The multicomponent reaction of dimethoxycarbene, dimethyl butynedioate and electrophilic styrenes: an unprecedented synthesis of highly substituted cyclopentenone acetals

dc.contributor.author	Vijay Nair
dc.contributor.author	Beneesh, P B
dc.contributor.author	Sreekumar, V
dc.contributor.author	Bindu, S
dc.contributor.author	Rajeev S Menon
dc.contributor.author	Ani Deepthi
dc.date.accessioned	2021-02-08T11:57:59Z
dc.date.available	2021-02-08T11:57:59Z
dc.date.issued	2005
dc.identifier.citation	Tetrahedron Letters 46(2):201-203; 10 Jan 2005	en_US
dc.identifier.issn	0040-4039
dc.identifier.uri	http://hdl.handle.net/123456789/3661
dc.description.abstract	The zwitterionic species generated by the addition of dimethoxycarbene to dimethyl butynedioate is trapped by arylidenemalononitrile to yield cyclopentenone derivatives.	en_US
dc.language.iso	en	en_US
dc.publisher	Pergamon-Elsevier Science	en_US
dc.subject	Multicomponent reactions	en_US
dc.subject	Dimethoxycarbene	en_US
dc.subject	Zwitterions	en_US
dc.subject	Cyclopentenone	en_US
dc.title	The multicomponent reaction of dimethoxycarbene, dimethyl butynedioate and electrophilic styrenes: an unprecedented synthesis of highly substituted cyclopentenone acetals	en_US
dc.type	Article	en_US