215957-65-6Relevant articles and documents
Palladium-catalyzed diastereo- and enantioselective Wagner-Meerwein shift: Control of absolute stereochemistry in the C-C bond migration event
Trost, Barry M.,Xie, Jia
, p. 6231 - 6242 (2008/12/20)
Inducing absolute stereochemistry in Wagner-Meerwein shifts was examined in a ring expansion protocol. Initiated by generation of a π-allylpalladium intermediate by hydropalladation of allenes, the ring expansion of allenylcyclobutanol substrates proceeded with excellent diastereo- and enantioselectivities. The results demonstrate that, during the C-C bond migration process, our chiral catalysts can control the stereochemistry of both the π-allylpalladium intermediate and the corresponding migration bond. Moreover, the stereochemical outcome of the reaction can be rationalized very well with the working model of the chiral catalyst. The method provides an efficient way to synthesize highly substituted cyclopentanones with an α-chiral O-tertiary center which has various synthetic applications.
Two-carbon ring expansion of cyclobutanone skeletons by nickel-catalyzed intermolecular alkyne insertion
Murakami, Masahiro,Ashida, Shinji,Matsuda, Takanori
, p. 7540 - 7546 (2007/10/03)
The reaction of cyclobutanone with an alkyne in the presence of a nickel(0) catalyst formally achieves intermolecular alkyne insertion between the carbonyl carbon and the α-carbon of a cyclobutanone, providing a six-membered carbocyclic skeleton.
Conformational control by quaternary centres: theory, database evidence and application to polymers
Adler, Roger W.,Allen, Paul R.,Anderson, Kevin R.,Butts, Craig P.,Khosravi, Ezat,et al.
, p. 2083 - 2108 (2007/10/03)
The conformational effects of the quaternary centre in (RCH2CH2)4Xq species are studied by molecular mechanics calculations on hydrocarbons, ammonium ions, and related species, and the results verified by data on quaternary ammonium ions from the Cambridge Structural Database. Prn4C and Prn4N+ have just two low-energy structures, with D2d or S4 symmetry. All other conformations suffer from g+g- non-bonding interactions and will be populated to the extent of q-CH2 and the next set of torsions, -CH2-CH2-CH2-Xq, but the third set of torsions away from the quaternary centre is unaffected. Two competitive mechanisms for interconversion of the D2d and S4 conformations are proposed on the basis of molecular mechanics calculations. Polymers [(RCH2CH2)2C(CH2)2]n and [(RCH2CH2)2C(CH2)3]n are strain-free with controlled conformations for the -(CH2)2- and -(CH2)3- segments. In polymers containing simple alkyl side chains, there are two energetically similar conformations associated with the D2d local structure which have aaaa and ag+/-g+/-a torsion angle sequences for the polymer chain, and two comparable sequences ag+/-aa and ag+/-g+/-a associated with S4 local symmetry. Poly[(1,1-di-R)butane-1,4-diyl]s (R=Et,Pr,Bu and PhCH2CH2) have been prepared by ring opening metathesis polymerisation of 3,3-dialkylcyclobutenes, followed by diimide reduction, and their physical properties are in accord with these predictions. More highly structured side groups can act as extra conformational control elements, and the preparation of monomers and some polymers with these extra features is reported. Planar aromatic side groups like fluorene favour aaaa conformations, cyclohexyl side groups disfavour aaaa, but do not strongly discriminate between ag+/-aa and ag+/-g+/-a, adamantane side groups strongly favour ag+/-g+/-a, and a chiral ag+aa sequence is favoured for a polymer from (1R,2R,5R,7R)-2,8,8-trimethyltricyclo[5.1.1.02,5]non-3-ene, itself derived from α-pinene. Studies directed at preparing some structurally-related ketal polymers and a potential covalent ketal network are also described.
