Zhao, Wei published the artcileRemote Stereocenter through Amide-Directed, Rhodium-Catalyzed Enantioselective Hydroboration of Unactivated Internal Alkenes, Application of cis-3,7-Dimethyl-2,6-Octadien-1-Ol, the publication is Journal of the American Chemical Society (2022), 144(29), 13071-13078, database is CAplus and MEDLINE.
Despite the frequent occurrence of γ-branched amines in bioactive mols., the direct catalytic asym. synthesis of this structural motif containing a remote stereocenter remains an important synthetic challenge. Here, authors report an amide-directed, rhodium-catalyzed highly diastereo- and enantioselective hydroboration of unactivated internal alkenes. This method provided facile access to enantioenriched amines containing β,γ-vicinal stereocenters. The application of this strategy to the synthesis of bioactive mols. was demonstrated. Computational studies indicated that migratory insertion of the alkene into rhodium hydride controls the enantioselectivity.
Journal of the American Chemical Society published new progress about 106-25-2. 106-25-2 belongs to alcohols-buliding-blocks, auxiliary class Natural product, name is cis-3,7-Dimethyl-2,6-Octadien-1-Ol, and the molecular formula is C15H21BO2, Application of cis-3,7-Dimethyl-2,6-Octadien-1-Ol.
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