SYNTHESIS OF 8,9-LEUKOTRIENE-C3 AND 8,9-LEUKOTRIENE-D3

[1] LEUKOTRIENES - A MAJOR STEP IN THE UNDERSTANDING OF IMMEDIATE HYPERSENSITIVITY REACTIONS [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1981, 24 (02) : 121 - 126

[2] TOTAL SYNTHESIS OF SLOW REACTING SUBSTANCES (SRS) - LEUKOTRIENE C-2 (11-TRANS-LEUKOTRIENE-C)-(3) AND LEUKOTRIENE-D-(4) [J]. TETRAHEDRON LETTERS, 1980, 21 (33) : 3143 - 3146

[3] STEREOSPECIFIC TOTAL SYNTHESIS OF A SLOW REACTING SUBSTANCE OF ANAPHYLAXIS, LEUKOTRIENE C-1 [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (04) : 1436 - 1439

[4] DAHLEN S-E, 1983, European Journal of Pharmacology, V86, P207

[5] HAMMARSTROM S, 1981, J BIOL CHEM, V256, P7712

[6] THE 1ST PRACTICAL METHOD FOR ASYMMETRIC EPOXIDATION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (18) : 5974 - 5976

[7] LEUKOTRIENE-C - SLOW-REACTING SUBSTANCE FROM MURINE MASTOCYTOMA-CELLS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (09) : 4275 - 4279

[8] MICROBIOLOGICALLY ACTIVE 4-THIAZOLIDONES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (01) : 109 - 114

[9] ASYMMETRIC EPOXIDATION PROVIDES SHORTEST ROUTES TO 4 CHIRAL EPOXY ALCOHOLS WHICH ARE KEY INTERMEDIATES IN SYNTHESES OF METHYMYCIN, ERYTHROMYCIN, LEUKOTRIENE C-1, AND DISPARLURE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (02) : 464 - 465

[1] LEUKOTRIENES - A MAJOR STEP IN THE UNDERSTANDING OF IMMEDIATE HYPERSENSITIVITY REACTIONS [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1981, 24 (02) : 121 - 126

[2] TOTAL SYNTHESIS OF SLOW REACTING SUBSTANCES (SRS) - LEUKOTRIENE C-2 (11-TRANS-LEUKOTRIENE-C)-(3) AND LEUKOTRIENE-D-(4) [J]. TETRAHEDRON LETTERS, 1980, 21 (33) : 3143 - 3146

[3] STEREOSPECIFIC TOTAL SYNTHESIS OF A SLOW REACTING SUBSTANCE OF ANAPHYLAXIS, LEUKOTRIENE C-1 [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (04) : 1436 - 1439

[4] DAHLEN S-E, 1983, European Journal of Pharmacology, V86, P207

[5] HAMMARSTROM S, 1981, J BIOL CHEM, V256, P7712

[6] THE 1ST PRACTICAL METHOD FOR ASYMMETRIC EPOXIDATION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1980, 102 (18) : 5974 - 5976

[7] LEUKOTRIENE-C - SLOW-REACTING SUBSTANCE FROM MURINE MASTOCYTOMA-CELLS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (09) : 4275 - 4279

[8] MICROBIOLOGICALLY ACTIVE 4-THIAZOLIDONES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (01) : 109 - 114

[9] ASYMMETRIC EPOXIDATION PROVIDES SHORTEST ROUTES TO 4 CHIRAL EPOXY ALCOHOLS WHICH ARE KEY INTERMEDIATES IN SYNTHESES OF METHYMYCIN, ERYTHROMYCIN, LEUKOTRIENE C-1, AND DISPARLURE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (02) : 464 - 465