Zobrazeno 1 - 10
of 822
pro vyhledávání: '"WC Taylor"'
Autor:
Schindler, Christian J. A.1 (AUTHOR), Wittenberg, Ian2 (AUTHOR), Damm, Oliver3 (AUTHOR), Kramer, Rolf3 (AUTHOR), Mikolajczyk, Rafael2 (AUTHOR), Schönfelder, Tonio1,4 (AUTHOR) tonio.schoenfelder@wig2.de
Publikováno v:
Infectious Diseases & Therapy. Nov2024, Vol. 13 Issue 11, p2333-2350. 18p.
Autor:
Ueamsaranworakul, Thosapol1 (AUTHOR), Niamjumnong, Ratcharin1 (AUTHOR), Kornthatchapong, Kumpol1 (AUTHOR), Srivilaithon, Winchana1 (AUTHOR) winchanas@gmail.com
Publikováno v:
Journal of Emergencies, Trauma & Shock. Oct-Dec2024, Vol. 17 Issue 4, p212-220. 9p.
Autor:
Rachmat, Agus1 (AUTHOR), Kelly, Gerard C2 (AUTHOR), Tran, Long Khanh2 (AUTHOR), Christy, Nathaniel3 (AUTHOR), Supaprom, Chonthida1 (AUTHOR), Heang, Vireak1 (AUTHOR), Dul, Sokha1 (AUTHOR), Garcia-Rivera, Jose A4 (AUTHOR), Prom, Satharath5 (AUTHOR), Sopheab, Heng6 (AUTHOR), Brooks, John S4 (AUTHOR), Sutherland, Ian J4 (AUTHOR), Corson, Karen S3,4 (AUTHOR), Letizia, Andrew G3 (AUTHOR) Andrew.g.letizia.mil@health.mil
Publikováno v:
Open Forum Infectious Diseases. Mar2024, Vol. 11 Issue 3, p1-9. 9p.
Publikováno v:
Australian Journal of Chemistry. 45:925
The synthesis of (2RS,3SR)-4-(4-hydroxy-3,5-dimethoxyphenyl)-2,3-dimethyl-1-(3,4,5-trimethoxypheny1)butan-1-one (9) is described. Monophenolic oxidative coupling of (9) did not give any useful result. Oxidation of the derived acetoxy compound (18) by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db8d5c7f905857edb2d4a1e8fbe3b378
https://doi.org/10.1071/ch9920925
https://doi.org/10.1071/ch9920925
Publikováno v:
Australian Journal of Chemistry. 45:935
Intramolecular non- phenolic coupling of (2RS,3SR)-1,4-bis(4-benzyloxy-3,5-dimethoxyphenyl)-2,3-dimethylbutan-1-one (6) failed. Oxidation of the derived butane(9) gave the aryltetralin (14) in low yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9af1779099e4868d91ef1f0500371df6
https://doi.org/10.1071/ch9920935
https://doi.org/10.1071/ch9920935
Autor:
Lerner, Gabriel B.1 gabriel.lerner@yale.edu, Reynolds, Meredith A.2, Setty, Suman3, Deeb, Reem4, Rastogi, Prerna5, Moeckel, Gilbert1, Sanchez, Harold1, Henriksen, Kammi J.2, Chang, Anthony2
Publikováno v:
Archives of Pathology & Laboratory Medicine. Jan2024, Vol. 148 Issue 1, p74-77. 4p.
Publikováno v:
Australian Journal of Chemistry. 44:1335
The C- methylation of 3-methyl-1,4-bis(3,4,5-trimethoxyphenyl)butan-1-one (9) gave in a ratio of 4:1 the diastereoisomers, (2RS,3SR)- and (2RS,3RS)-2,3-dimethyl-1,4-bis(3,4,5-trimethoxyphenyl) butan-1-one, (7) and (8) respectively. The stereochemistr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cd924f53833e384aee0b48921c78346
https://doi.org/10.1071/ch9911335
https://doi.org/10.1071/ch9911335
Publikováno v:
Australian Journal of Chemistry. 44:1307
The synthesis of (2RS,3SR)-1-(3,5-dihydroxy-4-methoxyphenyl)-(4-hydroxy-3,5-dimethoxy-phenyl)-2,3-dimethylbutan-1-one (26) is described. Diphenolic oxidative coupling of (26) did not produce a eupodienone -type product. An aryltetralin derivative was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1501238380d719612be54473facd3bb
https://doi.org/10.1071/ch9911307
https://doi.org/10.1071/ch9911307
Autor:
WC Taylor, AR Carroll
Publikováno v:
Australian Journal of Chemistry. 44:1705
On the basis of spectroscopic evidence, the eupomatilones (from eupomatilone-1 to -7) isolated from Eupomatia bennettii F. Muell. were shown to be degraded lignans . Eupomatilone-1 was assigned the structure (1), cis-4-methyl-3-methylene-5-(3″,4″
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d36690379bd2e011c2401f826db652e
https://doi.org/10.1071/ch9911705
https://doi.org/10.1071/ch9911705
Autor:
AR Carroll, WC Taylor
Publikováno v:
Australian Journal of Chemistry. 44:1627
The structures of new extractives from the tubers and aerial parts of Eupomatia bennettii F. Muell. have been assigned as follows: eupomatenoid-15, 2-(4′-methoxyphenyl)-3-methyl-5-(E)-propenylbenzofuran (1); eupomatenoid-16, 7-methoxy-2-(4′-metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a9500fe6fa8bc257fddf4c80ebe1a5d
https://doi.org/10.1071/ch9911627
https://doi.org/10.1071/ch9911627