mannich‐Grignard addition as well as intramolecular cyclization was reported for the first time.
Author Thirukovela, Narasimha S.
Balaboina, Ramesh
Paidakula, Suresh
Guguloth, Veeranna
Vadde, Ravinder
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  doi: 10.1111/j.1528-1157.1978.tb04507.x
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Snippet The efficient synthesis of aminoindolizines in ecofriendly water with broad substrate scope from the mild and readily available AgI‐catalyzed one‐pot...
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wiley
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StartPage 900
SubjectTerms Alkynes
Amines
Substrates
Synthesis
Title AgI‐promoted one‐pot synthesis of aminoindolizines via sequential Mannich‐Grignard addition and intramolecular cyclization in water
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjhet.4184
https://www.proquest.com/docview/2494683673
Volume 58
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