Synthesis of 2,3,4,5-tetra-substituted pyrroles via a base-promoted double Michael reaction of oxime-enoates with nitroolefins-Reference-Cited by-同舟云学术

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Synthesis of 2,3,4,5-tetra-substituted pyrroles via a base-promoted double Michael reaction of oxime-enoates with nitroolefins

Published:2013-07 Issue:31 Volume:54 Page:4073-4075
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kuroda Yusuke,Imaizumi Kazuto,Yamada Ken-ichi,Yamaoka Yosuke,Takasu Kiyosei

Funder

Scientific Research and Platform for Drug Design, Discovery and Development from MEXT

Takeda Science Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference29 articles.

1. Lamellarins and Related Pyrrole-Derived Alkaloids from Marine Organisms

2. Biological formation of pyrroles: Nature's logic and enzymatic machinery

3. Chemistry and Biology of Roseophilin and the Prodigiosin Alkaloids: A Survey of the Last 2500 Years

4. Discovery of novel, non-acidic 1,5-biaryl pyrrole EP1 receptor antagonists

5. Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions

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1. Stereocontrol in Preparation of Cyclopalladated Alkylaromatic Oximes and Evaluation of Their Stereoselective Esterase-Type Catalytic Activity;Organometallics;2017-08-18

2. Regioselective Hetero-Michael Addition of Oxygen, Sulfur, and Nitrogen Nucleophiles to Maleimides Catalyzed by BF3·OEt2;Synthesis;2015-03-05

3. Microwave-Promoted Tin-Free Iminyl Radical Cyclization with TEMPO Trapping: A Practical Synthesis of 2-Acylpyrroles;Organic Letters;2015-01-16

4. One-pot highly diastereoselective annulation to N-unprotected tetrasubstituted 2-pyrrolines;Green Chemistry;2015

5. Part I: Nitroalkenes in the synthesis of heterocyclic compounds;RSC Adv.;2014-09-17

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