Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1978, 43, 1720-1722
https://doi.org/10.1135/cccc19781720

Stereoselective reduction of 1,6-anhydro-3,4-dideoxy-β-D-glycero-hex-3-enopyranos-2-ulose (levoglucosenone) and of its 3,4-dihydro derivative with complex hydrides

Jaroslav Pecka and Miloslav Černý

Crossref Cited-by Linking

  • Tagirov A. R., Biktagirov I. M., Galimova Yu. S., Faizullina L. Kh., Salikhov Sh. M., Valeev F. A.: Opening of the 1,6-anhydro bridge with selective reduction of the acetal moiety in levoglucosenone and its derivatives. Russ J Org Chem 2015, 51, 569. <https://doi.org/10.1134/S1070428015040181>
  • Miftakhov Mansur S, Valeev Farid A, Gaisina Irina N: Levoglucosenone: the properties, reactions, and use in fine organic synthesis. Russ. Chem. Rev. 1994, 63, 869. <https://doi.org/10.1070/RC1994v063n10ABEH000123>
  • Gelas-Mialhe Yvonne, Gelas Jacques: New branched-chain and aminodeoxy sugars from 1,6-anhydro-3,4-dideoxy-β-d-glycero-hex-3-enopyranos-2-ulose (levoglucosenone). Carbohydrate Research 1990, 199, 243. <https://doi.org/10.1016/0008-6215(90)84267-X>
  • Toromanoff E.: Dynamic stereochemistry of the 5-, 6- and 7-membered rings using the torsion angle notation. Tetrahedron 1980, 36, 2809. <https://doi.org/10.1016/0040-4020(80)88015-X>
  • PECKA J., CERNY M.: ChemInform Abstract: STEREOSELECTIVE REDUCTION OF 1,6-ANHYDRO-3,4-DIDEOXY-β-D-GLYCERO-HEX-3-ENOPYRANOS-2-ULOSE (LEVOGLUCOSENONE) AND OF ITS 3,4-DIHYDRO DERIVATIVE WITH COMPLEX HYDRIDES. Chemischer Informationsdienst 1978, 9. <https://doi.org/10.1002/chin.197847102>