α-Amination of keto-nitrones via Multihetero-Cope rearrangement employing an imidoyl chloride reagent

نویسندگان
چکیده

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

α-Amination of keto-nitrones via multihetero-Cope rearrangement employing an imidoyl chloride reagent.

α-Aminations of ketone-derived nitrones have been developed via [3,3]-rearrangement of the intermediates generated upon condensation with imidoyl chlorides. Careful reagent selection provides synthetically attractive amino protecting groups. The enediamide or α'-carbamoyl enamide products can be hydrolyzed to the desired carbonyl, or exposed to electrophiles for further α-functionalization.

متن کامل

Gold-catalyzed 1,2-iminonitronation of electron-deficient alkynes with nitrosoarenes to afford α-imidoyl nitrones.

Gold-catalyzed 1,2-iminonitronation of propiolate derivatives with nitrosoarenes to give α-imidoyl nitrones is described; this new reaction is applicable to diverse propiolate derivatives and nitrosoarenes.

متن کامل

BET & ELF Quantum Topological Analysis of Neutral 2-Aza-Cope Rearrangement of γ-Alkenyl Nitrones.

The 2-Aza-Cope rearrangement of γ-alkenyl nitrones is a rare example of the neutral thermal 2-aza-Cope process that usually takes place with cationic species. During the rearrangement, a redistribution of bonds and electronic density occurs in one kinetic step. However, the introduction of substituents with different steric requirements and electronic features might alter the activation energie...

متن کامل

Antarafacial-Antarafacial Cope Rearrangement

Thermal rearrangement of 2-thiabicyclo[ 3.2.0]hepta-3,6-diene-6,7-dicarbonitriles 1-3 to their 4,5-dicarbonitrile isomers 4-6 takes place at 110-140 "C in yields of 82-84%. The reactions are first order with rates almost independent of the polarity of the solvent. Activation parameters (m = 120-140 kJ mol-' and AS* = 0 J K-l mol-') are in agreement with a concerted symmetry-allowed antarafacial...

متن کامل

Asymmetric α-amination of β-keto esters using a guanidine–bisurea bifunctional organocatalyst

An asymmetric α-amination of β-keto esters with azodicarboxylate in the presence of a guanidine-bisurea bifunctional organocatalyst was investigated. The α-amination products were obtained in up to 99% yield with up to 94% ee.

متن کامل

ذخیره 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: Chemical Communications

سال: 2012

ISSN: 1359-7345,1364-548X

DOI: 10.1039/c2cc33401a