Carbamate mediated 1,3-asymmetric induction. A stereoselective synthesis of acyclic 1,3-diol systems
- 31 December 1982
- journal article
- Published by Elsevier BV in Tetrahedron Letters
- Vol. 23 (50), 5307-5310
- https://doi.org/10.1016/s0040-4039(00)85825-6
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Reductive ring openings of allyl-alcohol epoxidesTetrahedron Letters, 1982
- A chiral total synthesis of compactinJournal of the American Chemical Society, 1982
- Synthesis of saccharides and related polyhydroxylated natural products. 2. Simple deoxyalditolsThe Journal of Organic Chemistry, 1982
- Stereocontrolled synthesis of D-pentitols, 2-amino-2-deoxy-D-pentitols and 2-deoxy-D-pentitols from D-glyceraldehyde acetonideJournal of the American Chemical Society, 1982
- Therapeutic effects of ML-236B in primary hypercholesterolemiaAtherosclerosis, 1980
- Hypolipidemic effects in dogs of ML-236B, a competitive inhibitor of 3-hydroxy-3-methylglutaryl coenzyme a reductaseAtherosclerosis, 1979
- ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogensis produced by Penicillium citrinum.The Journal of Antibiotics, 1976
- Polyene macrolide antibiotic amphotericin B. Crystal structure of the N-iodoacetyl derivativeJournal of the American Chemical Society, 1971