Literature DB >> 15467242

A novel and concise synthesis of spirodienone alkaloids using hypervalent iodine(III) reagents.

Hiromi Hamamoto1, Yukiko Shiozaki, Kayoko Hata, Hirofumi Tohma, Yasuyuki Kita.   

Abstract

Intramolecular oxidative coupling reaction of N-protected benzyltetrahydroisoquinoline derivatives using hypervalent iodine(III) reagents was investigated. The use of remarkable combination of phenyliodine bis (trifluoroacetate) (PIFA) and heteropoly acid (HPA) in wet acetonitrile smoothly afforded morphinandienone alkaloids, while neospirinedienone alkaloids were obtained in high yield under anhydrous conditions.

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Year:  2004        PMID: 15467242     DOI: 10.1248/cpb.52.1231

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  2 in total

Review 1.  Chemistry of polyvalent iodine.

Authors:  Viktor V Zhdankin; Peter J Stang
Journal:  Chem Rev       Date:  2008-12       Impact factor: 60.622

2.  Convenient Synthesis of 6,7,12,13-Tetrahydro-5H-Cyclohepta[2,1-b:3,4-b']diindole Derivatives Mediated by Hypervalent Iodine (III) Reagent.

Authors:  Lei Peng; Xiaofei Zhang; Chunhao Yang
Journal:  Molecules       Date:  2019-03-08       Impact factor: 4.411

  2 in total

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