Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Iron, tricarbonyl acylation alkylation

Cyclopropanation reactions of nonheteroatom-stabilized carbenes have also been developed. The most versatile are the cationic iron carbenes that cyclopropanate alkenes with high stereospecificity under very mild reaction conditions. The cyclopropanation reagents are available from a number of iron complexes, for example, (9-alkylation of cyclopentadienyl dicarbonyliron alkyl or acyl complexes using Meerwein salts affords cationic Fischer carbenes. Cationic iron carbene intermediates can also be prepared by reaction of CpFe(CO)2 with aldehydes followed by treatment with TMS-chloride. Chiral intermolecular cyclopropanation using a chiral iron carbene having a complexed chromium tricarbonyl unit is observed (Scheme 61). [Pg.3230]


See other pages where Iron, tricarbonyl acylation alkylation is mentioned: [Pg.192]    [Pg.385]    [Pg.111]    [Pg.683]    [Pg.399]   
See also in sourсe #XX -- [ Pg.706 , Pg.707 , Pg.708 ]

See also in sourсe #XX -- [ Pg.4 , Pg.706 , Pg.707 , Pg.708 ]

See also in sourсe #XX -- [ Pg.4 , Pg.706 , Pg.707 , Pg.708 ]




SEARCH



Acyls alkylation

Alkylation tricarbonyls

Iron alkyls

Iron, tricarbonyl acylation

© 2024 chempedia.info