Catalytic Enantioselective Birch–Heck Sequence for the Synthesis of Tricyclic Structures With All-Carbon Quaternary Stereocenters

Organic Letters - United States
doi 10.1021/acs.orglett.8b00196
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Chemical Society (ACS)

Related search

Catalytic Enantioselective BirchHeck Sequence for the Synthesis of Tricyclic Structures With All-Carbon Quaternary Stereocenters

English

Catalytic Enantioselective Construction of All-Carbon Quaternary Stereocenters

Synthesis
Organic ChemistryCatalysis
2006English

Exploration of the Enantioselective Birch-Cope Sequence for the Synthesis of Carbocyclic Quaternary Stereocenters

English

Catalytic Enantioselective HouseMeinwald Rearrangement: Efficient Construction of All-Carbon Quaternary Stereocenters

English

Catalytic Enantioselective Stereoablative Alkylation of 3-Halooxindoles: Facile Access to Oxindoles With C3 All-Carbon Quaternary Stereocenters

Angewandte Chemie
2009English

Modular, Catalytic Enantioselective Construction of Quaternary Carbon Stereocenters by Sequential Cross-Coupling Reactions

Organic Letters
BiochemistryOrganic ChemistryTheoretical ChemistryPhysical
2016English

Enantioselective Syntheses of Various Chiral Multicyclic Compounds With Quaternary Carbon Stereocenters by Catalytic Intramolecular Cycloaddition

English

Catalytic Enantioselective Pinacol and Meinwald Rearrangements for the Construction of Quaternary Stereocenters

English

Cross-Dehydrogenative Coupling Enables Enantioselective Access to CF3-substituted All-Carbon Quaternary Stereocenters

Chemical Science
Chemistry
2020English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy