A formal total synthesis of (±)-pseudomonic acid A
- 1 October 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (42) , 7631-7634
- https://doi.org/10.1016/0040-4039(95)01590-e
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- A total synthesis of (.+-.)-tirandamycin BJournal of the American Chemical Society, 1991
- Enantioselective total synthesis of (-)-monic acid C via carbosulfenylation of a dihydropyranThe Journal of Organic Chemistry, 1988
- Microbial Asymmetric Catalysis—Enantioselective Reduction of Ketones [New Synthetic Methods (45)]Angewandte Chemie International Edition in English, 1984
- Synthetic application of a substituent controlled claisen rearrangement. Preparation of advanced chiral intermediates for the synthesis of pseudomonic acidsTetrahedron Letters, 1984
- Reductive cleavage of glycosidesJournal of the American Chemical Society, 1982
- The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural ProductsSynthesis, 1981
- Applications of Ionic Hydrogenation to Organic SynthesisSynthesis, 1974
- Oxidation of furans - I. synthesis of 6-hydroxy-2H-pyran-3(6H)-onesTetrahedron Letters, 1972
- Pseudomonic Acid: an Antibiotic produced by Pseudomonas fluorescensNature, 1971
- Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squaleneJournal of the American Chemical Society, 1970