Reaction of 5-aryloxazolidines with arylmagnesium bromides as a new route to N-benzyl-β-hydroxyphenethylamines as starting materials for the preparation of 4-aryl-1,2,3,4-tetrahydroisoquinolines-Reference-Cited by-同舟云学术

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Reaction of 5-aryloxazolidines with arylmagnesium bromides as a new route to N-benzyl-β-hydroxyphenethylamines as starting materials for the preparation of 4-aryl-1,2,3,4-tetrahydroisoquinolines

Published:2013-05 Issue:21 Volume:54 Page:2699-2702
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Moshkin Vladimir S.,Sosnovskikh Vyacheslav Ya.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 articles.

1. Some 1,2,3,4-tetrahydroisoquinoline alkaloids of the 1-benzylisoquinoline group;Shklyaev,2011

2. Cherylline, a 4-phenyl-1,2,3,4-tetrahydroisoquinoline alkaloid

3. Latifine, a biogenetic isomer of cherylline, from Crinum latifolium L.

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2. Ring-opening of oxazolidines with acetone cyanohydrin: A short and effective pathway to 2-((2-hydroxyethyl)amino)acetonitriles from carbonyl compounds;Tetrahedron Letters;2024-01

3. Accessing N‐Propargyl Amino Alcohols through Cu(I)‐Catalyzed A ³ ‐Coupling/Annulation and Bi(III)‐Promoted Ring‐Opening;ChemistrySelect;2022-02-17

4. Reactions of 5-aryloxazolidines with CH-acidic compounds;Tetrahedron Letters;2019-06

5. Novel synthesis of aminoacetonitriles via the selective demethylation of quaternary ammonium salts;Tetrahedron Letters;2018-04

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