indium-mediated allylation of a-tert-butylsulfinylaldimines with dimethyl 2-[2-(chloromethyl)allyl]malonate
Joint Authors
Dima, Haytham K.
Foubelo, Francisco
Yus, Miguel
Source
Issue
Vol. 6, Issue 3 (30 Sep. 2011), pp.247-255, 9 p.
Publisher
Yarmouk University Deanship of Research and Graduate Studies
Publication Date
2011-09-30
Country of Publication
Jordan
No. of Pages
9
Main Subjects
Abstract EN
The reaction of N-fert-butylsulfinylaldimines 5 with dimethyl 2-[2-(chloromethyl) allyl]-malonate (10), in the presence of indium metal and sodium iodide, at room temperature for 72 hours, led to the corresponding amino ester derivative 11.
The reaction proceeded in high yields and in a total stereoselective fashion, a single diastereoisomer being always isolated.
American Psychological Association (APA)
Dima, Haytham K.& Foubelo, Francisco& Yus, Miguel. 2011. indium-mediated allylation of a-tert-butylsulfinylaldimines with dimethyl 2-[2-(chloromethyl)allyl]malonate. Jordan Journal of Chemistry،Vol. 6, no. 3, pp.247-255.
https://search.emarefa.net/detail/BIM-270257
Modern Language Association (MLA)
Dima, Haytham K.…[et al.]. indium-mediated allylation of a-tert-butylsulfinylaldimines with dimethyl 2-[2-(chloromethyl)allyl]malonate. Jordan Journal of Chemistry Vol. 6, no. 3 (Sep. 2011), pp.247-255.
https://search.emarefa.net/detail/BIM-270257
American Medical Association (AMA)
Dima, Haytham K.& Foubelo, Francisco& Yus, Miguel. indium-mediated allylation of a-tert-butylsulfinylaldimines with dimethyl 2-[2-(chloromethyl)allyl]malonate. Jordan Journal of Chemistry. 2011. Vol. 6, no. 3, pp.247-255.
https://search.emarefa.net/detail/BIM-270257
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 254-255
Record ID
BIM-270257
