Literature DB >> 12398517

A stereodivergent approach to substituted 4-hydroxypiperidines.

Mandy K S Vink1, Christien A Schortinghuis, Jordy Luten, Jan H Van Maarseveen, Hans E Schoemaker, Henk Hiemstra, Floris P J T Rutjes.   

Abstract

A stereodivergent route toward both diastereomeric forms of functionalized 4-hydroxypiperidines has been successfully developed. This route involves biocatalytic generation of the enantiopure starting materials followed by functionalization via N-acyliminium ion-mediated CC-bond formation.

Entities:  

Year:  2002        PMID: 12398517     DOI: 10.1021/jo025943o

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


  3 in total

1.  Spectroscopic and X-ray crystallographic evidence for electrostatic effects in 4-substituted cyclohexanone-derived hydrazones, imines, and corresponding salts.

Authors:  David J Dibble; Joseph W Ziller; K A Woerpel
Journal:  J Org Chem       Date:  2011-09-14       Impact factor: 4.354

Review 2.  The Shono-type electroorganic oxidation of unfunctionalised amides. Carbon-carbon bond formation via electrogenerated N-acyliminium ions.

Authors:  Alan M Jones; Craig E Banks
Journal:  Beilstein J Org Chem       Date:  2014-12-18       Impact factor: 2.883

Review 3.  Rhodococcus as A Versatile Biocatalyst in Organic Synthesis.

Authors:  Hanna Busch; Peter-Leon Hagedoorn; Ulf Hanefeld
Journal:  Int J Mol Sci       Date:  2019-09-26       Impact factor: 5.923

  3 in total

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