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Stereoselective Synthesis of Quaternary Center Bearing Azetines and Their β-Amino Acid Derivatives
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inferredcites →https://doi.org/10.1002/1521-3773(20011217)40:24<4591::aid-anie4591>3.0.co;2-vopenalex-snapshot
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Diastereoselective Addition of Chlorotitanium Enolate of N-Acyl Thiazolidinethione to O-Methyl Oximes: A Novel, Stereoselective Synthesis of α,β-Disubstituted β-Amino Carbonyl Compounds via Chiral Auxiliary Mediated Azetine Formation
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A Practical and Efficient Large-Scale Preparation of (4R,5S)-N-Propenoyl-1,5- dimethyl-4-phenylimidazolidin-2-one. A Simple Procedure for the Preparation of N-Acylimidazolidin-2-ones and N-Acylbornane 2,10-Sultams
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A Uniquely Accessible Route to the Diastereoselective Synthesis of Azetine Derivatives
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A NEW ANTIBIOTIC, NEGAMYCIN
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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ChemInform Abstract: Stereoselective Synthesis of Quaternary Center Bearing Azetines and Their β‐Amino Acid Derivatives.
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Alkali Carbonate Effects onN-(2-Hydroxyethyl)ureaCyclization: Application to a 2-Imidazolidinone Scale-Up
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Ring Expansions of Azirines and Azetines
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inferred← citeshttps://doi.org/10.1016/j.tet.2016.04.023openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetasy.2009.01.018openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetasy.2015.01.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/ja.2013.21openalex-snapshot
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