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Asymmetric Organocatalytic C-C Bond Forming Reactions with Organoboron Compounds: A Mechanistic Survey
(Wiley VCH Verlag, 2019-05-26)
The recent development of asymmetric organocatalytic C-C bond forming reactions involving organoboranes has attracted big interest in the synthetic community. Asymmetric organocatalytic additions to enones, aldehydes, ...
Computational characterization of the role of the base in the Suzuki-Miyaura cross-coupling reaction
(Amer Chemical SocWashingtonEUA, 2005)
Selective Oxidations of Organoboron Compounds Catalyzed by Baeyer-Villiger Monooxygenases
(WILEY-BLACKWELL, 2011)
The applicability of Baeyer-Villiger monooxygenases (BVMOs) in organoboron chemistry has been explored through testing chemo-and enantioselective oxidations of a variety of boron-containing aromatic and vinylic compounds. ...
Asymmetric synthesis of: Trans -4,5-disubstituted γ-butyrolactones involving a key allylboration step. First access to (-)-nicotlactone B and (-)-galbacin
(Royal Society of Chemistry, 2018-02)
An efficient asymmetric synthesis of trans-4,5-disubstituted γ-butyrolactones from aldehydes and enantioenriched γ-carbamate alkenylboronates is reported. The cornerstone of this strategy is the implementation of sequential ...
Remarkable reactivity of boron-substituted furans in the Diels-Alder reactions with maleic anhydride
(American Chemical Society, 2019-06-19)
The reactivity of boron-substituted furans as dienes in the Diels-Alder reaction with maleic anhydride has been investigated. Gratifyingly, the furans with boryl substituents at C-3 gave the exo cycloadduct exclusively ...
Alkylhalovinylboranes: a new class of Diels-Alder dienophiles
(Royal Society of Chemistry, 2018-10)
The Diels-Alder reactions of alkylhalovinylboranes have been investigated theoretically and experimentally. Alkylhalovinylboranes presented higher reactivity than the corresponding dialkylvinylboranes. Although endo/exo ...
Computational study of the transmetalation process in the Suzuki-Miyaura cross-coupling of aryls
(Elsevier Science SaLausanneSuíça, 2006)