Lithium–Bromide Exchange Versus Nucleophilic Addition of Schiff's Base: Unprecedented Tandem Cyclisation Pathways

Chemistry - A European Journal - United Kingdom
doi 10.1002/chem.201903366
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Wiley

Related search

Lithium–Bromide Exchange Versus Nucleophilic Addition of Schiff's Base: Unprecedented Tandem Cyclisation Pathways

Chemistry - A European Journal
Organic ChemistryCatalysisChemistry
2019English

Direct N-Acetyl Enamine Formation: Lithium Bromide Mediated Addition of Methyllithium to Nitriles

English

Tandem Processes Identified From Reaction Screening: Nucleophilic Addition to ArylN-Phosphinylimines Employing La(III)-Tfaa Activation

Journal of the American Chemical Society
BiochemistryColloidCatalysisChemistrySurface Chemistry
2010English

Nucleophilic Addition of Thiols to Deoxynivalenol

Journal of Agricultural and Food Chemistry
AgriculturalChemistryBiological Sciences
2015English

Tandem Nucleophilic Addition / Fragmentation of Vinylogous Acyl Triflates: 2-Methyl-2-(1-Oxo-5-Heptynyl)-1,3-Dithiane

Organic Syntheses
Organic ChemistryTheoretical ChemistryPhysical
2011English

Unprecedented Diastereoselective Arylogous Michael Addition of Unactivated Phthalides

Chemistry - A European Journal
Organic ChemistryCatalysisChemistry
2019English

Nucleophilic Addition Γ to the Carbonyl Group

Synfacts
2009English

Reactions of Cyclopropanone Acetals With Alkyl Azides: Carbonyl Addition Versus Ring-Opening Pathways

Journal of Organic Chemistry
Organic Chemistry
2007English

Sulfinate-Engaged Nucleophilic Addition Induced Allylic Alkylation of Allenoates

English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy