Synthetic Studies on the Role of Substituents at C-3 Position on C3-C4 Bond Cleavage of β-Lactam Ring: Convenient Route for Diastereoselective Synthesis of Pyridin-2-ones-Reference-Cited by-同舟云学术

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Synthetic Studies on the Role of Substituents at C-3 Position on C3-C4 Bond Cleavage of β-Lactam Ring: Convenient Route for Diastereoselective Synthesis of Pyridin-2-ones

Published:2012 Issue:2 Volume:86 Page:1301
ISSN:0385-5414
Container-title:HETEROCYCLES
language:en
Short-container-title:HETEROCYCLES

Author:

P. Mahajan Mohinder,Singh Pardeep,Singh Parvesh,Kumar Kewal,Kumar Vipan,Bisetty Krishna

Publisher

The Japan Institute of Heterocyclic Chemistry

Subject

Organic Chemistry,Pharmacology,Analytical Chemistry

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recent Progress in Chemistry of β-Lactams;Mini-Reviews in Organic Chemistry;2019-08-27

2. Intramolecular [2 + 2] Cycloadditions of Alkyl(phenylthio)ketenes: Total Synthesis of (+)-Sphaerodiol;Organic Letters;2018-03-13

3. Synthetic Approaches toward Monocyclic 3-Amino-β-lactams;ChemistryOpen;2017-06

4. Triflic acid promoted fries rearrangement of C-3 vinyl/isopropenyl-azetidin-2-ones: single-pot synthesis of C-3 functionalized-2-aryl-2,3-dihydro-quinoline-4(1H)-ones;RSC Adv.;2014

5. ChemInform Abstract: Synthetic Studies on the Role of Substituents at C-3 Position on C3-C4 Bond Cleavage of β-Lactam Ring: Convenient Route for Diastereoselective Synthesis of Pyridin-2-ones.;ChemInform;2013-04-11

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