1218988-13-6Relevant articles and documents
Highly diastereo- and enantioselective allylboration of aldehydes using α-substituted allyl/crotyl pinacol boronic esters via in situ generated borinic esters
Chen, Jack L.-Y.,Scott, Helen K.,Hesse, Matthew J.,Willis, Christine L.,Aggarwal, Varinder K.
, p. 5316 - 5319 (2013/05/21)
Readily available, α-substituted allyl/crotyl pinacol boronic esters often give low E/Z selectivity (with Z favored) in reactions with aldehydes. We found that addition of nBuLi to the pinacol boronic ester followed by trapping of the alkoxide with TFAA leads to an intermediate allyl borinic ester which undergoes allylboration with very high E selectivity. The substrate scope includes primary to tertiary alkyl α-substituents, crotyl substrates, and the previously unreported β-methallyl pinacol boronic esters. The latter give very high Z selectivity under standard conditions which is completely reversed to high E selectivity under the new conditions. Monitoring the reaction by 11B NMR confirmed that the reaction proceeds through a borinic ester intermediate.
Erratum: Application of the lithiation-borylation reaction to the preparation of enantioenriched allylic boron reagents and subsequent in situ conversion into 1,2,4-trisubstituted homoallylic alcohols with complete control over all elements of stereochemi
Althaus, Martin,Mahmood, Adeem,Suarez, Jose Ramon,Thomas, Stephen P.,Aggarwal, Varinder K.
supporting information; experimental part, p. 5922 - 5922 (2010/07/05)
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