Densely Functionalized 2-Methylideneazetidines from Nitrodienic Building Blocks

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Densely Functionalized 2-Methylideneazetidines from Nitrodienic Building Blocks

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im Januar 2018 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в січні 2018

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Densely Functionalized 2-Methylideneazetidines from Nitrodienic Building Blocks

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Densely Functionalized 2-Methylideneazetidines from Nitrodienic Building Blocks

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Densely Functionalized 2-Methylideneazetidines from Nitrodienic Building Blocks

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Densely Functionalized 2-Methylideneazetidines from Nitrodienic Building Blocks

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Densely Functionalized 2-Methylideneazetidines from Nitrodienic Building Blocks

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Densely Functionalized 2-Methylideneazetidines from Nitrodienic Building Blocks

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P1476

Densely Functionalized 2-Methylideneazetidines from Nitrodienic Building Blocks

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P2093

Cinzia Tavani

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Gianluca Giorgi

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Giovanni Petrillo

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Lara Bianchi

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Massimo Maccagno

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P2860

A short history of SHELX

Rules for ring closure

Azetidine-2-carboxylic acid in garden beets (Beta vulgaris).

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

Crystal structure refinement with SHELXL.

Novel syntheses of azetidines and azetidinones.

Recent advances in the chemistry of metallated azetidines.

Synthesis of a Bicyclic Azetidine with In Vivo Antimalarial Activity Enabled by Stereospecific, Directed C(sp3)-H Arylation.

Ring-opening/ring-closing protocols from nitrothiophenes: six-membered versus unusual eight-membered sulfur heterocycles through Michael-type addition on nitrobutadienes.

Access to ring-fused homo- and heteroaromatic derivatives via an initial ring-opening of 3-nitro-4-(phenylsulfonyl)thiophene.

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126-136

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P31

scholarly article

P356

10.1002/EJOC.201701467

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P433

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P478

2018

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P577

2018-01-10T00:00:00Z

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