Year |
Citation |
Score |
1985 |
Marfat A, Corey EJ. Synthesis and structure elucidation of leukotrienes. Advances in Prostaglandin, Thromboxane, and Leukotriene Research. 14: 155-228. PMID 2992244 |
0.523 |
|
1985 |
COREY EJ, CLARK DA, MARFAT A. ChemInform Abstract: STRUCTURE ELUCIDATION AND TOTAL SYNTHESIS OF THE LEUKOTRIENES Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198510383 |
0.592 |
|
1983 |
BAL SA, MARFAT A, HELQUIST P. ChemInform Abstract: CYCLOPENTENE AND CYCLOHEXENE ANNULATION VIA COPPER-CATALYZED CONJUGATE ADDITION OF ACETAL-CONTAINING GRIGNARD REAGENTS Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198322121 |
0.672 |
|
1982 |
Lewis RA, Mencia-Huerta JM, Soberman RJ, Hoover D, Marfat A, Corey EJ, Austen KF. Radioimmunoassay for leukotriene B4. Proceedings of the National Academy of Sciences of the United States of America. 79: 7904-8. PMID 6296855 DOI: 10.1073/Pnas.79.24.7904 |
0.551 |
|
1982 |
Showell HJ, Otterness IG, Marfat A, Corey EJ. Inhibition of leukotriene B4-induced neutrophil degranulation by leukotriene B4-dimethylamide. Biochemical and Biophysical Research Communications. 106: 741-7. PMID 6288032 DOI: 10.1016/0006-291X(82)91773-9 |
0.516 |
|
1982 |
Bal SA, Marfat A, Helquist P. Cyclopentene and cyclohexene annulation via copper-catalyzed conjugate addition of acetal-containing Grignard reagents The Journal of Organic Chemistry. 47: 5045-5050. DOI: 10.1021/Jo00147A001 |
0.685 |
|
1981 |
Levine L, Morgan RA, Lewis RA, Austen KF, Clark DA, Marfat A, Corey EJ. Radioimmunoassay of the leukotrienes of slow reacting substance of anaphylaxis. Proceedings of the National Academy of Sciences of the United States of America. 78: 7692-6. PMID 6950409 DOI: 10.1073/Pnas.78.12.7692 |
0.547 |
|
1981 |
Drazen JM, Lewis RA, Austen KF, Toda M, Brion F, Marfat A, Corey EJ. Contractile activities of structural analogs of leukotrienes C and D: necessity of a hydrophobic region. Proceedings of the National Academy of Sciences of the United States of America. 78: 3195-8. PMID 6942424 DOI: 10.1073/Pnas.78.5.3195 |
0.65 |
|
1981 |
Lewis RA, Drazen JM, Austen KF, Toda M, Brion F, Marfat A, Corey EJ. Contractile activities of structural analogs of leukotrienes C and D: role of the polar substituents. Proceedings of the National Academy of Sciences of the United States of America. 78: 4579-83. PMID 6270684 DOI: 10.1073/Pnas.78.7.4579 |
0.648 |
|
1981 |
Corey EJ, Marfat A, Hoover DJ. Stereospecific total synthesis of 12-(r)- and 12- (s)-forms of 6-trans leukotriene B Tetrahedron Letters. 22: 1587-1590. DOI: 10.1016/S0040-4039(01)90384-3 |
0.6 |
|
1981 |
Corey EJ, Marfat A, Munroe J, Kim KS, Hopkins PB, Brion F. A Stereocontrolled and effective synthesis of leukotriene B (1). Tetrahedron Letters. 22: 1077-1080. DOI: 10.1016/S0040-4039(01)90241-2 |
0.751 |
|
1981 |
Corey EJ, Marfat A, Laguzza BC. Total synthesis of 5S, 12S-dihydroxy-6,10-E,8,14-Z-eicosatetraenoic acid (5S,12S-di-HETE) (2), a new human metabolite of arachidonic acid Tetrahedron Letters. 22: 3339-3342. DOI: 10.1016/S0040-4039(01)81899-2 |
0.571 |
|
1981 |
COREY EJ, HOPKINS PB, MUNROE JE, MARFAT A, HASHIMOTO S. ChemInform Abstract: TOTAL SYNTHESIS OF 6-TRANS,10-CIS AND (.+-.)-6-TRANS,8-CIS ISOMERS OF LEUKOTRIENE B Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198114329 |
0.697 |
|
1980 |
Corey EJ, Niwa H, Falck JR, Mioskowski C, Arai Y, Marfat A. Recent studies on the chemical synthesis of eicosanoids. Advances in Prostaglandin and Thromboxane Research. 6: 19-25. PMID 7386258 |
0.527 |
|
1980 |
Drazen JM, Austen KF, Lewis RA, Clark DA, Goto G, Marfat A, Corey EJ. Comparative airway and vascular activities of leukotrienes C-1 and D in vivo and in vitro. Proceedings of the National Academy of Sciences of the United States of America. 77: 4354-8. PMID 6933488 DOI: 10.1073/Pnas.77.7.4354 |
0.489 |
|
1980 |
Clark DA, Goto G, Marfat A, Corey EJ, Hammarström S, Samuelsson B. 11-Trans leukotriene C: a naturally occurring slow reacting substance. Biochemical and Biophysical Research Communications. 94: 1133-9. PMID 6772184 DOI: 10.1016/0006-291X(80)90537-9 |
0.674 |
|
1980 |
Rådmark O, Malmsten C, Samuelsson B, Goto G, Marfat A, Corey EJ. Leukotriene A. Isolation from human polymorphonuclear leukocytes. The Journal of Biological Chemistry. 255: 11828-31. PMID 6254983 |
0.495 |
|
1980 |
Rådmark O, Malmsten C, Samuelsson B, Clark DA, Goto G, Marfat A, Corey EJ. Leukotriene A: stereochemistry and enzymatic conversion to leukotriene B. Biochemical and Biophysical Research Communications. 92: 954-61. PMID 6244821 DOI: 10.1016/0006-291X(80)90795-0 |
0.667 |
|
1980 |
Lewis RA, Austen KF, Drazen JM, Clark DA, Marfat A, Corey EJ. Slow reacting substances of anaphylaxis: identification of leukotrienes C-1 and D from human and rat sources. Proceedings of the National Academy of Sciences of the United States of America. 77: 3710-4. PMID 6106193 DOI: 10.1073/Pnas.77.6.3710 |
0.524 |
|
1980 |
Hammarström S, Samuelsson B, Clark DA, Goto G, Marfat A, Mioskowski C, Corey EJ. Stereochemistry of leukotriene C-1. Biochemical and Biophysical Research Communications. 92: 946-53. PMID 6102463 DOI: 10.1016/0006-291X(80)90794-9 |
0.665 |
|
1980 |
Corey E, Hopkins P, Munroe J, Marfat A, Hashimoto S. Total Synthesis of 6-Trans, 10-cis and (plus or minus) -6-Trans,8-cis Isomers of Leukotriene B Journal of the American Chemical Society. 102: 7986-7987. DOI: 10.1021/Ja00547A600 |
0.692 |
|
1980 |
Corey EJ, Marfat A, Goto G, Brion F. Leukotriene B. Total synthesis and assignment of stereochemistry Journal of the American Chemical Society. 102: 7984-7985. DOI: 10.1021/Ja00547A051 |
0.692 |
|
1980 |
Corey EJ, Goto G, Marfat A. Simple synthesis of the 11,12-oxido and 14,15-oxido analogs of leukotriene A and the corresponding conjugates with glutathione and cysteinylglycine, analogs of leukotrienes C and D Journal of the American Chemical Society. 102: 6607-6608. DOI: 10.1021/Ja00541A060 |
0.597 |
|
1980 |
Corey E, Clark D, Goto G, Marfat A, Mioskowski C, Samuelsson B, Hammarstrom S. Additions and Corrections - Stereospecific Total Synthesis of a "Slow Reacting Substance" of Anaphylaxis Leukotriene C-1 Journal of the American Chemical Society. 102: 3663-3663. DOI: 10.1021/Ja00530A611 |
0.69 |
|
1980 |
Corey EJ, Clark DA, Goto G, Marfat A, Mioskowski C, Samuelsson B, Hammarstroem S. Stereospecific total synthesis of a "slow reacting substance" of anaphylaxis, leukotriene C-1 Journal of the American Chemical Society. 102: 1436-1439. DOI: 10.1021/Ja00524A045 |
0.688 |
|
1980 |
Corey EJ, Marfat A, Falck JR, Albright JO. Controlled chemical synthesis of the enzymatically produced eicosanoids 11-, 12-, and 15-HETE from arachidonic acid and conversion into the corresponding hydroperoxides(HPETE) [13] Journal of the American Chemical Society. 102: 1433-1435. DOI: 10.1021/Ja00524A043 |
0.571 |
|
1980 |
Corey EJ, Clark DA, Marfat A, Goto G. Total synthesis of slow reacting substances (SRS). "Leukotriene C-2" (11-trans-leukotriene C) (3) and leukotriene D (4) Tetrahedron Letters. 21: 3143-3146. DOI: 10.1016/S0040-4039(00)77430-2 |
0.586 |
|
1980 |
COREY EJ, CLARK DA, MARFAT A, GOTO G. ChemInform Abstract: TOTAL SYNTHESIS OF SLOW REACTING SUBSTANCES (SRS). “LEUKOTRIENE C-2” (11-TRANS-LEUKOTRIENE C) AND LEUKOTRIENE D Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198047297 |
0.302 |
|
1980 |
COREY EJ, CLARK DA, GOTO G, MARFAT A, MIOSKOWSKI C, SAMUELSSON B, HAMMARSTROEM S. ChemInform Abstract: STEREOSPECIFIC TOTAL SYNTHESIS OF A “SLOW REACTING SUBSTANCE” OF ANAPHYLAXIS, LEUKOTRIENE C-1 Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198021155 |
0.569 |
|
1980 |
Corey EJ, Marfat A, Falck JR, Albright JO. Controlled Chemical Synthesis Of The Enzymically Produced Eicosanoids 11-, 12-, And 15-Hete From Arachidonic Acid And Conversion Into The Corresponding Hydroperoxides (Hpete) Cheminform. 11. DOI: 10.1002/Chin.198021153 |
0.552 |
|
1980 |
MARFAT A, MCGUIRK PR, HELQUIST P. ChemInform Abstract: HIGHLY STEREOSELECTIVE SYNTHESIS OF TRISUBSTITUTED OLEFINS VIA ADDITION OF ALKYLCOPPER COMPLEXES TO ACETYLENES Chemischer Informationsdienst. 11. DOI: 10.1002/chin.198018136 |
0.707 |
|
1980 |
Corey EJ, Marfat A, Goto G. Simple synthesis of the 11,12-oxido and 14,15-oxido analogues of leukotriene A and the corresponding conjugates with glutathione and cysteinylglycine, analogues of leukotrienes C and D [34] Journal of the American Chemical Society. 102: 6607-6608. |
0.318 |
|
1980 |
Corey EJ, Clark DA, Goto G, Marfat A, Mioskowski C, Samuelsson B, Hammarström S. Stereospecific total synthesis of a "slow reacting substance" of anaphylaxis, leukotriene C-1 [15] Journal of the American Chemical Society. 102: 1436-1439. |
0.334 |
|
1980 |
Corey EJ, Hopkins PB, Munroe JE, Marfat A, Hashimoto SI. Total synthesis of 6-trans,10-cis and (±)-6-trans,8-cis isomers of leukotriene B [37] Journal of the American Chemical Society. 102: 7986-7987. |
0.58 |
|
1980 |
Corey EJ, Marfat A, Goto G, Brion F. Leukotriene B. Total synthesis and assignment of stereochemistry [36] Journal of the American Chemical Society. 102: 7984-7985. |
0.575 |
|
1979 |
Marfat A, McGuirk PR, Helquist P. Highly stereoselective synthesis of trisubstituted olefins via addition of alkylcopper complexes to acetylenes The Journal of Organic Chemistry. 44: 3888-3901. DOI: 10.1021/Jo01336A029 |
0.718 |
|
1979 |
Marfat A, McGuirk PR, Helquist P. Iterative construction of trisubstituted olefin units. Short, stereoselective synthesis of the codling moth constituent, (2Z,6Z)-7-methyl-3-propyl-2,6-decadien-1-ol The Journal of Organic Chemistry. 44: 1345-1347. DOI: 10.1021/Jo01322A034 |
0.663 |
|
1979 |
Brandt S, Marfat A, Helquist P. A short, efficient, synthetic pathway to the 6,7,8,9-tetrahydro-5h-dibenz[d,f]azonine system Tetrahedron Letters. 20: 2193-2194. DOI: 10.1016/S0040-4039(01)93673-1 |
0.596 |
|
1979 |
BRANDT S, MARFAT A, HELQUIST P. ChemInform Abstract: A SHORT, EFFICIENT, SYNTHETIC PATH TO THE 6,7,8,9-TETRAHYDRO-5H-DIBENZ(D,F)>AZONINE SYSTEM Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197939188 |
0.607 |
|
1979 |
MARFAT A, HELQUIST P. ChemInform Abstract: COPPER-CATALYZED CONJUGATE ADDITION OF AN ACETAL-CONTAINING GRIGNARD REAGENT. A METHOD FOR CYCLOPENTENE ANNULATION Chemischer Informationsdienst. 10. DOI: 10.1002/chin.197909141 |
0.663 |
|
1979 |
Marfat A, McGuirk PR, Helquist P. Highly stereoselective synthesis of trisubstituted olefins via addition of alkylcopper complexes to acetylenes Journal of Organic Chemistry. 44: 3888-3901. |
0.362 |
|
1978 |
Marfat A, Helquist P. Copper-catalyzed conjugate addition of an acetal-containing grignard reagent. A method for cyclopentene annulation. Tetrahedron Letters. 19: 4217-4220. DOI: 10.1016/S0040-4039(01)95185-8 |
0.654 |
|
1978 |
McGuirk PR, Marfat A, Helquist P. Determination of the configurations of trisubstituted olefins obtained from addition of alkylcopper complexes to acetylenes. Use of a lanthanide nmr shift reagent Tetrahedron Letters. 19: 2973-2976. DOI: 10.1016/S0040-4039(01)94915-9 |
0.647 |
|
1978 |
McGuirk PR, Marfat A, Helquist P. Stereoselective synthesis of homoallylic alcohols containingtrisubstituted olefinic double bonds Tetrahedron Letters. 19: 2465-2468. DOI: 10.1016/S0040-4039(01)94801-4 |
0.626 |
|
1978 |
Marfat A, McGuirk PR, Helquist P. Addition of a methylcopper complex to acetylenes. Synthesis of trisubstituted olefins Tetrahedron Letters. 19: 1363-1366. DOI: 10.1016/S0040-4039(01)94546-0 |
0.692 |
|
1978 |
MCGUIRK PR, MARFAT A, HELQUIST P. ChemInform Abstract: DETERMINATION OF THE CONFIGURATIONS OF TRISUBSTITUTED OLEFINS OBTAINED FROM ADDITION OF ALKYLCOPPER COMPLEXES TO ACETYLENES. USE OF A LANTHANIDE NMR SHIFT REAGENT Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197847156 |
0.656 |
|
1978 |
MCGUIRK PR, MARFAT A, HELQUIST P. ChemInform Abstract: STEREOSELECTIVE SYNTHESIS OF HOMOALLYLIC ALCOHOLS CONTAINING TRISUBSTITUTED OLEFINIC DOUBLE BONDS Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197842094 |
0.64 |
|
1978 |
MARFAT A, MCGUIRK PR, HELQUIST P. ChemInform Abstract: ADDITION OF A METHYLCOPPER COMPLEX TO ACETYLENES. SYNTHESIS OF TRISUBSTITUTED OLEFINS Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197828124 |
0.701 |
|
1977 |
Marfat A, McGuirk PR, Kramer R, Helquist P. Conjugate addition of vinylcopper complexes derived from addition of alkylcopper complexes to acetylenes. A stereospecific synthesis of trisubstituted olefins Journal of the American Chemical Society. 99: 253-255. DOI: 10.1021/Ja00443A050 |
0.695 |
|
1977 |
Marfat A, McGuirk PR, Kramer R, Helquist P. Conjugate addition of vinylcopper complexes derived from addition of alkylcopper complexes to acetylenes. A stereospecific synthesis of trisubstituted olefins [10] Journal of the American Chemical Society. 99: 253-255. |
0.304 |
|
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