Literature DB >> 12929358

A convenient route to the furopyran core of dysiherbaine.

Okiko Miyata1, Ryuichi Iba, Jun Hashimoto, Takeaki Naito.   

Abstract

The bicyclic core, furo[3,2-b]pyran, of the dysiherbaines has been synthesized via two routes involving the imino 1,2-Wittig rearrangement of allyl furohydroximate and the asymmetric dihydroxylation of furylpropenol derivative.

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Year:  2003        PMID: 12929358     DOI: 10.1039/b212556k

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


  2 in total

1.  Synthesis of the dysiherbaine tetrahydropyran core employing a tethered aminohydroxylation reaction.

Authors:  Jamie L Cohen; A Richard Chamberlin
Journal:  Tetrahedron Lett       Date:  2007-04-02       Impact factor: 2.415

2.  Effects of alpha-Alkoxy Substitution and Conformational Constraints on 6-exo Radical Cyclizations of Hydrazones via Reversible Thiyl and Stannyl Additions.

Authors:  Gregory K Friestad; Alex K Mathies
Journal:  Tetrahedron       Date:  2007-09-17       Impact factor: 2.457

  2 in total

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