KeteneN,S-acetals in heterocyclic synthesis: Part 1: Synthesis ofN-phenyl-2-ylidene and 2,5-diylidene-4-thiazolidinone derivatives-Reference-Cited by-同舟云学术

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KeteneN,S-acetals in heterocyclic synthesis: Part 1: Synthesis ofN-phenyl-2-ylidene and 2,5-diylidene-4-thiazolidinone derivatives

Published:2007-10-29 Issue:6 Volume:28 Page:563-572
ISSN:1741-5993
Container-title:Journal of Sulfur Chemistry
language:en
Short-container-title:Journal of Sulfur Chemistry

Author:

Farhat M. F.¹,El-Saghier A. M. M.²,Makhlouf M. A.¹,Kreddan K. M.³,Elmezoughi A. B.¹

Affiliation:

1. a Chemistry Department, Faculty of Science , Al-Fateh University , PO Box 13494, Tripoli, Libya

2. b Chemistry Department, Faculty of Science , Seventh of April University , Al-Zawia, Libya

3. c Libyan Petroleum Institute , PO Box 3064, Tripoli, Libya

Publisher

Informa UK Limited

Subject

General Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/17415990701586823

Reference38 articles.

1. α-Oxoketene-S,S-, N,S- and N,N-acetals: Versatile intermediates in organic synthesis

2. The RegiospecificN-Alkylation of Heterocyclic Ketene Aminals with Ethyl Bromoacetate: A Facile Route to 3-Pyrrolidinone Fused Diazaheterocycles

3. Reaction of Heterocyclic Ketene Aminals with α-Bromoketones: A Convenient Synthesis of Pyrrole-Fused 1,3-Diazaheterocycles

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1. Unexpected products using Biginelli reaction: Synthesis, antimicrobial potency, docking simulation, and DFT investigations of some new amidopyridines;Journal of Molecular Structure;2024-01

2. Synthesis, Biological Evaluation, and in-Silico Molecular Docking Studies of Multifunctional Thiazolidine Derivatives;Polycyclic Aromatic Compounds;2023-08-02

3. Tandem synthesis and antibacterial screening of novel thieno[2,3-b]thiophene-linked bis(thiazole) hybrids;Synthetic Communications;2021-04-27

4. Synthesis, X-ray analysis and computational studies of two novel thiophene derivatives;Journal of Sulfur Chemistry;2020-05-25

5. Applications of alkyl orthoesters as valuable substrates in organic transformations, focusing on reaction media;RSC Advances;2020

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