61674-93-9Relevant academic research and scientific papers
A simple, nontoxic iron system for the allylation of zinc enolates
Jarugumilli, Gopala K.,Cook, Silas P.
, p. 1904 - 1907 (2011)
Diiron nonacarbonyl in combinationwith triphenylphosphine has been identified as a low-cost and environmentally benign catalyst system for the allylation of zinc enolates generated in situ from copper-catalyzed asymmetric conjugate addition reactions. The
Enantioselective synthesis of bicyclic compounds via catalytic 1,4-addition-ring closing metathesis
Naasz,Arnold,Minnaard,Feringa
, p. 735 - 736 (2007/10/03)
A novel three step asymmetric annulation procedure comprises a tandem catalytic enantioselective 1,4-additionallylic substitution, Grignard addition and ring closing metathesis (RCM) sequence to provide [6,6], [7,6], [8,6] and [6,7] bicyclic products with
Radical α-Allylation of Alkyl-Substituted α-(Phenylseleno)cycloalkanones
Toru, Takeshi,Okumura, Tatsuya,Ueno, Yoshio
, p. 1277 - 1280 (2007/10/02)
Irradiation and thermal reaction of 3-, 4-, or 6-alkyl-2-(phenylseleno)cycloalkanones with tributyl-2-propenyltin gave 2-allylated products in high yields.Either trans- or cis-selenocycloalkanones afforded the identical distribution of cis- and trans-ally
