Synthesis of amino-1, 4-anhydro-d-pentitols and amino-1, 5-anhydro-d-hexitols with the arabino configuration from (R)-glycidol

S Aragonès, F Bravo, Y Dı́az, MI Matheu…

Index: Aragones, Silvia; Bravo, Fernando; Diaz, Yolanda; Matheu, Ma. Isabel; Castillon, Sergio Tetrahedron Asymmetry, 2003 , vol. 14, # 13 p. 1847 - 1856

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Citation Number: 14

Abstract

2-Amino-1, 4-anhydro-pentitol and 3-amino-1, 5-anhydro-4-deoxy-hexitol with the arabino configuration were synthesised from (R)-glycidol using a metathesis reaction as the key step. The dihydrofuran or dihydropyran products obtained after the metathesis reaction were subjected to epoxidation, epoxide opening with azide anion and finally azide reduction.

Enantioselective allyltitanations. Synthesis of optically active 1, 2-diol units: useful intermediates for the preparation of biologically active compounds

[Cossy, Janine; Bouzbouz, Samir; Caille, Jean Claude Tetrahedron Asymmetry, 1999 , vol. 10, # 20 p. 3859 - 3862]

Macrocyclic bisindolylmaleimides: synthesis by inter-and intramolecular alkylation

[Faul, Margaret M.; Winneroski, Leonard L.; Krumrich, Christine A.; Sullivan, Kevin A.; Gillig, James R.; Neel, David A.; Rito, Christopher J.; Jirousek, Michael R. Journal of Organic Chemistry, 1998 , vol. 63, # 6 p. 1961 - 1973]

Macrocyclic bisindolylmaleimides: synthesis by inter-and intramolecular alkylation

Enantioselective allyltitanations. Synthesis of optically active 1, 2-diol units: useful intermediates for the preparation of biologically active compounds

[Cossy, Janine; Bouzbouz, Samir; Caille, Jean Claude Tetrahedron Asymmetry, 1999 , vol. 10, # 20 p. 3859 - 3862]

Macrocyclic bisindolylmaleimides: synthesis by inter-and intramolecular alkylation

Synthesis of amino-1, 4-anhydro-d-pentitols and amino-1, 5-anhydro-d-hexitols with the arabino configuration from (R)-glycidol

Abstract

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