Asymmetric 1,2‐Carbamoyl Rearrangement of Lithiated Chiral Oxazolidine Carbamates and Diastereoselective Synthesis of α‐Hydroxy Amides-Reference-Cited by-同舟云学术

Asymmetric 1,2‐Carbamoyl Rearrangement of Lithiated Chiral Oxazolidine Carbamates and Diastereoselective Synthesis of α‐Hydroxy Amides

Published:2022-06-14 Issue:43 Volume:28 Page:
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chemistry A European J

Author:

Ghosh Arun K.¹^ORCID,Basu Amartyo J.¹,Hsu Che‐Sheng¹,Yadav Monika¹

Affiliation:

1. Department of Chemistry and Department of Medicinal Chemistry and Molecular Pharmacology Purdue University 560 Oval Dr. West Lafayette IN 47907 USA

Funder

Foundation for the National Institutes of Health

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202200941

Reference41 articles.

1. The Homoaldol Reaction, or How to Overcome Problems of Regio- and Stereo-selectivity

2. Die Homoaldol-Reaktion oder wie man Probleme der Regio- und Stereoselektivität in den Griff bekommt

3. Lithiated AllylN,N-Dialkylcarbamates as Homoenolate Equivalents; Synthesis of Protected 4-Oxoalkanoates

4. LithiierteN,N-Dialkylcarbamidsäure-allylester als Homoenolat-Äquivalente; Synthese geschützter 4-Oxoalkansäureester

5. Metallierte Stickstoff‐Derivate der Kohlensäure in der organischen Synthese, XXVII. – Homoaldol‐Reaktion, VII. Lithiierung acyclischer N , N ‐Dialkylcarbamidsäure‐2‐alkenylester; Silylierung und γ‐selektive α‐Hydroxyalkylierung von Homoenolat‐Reagenzien

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1. From intramolecular cyclization to intermolecular hydrolysis: TMSCF₂Br-enabled carbonylation of aldehydes/ketones and amines to α-hydroxyamides;Organic Chemistry Frontiers;2023

2. Passerini Reaction to Access α‐Hydroxy Amides by Facile Decarbonylation/Decarboxylation of Oxalic Acid;European Journal of Organic Chemistry;2022-12-20