1,6-Anhydroglucose in organic synthesis; preparation of fragments suitable for natural product synthesis
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (34), 4111-4114
- https://doi.org/10.1016/s0040-4039(00)89306-5
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- A stereoselective synthesis of 1,3-diol derivatives and application to the ansa bridge of rifamycin SJournal of the American Chemical Society, 1983
- Total synthesis of the structurally unique ionophore antibiotic X–14547 AJournal of the Chemical Society, Chemical Communications, 1983
- Asymmetric total synthesis of erythromcin. 1. Synthesis of an erythronolide A secoacid derivative via asymmetric inductionJournal of the American Chemical Society, 1981
- Total synthesis of rifamycins. 2. Total synthesis of racemic rifamycin SJournal of the American Chemical Society, 1980
- Total synthesis of rifamycins. 1. Stereocontrolled synthesis of the aliphatic building blockJournal of the American Chemical Society, 1980
- A simple, stereocontrolled synthesis of a thromboxane B2 synthonJournal of the Chemical Society, Chemical Communications, 1980
- 1,6-Anhydro Derivatives of AldohexosesPublished by Elsevier ,1977
- X-ray structure of tirandamycic acid p-bromophenacyl ester. Complete stereochemical assignments of tirandamycin and streptolydiginJournal of the American Chemical Society, 1973
- Structure of monensic acid, a new biologically active compoundJournal of the American Chemical Society, 1967
- Preparation of 2- and 4-Substituted D-Glucose Derivatives from 1,6-Anhydro-β-D- glucopyranose1The Journal of Organic Chemistry, 1965