Issue 4, 1994

Synthesis of oxo-2-alkenylboronates and their cyclization to 3-methylene cycloalkanols via intramolecular allylboration

Abstract

The cross-coupling reaction between halocarbonyl compounds with Knochel's (dialkoxyboryl)methylzinc reagent provided a new synthesis of oxoalk-2-enylboronates; the in situ cyclization of these boronates gave 3-methylene cyclopentanols or cycloheptanols in high yields.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 467-468

Synthesis of oxo-2-alkenylboronates and their cyclization to 3-methylene cycloalkanols via intramolecular allylboration

T. Watanabe, M. Sakai, N. Miyaura and A. Suzuki, J. Chem. Soc., Chem. Commun., 1994, 467 DOI: 10.1039/C39940000467

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