Rh(I)-Catalyzed carbonylative [2+2+1] cycloaddition of bis(allene)s toward syntheses of natural products having (m-8-5) tricyclic ring systems

Please use this identifier to cite or link to this item: http://umt-ir.umt.edu.my:8080/handle/123456789/5121

Full metadata record

DC Field	Value	Language
dc.contributor.author	Soraya Shafawati Mohamad Tahier	-
dc.date.accessioned	2017-04-02T01:25:20Z	-
dc.date.available	2017-04-02T01:25:20Z	-
dc.date.issued	2013	-
dc.identifier.uri	http://hdl.handle.net/123456789/5121	-
dc.description.abstract	The cycloaddition reaction is one of the most attractive synthetic protocols for accessing a variety of scienfifically interesting and pharmaceutically useful ring skeletons and efficient method to generate cyclic compounds from simple starting materials	en_US
dc.language.iso	en	en_US
dc.publisher	Japan : Kanazawa University	en_US
dc.relation.ispartofseries	;QD 281 .R5 S6 2013	-
dc.subject	QD 281 .R5 S6 2013	en_US
dc.subject	Soraya Shafawati Mohamad Tahier	en_US
dc.subject	Tesis Kanazawa University 2013	en_US
dc.subject	Ring formation (Chemistry)	en_US
dc.title	Rh(I)-Catalyzed carbonylative [2+2+1] cycloaddition of bis(allene)s toward syntheses of natural products having (m-8-5) tricyclic ring systems	en_US
dc.type	Thesis	en_US
Appears in Collections:	Staff Thesis

Files in This Item:

File	Description	Size	Format
QD 281 .R5 S6 2013 FullText.pdf Restricted Access		5.06 MB	Adobe PDF	View/Open Request a copy

DSpace JSPUI