Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
J Org Chem ; 80(14): 7266-74, 2015 Jul 17.
Article in English | MEDLINE | ID: mdl-26057617

ABSTRACT

Here, we report accessing small 3-fluoropyrrolidines and 3,3-difluoropyrrolidines through a 1,3-dipolar cycloaddition with a simple azomethine ylide and a variety of vinyl fluorides and vinyl difluorides. We demonstrate that vinyl fluorides within α,ß-unsaturated, styrenyl and even enol ether systems can participate in the cycloaddition reaction. The vinyl fluorides are relatively easy to synthesize through a variety of methods, making the 3-fluoropyrrolidines very accessible.


Subject(s)
Azo Compounds/chemistry , Pyrrolidines/chemical synthesis , Thiosemicarbazones/chemistry , Cycloaddition Reaction , Molecular Structure , Pyrrolidines/chemistry , Stereoisomerism
SELECTION OF CITATIONS
SEARCH DETAIL
...