Journal
RUSSIAN CHEMICAL BULLETIN
Volume 54, Issue 10, Pages 2432-2436Publisher
SPRINGER
DOI: 10.1007/s11172-006-0133-2
Keywords
1,3-dipolar cycloaddition; 3-arylideneindolin-2-ones; azomethine ylides; spiro[indoline-3,3 '-pyrrolidine]; regioselectivity; X-ray diffraction study
Categories
Ask authors/readers for more resources
A series of 6a',7',8',9'-tetrahydrospiro[indoline-3,7'-pyrrolo[1,2-a]quinoline]-2-one derivatives were synthesized by the 1,3-dipolar cycloaddition reaction. The regio- and stereoselectivity of the reaction were established by X-ray diffraction study.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available
Share Paper
