A convenient synthesis of 3,4-cis-disubstituted pyrrolidin-2-ones-Reference-Cited by-同舟云学术

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A convenient synthesis of 3,4-cis-disubstituted pyrrolidin-2-ones

Published:2015-01 Issue:1 Volume:56 Page:98-100
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Arfaoui Aïcha,Saâdi Fatma,Smida Youssef Ben,Arfaoui Youssef,Nefzi Adel,Amri Hassen

Funder

Higher Education and Scientific Research of Tunisia

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference50 articles.

1. The stereocontrolled synthesis of enantiopure α-methano heterocycles and constrained amino acid analogs

2. The influence of benzylic protection and allylic substituents on the CuCl-TMEDA catalyzed rearrangement of N-allyl-N-benzyl-2,2-dihaloamides to γ-lactams. Application to the stereoselective synthesis of pilolactam

3. A convenient approach to diastereomerically pure 1,3,4-trisubstituted pyrrolidin-2-ones by intramolecular cyclisation of N-(2-alken-1-yl)amides mediated by Mn(III). An entry to both (R)- and (S)-3-pyrrolidineacetic acid

4. Stereospecific synthesis of 4-alkylglutamates and 4-alkylprolines

5. Synthesis and antihypertensive activity of 4-(1,2-dihydro-2-oxo-1-pyridyl)-2H-1-benzopyrans and related compounds, new potassium channel activators

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1. Joint Experimental/Theoretical Investigation of the Chemoselective Iridium(III) Metallacycle-Catalyzed Reduction of Substituted γ-Lactams by Et₃SiH;Organometallics;2024-04-25

2. Atom-transfer radical cyclization of α-bromocarboxamides under organophotocatalytic conditions;Tetrahedron Letters;2021-04

3. Synthesis Methods in Solid-State Chemistry;Synthesis Methods and Crystallization;2020-10-07

4. One-Pot Three-Component Synthesis of Pyrrolidin-2-ones via a Sequential Wittig/Nucleophilic Addition/Cyclization Reaction;Synthesis;2019-03-04

5. Crystal structure of methyl 1-(4-fluorobenzyl)-4-methoxy-5-oxopyrrolidine-3-carboxylate, C14H16FNO4;Zeitschrift für Kristallographie - New Crystal Structures;2017-09-26

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