dl-selective reductive coupling/Dieckmann condensation sequence of α,β-unsaturated amides with samarium(II) iodide/HMPA. Synthesis of a new ligand, trans-1,2-cyclopentanediyl-2,2′-biphenol-Reference-Cited by-同舟云学术

dl-selective reductive coupling/Dieckmann condensation sequence of α,β-unsaturated amides with samarium(II) iodide/HMPA. Synthesis of a new ligand, trans-1,2-cyclopentanediyl-2,2′-biphenol

Published:1996-11 Issue:47 Volume:37 Page:8505-8506
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kanemasa Shuji,Yamamoto Hidetoshi,Kobayashi Shigeru

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference12 articles.

1. Synthesis of pure enantiomers of a new diol ligand, trans-4,5-Bis(2-hydroxyphenyl)-2,2-dimethyl-1,3-dioxolane

2. Yamamoto, H.; Kobayashi, S.; Kanemasa, S. Unpublished results

3. Selective Conjugate Reduction of α,β-Unsaturated Esters and AmidesviaSmI2-Promoted Electron Transfer Process

4. A facile reductive dimerization of conjugated acid derivatives with samarium diiodide

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