Facile Diastereoselective Synthesis of Highly Substituted Alkylene‐oxetanes from 3‐Alkyl Allenoates and Diaryl 1,2‐Diones/α‐Ketoamides Mediated by DBU

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DC Field	Value	Language
dc.contributor.author	Krishnan, J	-
dc.contributor.author	Mayadevi, T S	-
dc.contributor.author	Varughese, S	-
dc.contributor.author	Vijay Nair	-
dc.date.accessioned	2019-06-26T15:01:11Z	-
dc.date.available	2019-06-26T15:01:11Z	-
dc.date.issued	2019-02-21	-
dc.identifier.citation	European Journal of Organic Chemistry; 7:1557-1561	en_US
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1002/ejoc.201801747	-
dc.identifier.uri	http://10.10.100.66:8080/xmlui/handle/123456789/3372	-
dc.description.abstract	A facile tertiary amine‐mediated [2+2] annulation reaction of 3‐alkyl allenoates, and diaryl 1,2‐diones leading to diastereoselective synthesis of highly substituted alkylene‐oxetane derivatives is reported. The reaction was further extended to α‐ketoamides. The obtained amide‐appended oxetanes were transformed to 5‐methylene‐1H‐pyrrol‐2(5H)‐one derivatives with potential biological activity.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Zwitterions	en_US
dc.subject	Allenes	en_US
dc.subject	Cycloaddition	en_US
dc.subject	Oxygen heterocycles	en_US
dc.title	Facile Diastereoselective Synthesis of Highly Substituted Alkylene‐oxetanes from 3‐Alkyl Allenoates and Diaryl 1,2‐Diones/α‐Ketoamides Mediated by DBU	en_US
dc.type	Article	en_US
Appears in Collections:	2019

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