Stereoselective dibromination of diphenylphosphorylallenes with N-bromosuccinimide under mild conditions
نویسندگان
چکیده
منابع مشابه
Triphenylphosphine oxide-catalyzed stereoselective poly- and dibromination of unsaturated compounds.
A novel PPh3O catalyzed bromophosphonium salt-mediated dibromination of α,β-unsaturated esters and β,γ-unsaturated α-ketoesters has been developed. The products were obtained with good to excellent yields and excellent diastereoselectivities. This dibromination reaction is a good complement to the field of dibromination.
متن کاملSelective conversion of alcohols and phenols to tetrahydropyranyl ethers catalyzed with N-chlorosaccharin under mild and solvent-free conditions
An efficient method is described for the mild and rapid tetrahydropyranylation of alcohols and phenols using a catalytic amount of N-chlorosaccharin (1 mol %) and 3, 4-dihydro-2H-pyran under solvent-free condition at room temperature. Benzylic alcohols and phenols containing electron withdrawing or donating groups in various positions of phenyl ring, cinamyl alcohol, primary, ...
متن کاملSelective conversion of alcohols and phenols to tetrahydropyranyl ethers catalyzed with N-chlorosaccharin under mild and solvent-free conditions
An efficient method is described for the mild and rapid tetrahydropyranylation of alcohols and phenols using a catalytic amount of N-chlorosaccharin (1 mol %) and 3, 4-dihydro-2H-pyran under solvent-free condition at room temperature. Benzylic alcohols and phenols containing electron withdrawing or donating groups in various positions of phenyl ring, cinamyl alcohol, primary, ...
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A stereoselective one-pot procedure was developed to prepare S-substituted (Z)-enol esters through a base-triggered rearrangement. This transition metal-free multicomponent approach can be performed under an air atmosphere at room temperature, tolerates a wide set of chemical functionalities and generally affords high isolated yields. The (Z)-selectivity arises from the [1,4]-S- to O-acyl migra...
متن کاملKOtBu-mediated stereoselective addition of quinazolines to alkynes under mild conditions.
A facile alkenylation of quinazolines with unactivated terminal alkynes has been achieved in the presence of KOtBu without the aid of any transition metal catalysts. The reaction is carried out under very mild conditions and shows a high stereoselectivity. A possible radical-based mechanism is also explored.
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ژورنال
عنوان ژورنال: Journal of Saudi Chemical Society
سال: 2018
ISSN: 1319-6103
DOI: 10.1016/j.jscs.2017.10.007