5 (S), 6(R)-5. 7-dibenzoyloxy-6-hydroxyheptanoate ester: improved synthesis of a leukotriene intermediate
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (37) , 3657-3658
- https://doi.org/10.1016/s0040-4039(01)81985-7
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Synthesis of leukotrienes - new synthesis of natural leukotriene A4Tetrahedron Letters, 1981
- Chirally directed synthesis of (-)-methyl 5(S), 6(S)-oxido-7-hydroxyheptanoate, a key intermediate for the total synthesis of leukotrienes A, C, D and EJournal of the American Chemical Society, 1981
- Asymmetric epoxidation provides shortest routes to four chiral epoxy alcohols which are key intermediates in syntheses of methymycin, erythromycin, leukotriene C-1, and disparlureJournal of the American Chemical Society, 1981
- The synthesis of a leukotriene with SRS-like activityTetrahedron Letters, 1980
- Synthesis, separation and N.M.R. spectra of three double bond isomers of leukotriene a methyl esterTetrahedron Letters, 1980
- Synthesis of optically active leukotriene (SRS-A) intermediatesTetrahedron Letters, 1980
- Total synthesis of (5S,6R,7E,9E,11Z,14Z)-5-hydroxy-6-[(2R)-2-amino-2-(carboxyethyl)thio]-7,9,11,14-eicosatetraenoic acid, a potent SRS-AJournal of the American Chemical Society, 1980
- Stereospecific total synthesis of a "slow reacting substance" of anaphylaxis, leukotriene C-1Journal of the American Chemical Society, 1980
- Convergent synthesis of leukotriene a methyl esterTetrahedron Letters, 1980
- Branched-chain N-sugar nucleosides : Part IV. Nucleosides of 3-C-branched-chain, 3-C-(cyanomethyl)- and 3-C-(2-aminoethyl)-2,3-dideoxy-D-threo-pentoseCarbohydrate Research, 1974