Elaboration of 3,4-Dihydro-2H-pyran via  η2(3-Oxacyclohexyne)-Zirconocene

Michael C. J. Harris; Richard J. Whitby; Julian Blagg

doi:10.1055/s-1993-22580

Subscribe to RSS

Please copy the URL and add it into your RSS Feed Reader.

https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml

Share / Bookmark

Facebook X Linkedin Weibo

Download PDF

Synlett 1993; 1993(9): 705-707
DOI: 10.1055/s-1993-22580

letter

© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Elaboration of 3,4-Dihydro-2H-pyran via η²(3-Oxacyclohexyne)-Zirconocene

Michael C. J. Harris^* , Richard J. Whitby, Julian Blagg

^*Chemistry Department, The University, Southampton SO9 5NH, England

Further Information

Publication History

Publication Date:
19 March 2002 (online)

PDF Download Permissions and Reprints All articles of this category

β-hydrogen activation via loss of methane from 6-(zirconocene(methyl))-3,4-dihydro-2H-pyran affords η²-(3-oxacyclohexyne)-zirconocene which inserts unactivated alkenes and alkynes to afford elaborated dihydropyrans on aqueous work-up.

>