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Synthesis of Cyclopropanes via Organoiron Methodology: Preparation of rac -Dysibetaine CPa

โœ Scribed by Siddiquee, Tasneem A.; Lukesh, Julie M.; Lindeman, Sergey; Donaldson, William A.


Book ID
126005411
Publisher
American Chemical Society
Year
2007
Tongue
English
Weight
76 KB
Volume
72
Category
Article
ISSN
0022-3263

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Synthesis of Cyclopropanes via Organoiro
โœ Rajesh K. Pandey; Sergey Lindeman; William A. Donaldson ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons โš– 27 KB ๐Ÿ‘ 2 views

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Synthesis of cyclopropanes via organoiro
โœ Kamil Godula; William A Donaldson ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 55 KB

A route to 1,2,3-trisubstituted cyclopropanes has been developed. The relative stereochemistry at the three cyclopropane centers is established by nucleophilic attack on the pentadienyl ligand on the face opposite to iron and subsequent oxidatively induced reductive elimination with retention of con

Synthesis of cyclopropanes via organoiro
โœ Nathaniel J Wallock; William A Donaldson ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 80 KB

A stereoselective route to cis-2-(2%-carboxycyclopropyl)glycine has been developed. exo-Nucleophilic addition to the (bicyclo[5.1.0]octadienyl)iron(1+) cation establishes the relative stereochemistry at the cyclopropane ring and the a-stereocenter. Subsequent removal of the metal and cleavage of the