Literature DB >> 21235246

Synthesis of novel angular spirocyclic azetidines.

Carine Guérot1, Boris H Tchitchanov, Henner Knust, Erick M Carreira.   

Abstract

The syntheses of a variety of novel angular azaspiro[3.3]heptanes are reported. gem-Difluoro and gem-dimethyl variants of the angular 1,6-diazaspiro[3.3]heptane module were prepared in high yields using efficient sequences. Additionally, a practical one-pot synthesis of 5-oxo-2-azaspiro[3.3]heptanes and subsequent conversions into functionalized derivatives are described. The methods reported are amenable to the synthesis of these building blocks for drug discovery as members of a library or individually on a preparative scale.

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Year:  2011        PMID: 21235246     DOI: 10.1021/ol103050c

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Synthesis and profiling of a diverse collection of azetidine-based scaffolds for the development of CNS-focused lead-like libraries.

Authors:  Jason T Lowe; Maurice D Lee; Lakshmi B Akella; Emeline Davoine; Etienne J Donckele; Landon Durak; Jeremy R Duvall; Baudouin Gerard; Edward B Holson; Adrien Joliton; Sarathy Kesavan; Berenice C Lemercier; Haibo Liu; Jean-Charles Marié; Carol A Mulrooney; Giovanni Muncipinto; Morgan Welzel-O'Shea; Laura M Panko; Ann Rowley; Byung-Chul Suh; Meryl Thomas; Florence F Wagner; Jingqiang Wei; Michael A Foley; Lisa A Marcaurelle
Journal:  J Org Chem       Date:  2012-08-10       Impact factor: 4.354

2.  Accelerating fragment-based library generation by coupling high-performance photoreactors with benchtop analysis.

Authors:  Quentin Lefebvre; Christophe Salomé; Thomas C Fessard
Journal:  Beilstein J Org Chem       Date:  2020-05-12       Impact factor: 2.883

3.  Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation of Thietane 1,1-Dioxides.

Authors:  Gillian Laidlaw; Vilius Franckevičius
Journal:  Org Lett       Date:  2021-12-16       Impact factor: 6.005

  3 in total

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