✦ LIBER ✦

Synthesis of enantiomerically pure 3-amino-1,2-diols by reductive amination of racemic 2,3-dialkoxyketones

✍ Scribed by Pierre Hutin; Yves Petit; Marc Larchevêque

Book ID: 104260095
Publisher: Elsevier Science
Year: 1998
Tongue: French
Weight: 233 KB
Volume: 39
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(98)01856-5

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Synthesis of Enanti

ChemInform Abstract: Synthesis of Enantiomerically Pure 3-Amino-1,2-diols by Reductive Amination of Racemic 2,3-Dialkoxyketones.

✍ P HUTIN; Y. PETIT; M. LARCHEVEQUE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

Diastereoselective synthesis of 3-amino-

Diastereoselective synthesis of 3-amino-1,2-diols by reductive alkylation of 2,3-dialkoxynitriles

✍ Pierre Hutin; Marc Larchevêque 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 126 KB

ChemInform Abstract: Diastereoselective

ChemInform Abstract: Diastereoselective Synthesis of 3-Amino-1,2-diols by Reductive Alkylation of 2,3-Dialkoxynitriles.

✍ Pierre Hutin; Marc Larcheveque 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

ChemInform Abstract: Chemoenzymatic Synt

ChemInform Abstract: Chemoenzymatic Synthesis of Glycosylated Enantiomerically Pure 4-Pentene 1,2- and 1,3-Diol Derivatives.

✍ F. BIEN; T. ZIEGLER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Synthesis of enantiomerically pure 3-but

Synthesis of enantiomerically pure 3-butene-1,2-diol derivatives via a sharpless asymmetric epoxidation route.

✍ Constantin Neagu; Tapio Hase 📂 Article 📅 1993 🏛 Elsevier Science 🌐 French ⚖ 146 KB

3-Butene-1,2-diol: An attractive precurs

3-Butene-1,2-diol: An attractive precursor for the synthesis of enantiomerically pure organic compounds

✍ AV Rama Rao; D Subhas Bose; M.K. Gurjar; T Ravindranathan 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 535 KB

3-Butene-I,2-diol obtained by the isomerlzatlon of cls-butene-1,4-dlol has been transformed into several choral bulldmg blocks. Small and polyfunctlonal chiral bullding blocks form a backbone of research in the area of natural product chemistry. lntroductlon of new choral building blocks with a wide