2014
DOI: 10.1002/chin.201441156
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: Palladium‐Catalyzed Cycloaddition of Alkynyl Aryl Ethers to Allenes to Form a 2,3‐Bismethylidene‐2,3‐dihydro‐4H‐1‐benzopyran Framework.

Abstract: Palladium-Catalyzed Cycloaddition of Alkynyl Aryl Ethers to Allenes to Form a 2,3-Bismethylidene-2,3-dihydro-4H-1-benzopyran Framework. -The palladium-catalyzed cycloaddition of alkynyl aryl ethers (I) to various allenes gives benzopyran derivatives. The diene moieties of the cycloadducts are used as diene reaction partners in further Diels-Alder reactions to form linearly condensed tetracycles [cf. (VII)]. -(MINAMI, Y.; KANDA, M.; HIYAMA*, T.; Chem. Lett. 43 (2014) 2, 181-183, http://dx.doi.org/10.1246/cl.130… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Publication Types

Select...

Relationship

0
0

Authors

Journals

citations
Cited by 0 publications
references
References 1 publication
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?