An Efficient Synthesis of 3-tert-Aminopropanol Derivatives by Regioselective Ring Opening of Tetrahydro-1,3-oxazines with Grignard Reagents
Author:
Affiliation:
1. a Departamento de Química Orgánica, Facultad de Ciencias , Universidad de Valladolid , 47011, Valladolid, Spain
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397919008052822
Reference20 articles.
1. Diphenylethylamines. I. The Preparation of Tertiary Amines by the Grignard Reaction1,2
2. Synthesis and Reactions of α-Dialkylaminobenzyl Butyl Ethers. Interactions with Grignard Reagents to Form Tertiary Amines1
3. Vinyl-copper derivatives XII : Stereospecific synthesis of allylic amines by aminomethylation of organocopper reagents
4. Studies on Acetylenic Compounds. XXXIII. A New Synthetic Method for Aminoacetylenic Compounds.
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