Protolysis of Cyclopropanes with Geminal Electronegative Substituents.
نویسندگان
چکیده
منابع مشابه
Chemistry of a geminal frustrated Lewis pair featuring electron withdrawing C6F5 substituents at both phosphorus and boron.
Hydroboration of the electron poor phosphine (1-propenyl)P(C(6)F(5))(2) with Piers' borane [HB(C(6)F(5))(2)] gave the geminal frustrated Lewis pair (C(6)F(5))(2)P-CH(Et)-B(C(6)F(5))(2). It undergoes 1,2-addition reactions to an alkene and an alkyne and to the C=N bond of an isocyanate. With mesityl azide it undergoes a 1,3-addition reaction.
متن کاملElectronegative plasma equilibria with spatially varying ionization
Electronegative inductive discharges in higher pressure ranges typically exhibit strongly localized ionization near the coil structure, with decay of the electron temperature and ionization into the central discharge region. We use a two-dimensional (2D) fluid code with a chlorine feedstock gas to determine the spatial profiles of the particle densities and electron temperature in a cylindrical...
متن کاملSynthesis of spirocycles via ring closing metathesis of heterocycles carrying gem-diallyl substituents obtained via ring opening of (halomethyl)cyclopropanes with allyltributyltin.
In the presence of allyl tri-n-butyltin--AIBN, cyclopropylmethyl bromides/xanthates undergo ring-opening reaction with concomitant formation of geminal diallyl derivatives in good yields. The ring closing metathesis reactions on geminal diallyl derivatives with Grubbs' catalyst provided spirocyclopentenyl products. Combination of these two methodologies has been applied to the synthesis of mono...
متن کاملLewis acid-promoted cycloaddition reaction of cyclopropanes with allylsilanes.
The treatment of cyclopropanes having donor and acceptor substituents at the vicinal positions on the cyclopropane ring with a Lewis acid readily generates a 1,3-zwitterion, which reacted with allylsilanes to produce cycloadducts and allylic products. It was found that the yield of the cycloadduct depends on the steric demand of the alkyl substituents on the silicon atom.
متن کاملRing Opening of Donor–Acceptor Cyclopropanes with N-Nucleo- philes
Abstract Ring opening of donor–acceptor cyclopropanes with various N-nucleophiles provides a simple approach to 1,3-functionalized compounds that are useful building blocks in organic synthesis, especially in assembling various N-heterocycles, including natural products. In this review, ring-opening reactions of donor–acceptor cyclopropanes with amines, amides, hydrazines, N-heterocycles, nitri...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Acta Chemica Scandinavica
سال: 1988
ISSN: 0904-213X
DOI: 10.3891/acta.chem.scand.42b-0345