Literature DB >> 15606097

Alkynyltrifluoroborates as versatile tools in organic synthesis: a new route to spiroketals.

Jan Doubský1, Ludvík Streinz, David Saman, Jirí Zedník, Bohumír Koutek.   

Abstract

[reaction: see text] A simple and efficient two-step approach to spiroketals is described. Key steps include the preparation of functionalized hydroxyl alpha-alkynones by ring-opening reactions of lactones with lithium alkynyltrifluoroborates followed by a palladium-catalyzed hydrogenation/spirocyclization of the prespiroketal intermediate.

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Year:  2004        PMID: 15606097     DOI: 10.1021/ol047987k

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Preparation of the 5/5-spiroketal of the ritterazines.

Authors:  Douglass F Taber; Jean-Michel Joerger
Journal:  J Org Chem       Date:  2007-03-31       Impact factor: 4.354

2.  Evidence that Cerambycid Beetles Mimic Vespid Wasps in Odor as well as Appearance.

Authors:  Robert F Mitchell; Tomislav Curkovic; Judith A Mongold-Diers; Lara Neuteboom; Hans-Martin Galbrecht; Armin Tröger; Jan Bergmann; Wittko Francke; Lawrence M Hanks
Journal:  J Chem Ecol       Date:  2016-12-19       Impact factor: 2.626

  2 in total

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