2015
DOI: 10.1002/chin.201547187
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: Stereoselective Bromocyclization of Allylated Aldoxime Ethers

Abstract: Stereoselective Bromocyclization of Allylated Aldoxime Ethers -Bromination of O-allylated aldoxime ethers having a trans substituted allyl group with Br(collidine) 2PF6 induces an efficient diastereoselective cyclization to give 5-bromooxazine derivatives. The cis-substituted allyl substrate (VII) produces a mixture from which the isoxazoline (VIII) can be isolated. -(EGART, B.; CZEKELIUS*, C.; Chem. -Asian J. 9 (2014) 8, Special Issue, 2088-2091, http://dx.

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?