A NEW AND CONVENIENT ROUTE TO THE AMIDES OF α-AMINO ACIDS AND α-HYDROXY ACIDS BY MEANS OF THE PALLADIUM CATALYZED FACILE CLEAVAGE OF 3-SUBSTITUTED-4-ARYLAZETIDIN-2-ONES-Reference-Cited by-同舟云学术

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A NEW AND CONVENIENT ROUTE TO THE AMIDES OF α-AMINO ACIDS AND α-HYDROXY ACIDS BY MEANS OF THE PALLADIUM CATALYZED FACILE CLEAVAGE OF 3-SUBSTITUTED-4-ARYLAZETIDIN-2-ONES

Published:1980-07-05 Issue:7 Volume:9 Page:853-856
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Ojima Iwao,Suga Shigemi,Abe Rumiko

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference5 articles.

1. Synthetic routes to β-lactams

2. β-Lactams: retrospect and prospect

3. .beta.-Lactams. XXXVI. Monocyclic cis .beta.-lactams via penams and cephams

4. Ueber eine neue Synthese des Tyrosins

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1. Asymmetric Synthesis of β-Lactams by the Staudinger Reaction;Organic Reactions;2018-04-04

2. Evidence for an umpolung type of [2+2] cycloaddition of 2-carbamoyl ketenes;New Journal of Chemistry;2017

3. The stereoselective formation of β-lactams with acyl ketenes generated from 5-acyl-Meldrum's acids;New Journal of Chemistry;2016

4. Identification, isolation and characterization of process related impurities in ezetimibe;Journal of Pharmaceutical and Biomedical Analysis;2014-01

5. Synthesis of 3-Carbamoylβ-LactamsviaManganese(III)-Promoted Cyclization ofN-Alkenylmalonamides;Helvetica Chimica Acta;2013-11

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