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Literature DB >> 19082143

Enamides: valuable organic substrates.

Abstract

Enamides display a fine balance of stability and reactivity, which is now leading to their increasing use in organic synthesis. Enamides offer multiple opportunities for the inclusion of nitrogen based functionality into organic systems. Recent examples of these compounds as substrates are discussed in this article.

Entities: Chemical

Year: 2008 PMID： 19082143 DOI： 10.1039/b809319a

Source DB: PubMed Journal: Org Biomol Chem ISSN： 1477-0520 Impact factor: 3.876

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Cited

28 in total

1. A tandem 1,3-H-shift-6π-electrocyclization-cyclic 2-amido-diene intramolecular Diels-Alder cycloaddition approach to BCD-Ring of atropurpuran.

Authors: Ryuji Hayashi; Zhi-Xiong Ma; Richard P Hsung
Journal: Org Lett Date: 2011-12-13 Impact factor: 6.005

2. Torquoselective ring closures of chiral amido trienes derived from allenamides. A tandem allene isomerization-pericyclic ring-closure-intramolecular Diels-Alder cycloaddition.

Authors: Ryuji Hayashi; John B Feltenberger; Richard P Hsung
Journal: Org Lett Date: 2010-03-19 Impact factor: 6.005

Review 3. Catalytic asymmetric cycloaddition reactions of enoldiazo compounds.

Authors: Kostiantyn O Marichev; Michael P Doyle
Journal: Org Biomol Chem Date: 2019-04-24 Impact factor: 3.876

4. A highly regio- and stereoselective synthesis of α-fluorinated imides via fluorination of chiral enamides.

Authors: Yan-Shuang Xu; Yu Tang; He-Jing Feng; Ji-Tian Liu; Richard P Hsung
Journal: Org Lett Date: 2015-01-12 Impact factor: 6.005

5. A highly stereoselective Diels-Alder cycloaddition of enones with chiral cyclic 2-amidodienes derived from allenamides.

Authors: Li-Chao Fang; Richard P Hsung; Zhi-Xiong Ma; William R Presser
Journal: Org Lett Date: 2013-09-03 Impact factor: 6.005

Review 6. Cycloaddition reactions of enoldiazo compounds.

Authors: Qing-Qing Cheng; Yongming Deng; Marianne Lankelma; Michael P Doyle
Journal: Chem Soc Rev Date: 2017-08-29 Impact factor: 54.564

7. Enamide-benzyne-[2 + 2] cycloaddition: stereoselective tandem [2 + 2]-pericyclic ring-opening-intramolecular N-tethered [4 + 2] cycloadditions.

Authors: John B Feltenberger; Ryuji Hayashi; Yu Tang; Eric S C Babiash; Richard P Hsung
Journal: Org Lett Date: 2009-08-20 Impact factor: 6.005