Regioselective Intermolecular [2 + 2]-Cycloaddition of α-Iodo-Unsaturated Ketones Promoted by Diisobutylaluminum Hydride.

Org Lett

Shannxi Key Laboratory of Phytochemistry, College of Chemistry and Chemical Engineering, Baoji University of Arts and Sciences, Baoji 721013, China.

Published: September 2016

The development of intermolecular [2 + 2]-cycloaddition of α-iodo-unsaturated ketones in the presence of diisobutylaluminum hydride (Dibal-H) is reported to produce various trispirocyclic derivatives containing a cyclobutane ring. This sequential lactonization/[2 + 2]-cycloaddition proceeds in high regioselectivity under mild conditions.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.orglett.6b02195DOI Listing

Publication Analysis

Top Keywords

intermolecular 2]-cycloaddition
8
2]-cycloaddition α-iodo-unsaturated
8
α-iodo-unsaturated ketones
8
diisobutylaluminum hydride
8
regioselective intermolecular
4
ketones promoted
4
promoted diisobutylaluminum
4
hydride development
4
development intermolecular
4
ketones presence
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!