Allenylidene Induced 1,2?Metalate Rearrangement of Indole?Boronates: Diastereoselective Access to Highly Substituted Indolines

نویسندگان

چکیده

A process to achieve 1,2-metalate rearrangements of indole boronate as a way access substituted indolines in high diastereoselectivities is presented. The reaction involves the generation Cu–allenylidene, which sufficiently electrophilic induce rearrangement. scope evaluated well further transformations product.

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

Pyrrolyl substituted allenylidene complexes of ruthenium.

Pyrrolyl and indolyl substituted allenylidene complexes of ruthenium have been prepared from the trapping of cationic trans-[Cl(dppm)(2)Ru=C=C=C=CH(2)](+) with various pyrroles or N-methylindole. The reaction is rationalized as involving regioselective attack of the organometallic electrophile on the electron-rich heterocycle followed by proton migration to the terminal =CH(2) entity of the int...

متن کامل

Highly diastereoselective samarium diiodide induced cyclizations of new 3-substituted indole derivatives.

Herein, we describe the synthesis of new functionalized tricyclic and tetracyclic indole derivatives via samarium diiodide induced ketyl cyclizations. The intermediate samarium organyls were either protonated using different proton sources or alkylated with various electrophiles in a highly diastereoselective manner. The obtained products were subjected to further transformations leading to syn...

متن کامل

Diastereoselective diaza-Cope rearrangement reaction.

Steric effect is used to obtain a highly diastereoselective rearrangement reaction.

متن کامل

Preparation of silyl substituted crotylzinc reagents and their highly diastereoselective addition to carbonyl compounds.

Readily prepared beta-silyl substituted crotylzinc reagents undergo highly selective allylation of carbonyl compounds leading to syn-homoallylic alcohols.

متن کامل

Highly enantioselective synthesis of chiral 3-substituted indolines by catalytic asymmetric hydrogenation of indoles.

[reaction: see text] N-Tosyl 3-substituted indoles were hydrogenated with high enantioselectivities (95-98% ee) by use of a trans-chelating chiral bisphosphine, (S,S)-(R,R)-PhTRAP ligand. The chiral catalyst, which was generated in situ from [Rh(nbd)(2)]SbF(6), PhTRAP, and Cs(2)CO(3), is useful for enantioselectively synthesizing a range of diverse optically active indolines possessing a chiral...

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: Angewandte Chemie

سال: 2021

ISSN: ['1521-3773', '1433-7851', '0570-0833']

DOI: https://doi.org/10.1002/anie.202103108