2004
DOI: 10.1002/chin.200443063
|View full text |Cite
|
Sign up to set email alerts
|

Facile and Selective Deallylation of Allyl Ethers Using Diphosphinidenecyclobutene‐Coordinated Palladium Catalysts.

Abstract: Deprotection O 0345 Facile and Selective Deallylation of Allyl Ethers Using Diphosphinidenecyclobutene-Coordinated Palladium Catalysts. -PPC is found to be an efficient catalyst for the deallylation of various allyl ethers in aniline. A number of functional groups are tolerated under these conditions. Selective deallylation of the allyl ether group in the presence of allyl ester moiety is possible. Allylic carbamates [cf. (VIII)] undergo cleavage into amines and CO 2 . -(MURAKAMI, H.; MINAMI, T.; OZAWA*, F.; J… 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 9 publications
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?