Enantioselective total synthesis of 9S-dihydroerythronolide A seco acid
- 1 August 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 111 (16) , 6247-6256
- https://doi.org/10.1021/ja00198a041
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Acyclic stereoselection. 43. Stereoselective synthesis of the C-8 to C-15 moiety of erythronolide AThe Journal of Organic Chemistry, 1988
- Practical synthesis of diastereomerically and enantiomerically pure 2-methyl 1,3-diols from (R)-2,3,O-isopropylideneglyceraldehyde. Application to the C(1)-C(7) and C(9)-C(12) fragments of erythronolide BThe Journal of Organic Chemistry, 1987
- A chiral synthesis of 3,5,7-tri-O-benzyl-1,4,6-trideoxy-4,6-di-C-methyl-keto-l-ido-2-heptulose, a synthetic segment of the C-1–C-6 portion of erythronolide ACarbohydrate Research, 1982
- Assembly of the carbon skeletal framework of erythronolide ACanadian Journal of Chemistry, 1978
- ILOTYCIN, A NEW ANTIBIOTIC1952