Literature DB >> 18802534

Brønsted acid catalyzed regioselective aza-Ferrier reaction: a novel synthetic method for alpha-(N-Boc-2-pyrrolidinyl) aldehydes.

Eiji Tayama1, Seijun Otoyama, Wataru Isaka.   

Abstract

The 1,4-elimination reaction of (Z)-N-Boc-2-(4-methoxy-2-alkenyloxy)pyrrolidines is shown to proceed with high (1E,3E)-stereoselectivity to afford N-Boc-2-(1,3-dienyloxy)pyrrolidines; the Brønsted acid catalyzed aza-Ferrier reaction of the N-Boc-2-(1,3-dienyloxy)pyrrolidines (3) provides alpha-(N-Boc-2-pyrrolidinyl) aldehydes in excellent yields with high alpha-regioselectivities.

Entities:  

Year:  2008        PMID: 18802534     DOI: 10.1039/b806492j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  A modular, efficient, and stereoselective synthesis of substituted piperidin-4-ols.

Authors:  Li Cui; Chaoqun Li; Liming Zhang
Journal:  Angew Chem Int Ed Engl       Date:  2010-11-22       Impact factor: 15.336

Review 2.  The Petasis-Ferrier rearrangement: developments and applications.

Authors:  Emily C Minbiole; Kevin P C Minbiole
Journal:  J Antibiot (Tokyo)       Date:  2016-01-06       Impact factor: 2.649

  2 in total

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