Pyrrolidine and Piperidine Formation via Copper(II) Carboxylate Promoted Intramolecular Carboamination of Unactivated Olefins: Diastereoselectivity and Mechanism.

ChemInform
doi 10.1002/chin.200737119
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Wiley

Related search

Carboamination of Unactivated Alkenes via Three-Component Radical Conjugate Addition

Angewandte Chemie - International Edition
CatalysisChemistry
2019English

Carboamination of Unactivated Alkenes via Three‐Component Radical Conjugate Addition

Angewandte Chemie
2019English

Protecting-Group-Free Route to Hydroxylated Pyrrolidine and Piperidine Derivatives Through Cu(I)-Catalyzed Intramolecular Hydroamination of Alkenes

Synlett
Organic Chemistry
2010English

Calcium(II)- And Triflimide-Catalyzed Intramolecular Hydroacyloxylation of Unactivated Alkenes in Hexafluoroisopropanol

English

Intramolecular Asymmetric Desymmetrization via Copper Catalysis

Synfacts
2014English

Pyridine-Enabled Copper-Promoted Cross Dehydrogenative Coupling of C(sp2)–H and Unactivated C(sp3)–H Bonds

Chemical Science
Chemistry
2015English

Mechanism and Diastereoselectivity of Aziridine Formation From Sulfur Ylides and Imines: A Computational Study

English

A Simple and Efficient Synthesis of Dibenzothiophene via BF3·OEt2-Promoted Intramolecular Annulation

Synlett
Organic Chemistry
2013English

Gas Liquid Chromatographic Determination of Pyrrolidine and Piperidine in Canned Fish Products.

Nippon Suisan Gakkaishi
Aquatic Science
1991English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy