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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 37, 2007 - Issue 22
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Original Articles

Practical Preparation of β‐Amino‐α‐Hydroxy Diesters: Key Intermediates for 1,4‐Oxazin‐2‐Ones

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Pages 3989-4004 | Received 12 Jun 2006, Published online: 19 Nov 2007

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Read on this site (4)

Soumaya Slama, Brahim Ould Elemine & Rafâa Besbes. (2013) Convenient Synthesis of 1,2-Diamines from β-Chloro Amines: Precursors of New Substituted Piperazin-2-ones. Synthetic Communications 43:17, pages 2286-2293.
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Amani Kaabi & Rafâa Besbes. (2013) Amino Phosphate Monoesters: A Convenient Source of 2-Alkylamino-3-methoxy-3-phenylpropionates via Aziridinium Ions. Synthetic Communications 43:11, pages 1587-1593.
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Amani Kaabi, Brahim Ould Elemine & Rafâa Besbes. (2011) A One-Pot Synthesis of trans-N-Alkylaziridine-2-carboxylates from Amino Alcohol Esters. Synthetic Communications 41:10, pages 1472-1480.
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Brahim Ould Elemine, Rafâa Besbes & Mohamed Rached Ennigrou. (2009) Straightforward Synthesis of 1,2-Amino Phosphate Diesters and Application to the Synthesis of Novel 1,2-Amino Ether Diesters. Synthetic Communications 40:1, pages 64-73.
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Articles from other publishers (4)

Mohamed Ali Tabarki & Rafâa Besbes. (2014) Regioselective ring opening of β-phenylglycidate and aziridine-2-carboxylates with N-alkylhydroxylamines: synthesis of isoxazolidinones. Tetrahedron 70:5, pages 1060-1064.
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Brahim Ould Elemine, Mohamed Rached Ennigrou & Rafâa Besbes. (2011) Stereoselective synthesis of functional dehydrophenylalanine derivatives from novel β‐chloroamino esters. Heteroatom Chemistry 23:1, pages 91-98.
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Christine Philippe, Thierry Milcent, Benoit Crousse & Danièle Bonnet-Delpon. (2009) Non Lewis acid catalysed epoxide ring opening with amino acid esters. Organic & Biomolecular Chemistry 7:10, pages 2026.
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Brahim Ould Elemine, Rafaa Besbes & Mohamed Rached Ennigrou. (2008) ChemInform Abstract: Practical Preparation of β‐Amino‐α‐hydroxy Diesters: Key Intermediates for 1,4‐Oxazin‐2‐ones.. ChemInform 39:17.
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