Search

Enantioenriched spiroindoles are highly efficiently obtained by iridium-catalyzed asymmetric allylic dearomatization and reduction. [ABSTRACT FROM AUTHOR]

This is the first example using multisubstituted pyrroles as substrates in asymmetric allylic alkylation reactions. [ABSTRACT FROM AUTHOR]

The article presents chemical equations to the article "Enantioselective Synthesis of N-Allylindoles via Palladium-Catalyzed Allylic Amination/Oxidation of Indolines" by Q. Zhao and others published in "RSC Advances" in 2014.

Review: 72 refs. [ABSTRACT FROM AUTHOR]

The asymmetric cyclization reaction of 2-indolyl allyl carbonates gives excellent chemo- and enantioselectivities and can be conducted under mild conditions. [ABSTRACT FROM AUTHOR]

This is the first Pd-catalyzed intermolecular asymmetric allylic dearomatization of β-naphthol derivatives yielding products with all-carbon quaternary stereocenters with good enantioselectivities. [ABSTRACT FROM AUTHOR]

A chemical diagram is presented that depicts the enantioselective functionalization of indoles and pyrroles using an in situ formed spiro intermediate.

Review: 91 refs. [ABSTRACT FROM AUTHOR]

The article presents the asymmetric intramolecular allylic amination reaction catalyzed by iridium(I) N-heterocyclic carbene complex.

The diagrams of the chemical equation for the Chiral Five-Membered Aza-Spiroindolenines is presented, with the methods of stereoselective migration reactions and synthesis.

Abstract: This protocol provides facile access to functionalized β—naphthalenone compounds with a chiral quaternary carbon center in excellent yields and enantioselectivity. [ABSTRACT FROM AUTHOR]