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

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

Research output: Contribution to journal › Article › peer-review

DOI

https://doi.org/10.1016/j.tetlet.2013.03.076
Final published version

Original language	English
Pages (from-to)	2699-2702
Number of pages	4
Journal	Tetrahedron Letters
Volume	54
Issue number	21
DOIs	https://doi.org/10.1016/j.tetlet.2013.03.076
Publication status	Published - 22 May 2013

Research areas

4-Aryl-1,2,3,4-tetrahydroisoquinolines, 5-Aryloxazolidines, Non-stabilized azomethine ylide, [3+2] Cycloaddition, Cyclization reaction, ONE-POT SYNTHESIS, DOPAMINE D-1, CHERYLLINE, TETRAHYDROISOQUINOLINES, (&/-)-CHERYLLINE, REARRANGEMENT, DERIVATIVES, CYCLIZATION

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

WoS ResearchAreas Categories

Chemistry, Organic

ID: 909503