Literature DB >> 22651243

Allenylphosphonates/allenylphosphine oxides as intermediates/precursors for intramolecular cyclization leading to phosphorus-based indenes, indenones, benzofurans, and isochromenes.

K V Sajna1, K C Kumara Swamy.   

Abstract

Utilizing internally available functional groups, a simple protocol for the efficient synthesis of phosphorus-based indenes, indenones, benzofurans, and isochromenes via intramolecular cyclization of allene intermediates/precursors is generated; the latter intermediates/precursors are conveniently obtained through aldehyde-, alkylidene-, and hydroxyl-functionalized propargyl alcohols and P(III)-Cl precursors. The structures of key products have been unequivocally confirmed by X-ray crystallography.

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Year:  2012        PMID: 22651243     DOI: 10.1021/jo300705f

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Synthesis of γ-hydroxypropyl P-chirogenic (±)-phosphorus oxide derivatives by regioselective ring-opening of oxaphospholane 2-oxide precursors.

Authors:  Iris Binyamin; Shoval Meidan-Shani; Nissan Ashkenazi
Journal:  Beilstein J Org Chem       Date:  2015-07-30       Impact factor: 2.883

2.  Allenylphosphine oxides as simple scaffolds for phosphinoylindoles and phosphinoylisocoumarins.

Authors:  G Gangadhararao; Ramesh Kotikalapudi; M Nagarjuna Reddy; K C Kumara Swamy
Journal:  Beilstein J Org Chem       Date:  2014-05-02       Impact factor: 2.883

  2 in total

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