Design, Prins-cyclization reaction promoting diastereoselective synthesis of 10 new tetrahydropyran derivatives and in vivo antinociceptive evaluations-Reference-Cited by-同舟云学术

Design, Prins-cyclization reaction promoting diastereoselective synthesis of 10 new tetrahydropyran derivatives and in vivo antinociceptive evaluations

Published:2012-12 Issue: Volume:58 Page:1-11
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Capim Saulo L.,Carneiro Paulo H.P.,Castro Paloma C.,Barros Maithê R.M.,Marinho Bruno G.,Vasconcellos Mário L.A.A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference50 articles.

1. Structurally and Stereochemically Diverse Tetrahydropyran Synthesis through Oxidative CH Bond Activation

2. Synthesis of six-membered oxygenated heterocycles through carbon–oxygen bond-forming reactions

3. A reação de ciclização de prins: uma estratégia eficiente para síntese estereosseletiva de anéis tetraidropirânicos substituídos

4. Synthesis of tetrahydropyrans and related heterocycles via prins cyclization; extension to aza-prins cyclization

5. (±)-cis-(6-Ethyl-tetrahydropyran-2-yl)-formic acid: a novel substance with antinociceptive properties

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