Controlling the position of the nucleophilic ring-opening of 2-EWG-substituted azetidinium salts with fluoride by the N-1-(1-naphthyl)ethyl substituent and BINAM-derived bis-urea organocatalyst-Reference-Cited by-同舟云学术

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Controlling the position of the nucleophilic ring-opening of 2-EWG-substituted azetidinium salts with fluoride by the N-1-(1-naphthyl)ethyl substituent and BINAM-derived bis-urea organocatalyst

Published:2024-09 Issue: Volume: Page:134274
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Tayama Eiji^ORCID,Tsutsumi Ryoga,Uraguchi Daisuke

Publisher

Elsevier BV

Reference57 articles.

1. .

2. Stereo- and Enantioselective Addition of Organolithiums to 2-Oxazolinylazetidines as a Synthetic Route to 2-Acylazetidines;Musci;Front. Chem.,2019

3. Synthesis of spirocyclopropyl γ-lactams by tandem intramolecular azetidine ring-opening/closing cascade reaction: synthetic and mechanistic aspects;Nocquet;Tetrahedron,2012

4. Enantioselective addition of alkynylzinc to arylaldehydes catalyzed by azetidino amino alcohols bearing an additional stereogenic center;Niu;Tetrahedron: Asymmetry,2009

5. Preparation of enantiopure 2-acylazetidines and their reactions with chloroformates;Ma;Tetrahedron Lett,2007

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