246 related articles for article (PubMed ID: 20859964)
1. High-yielding synthesis of the anti-influenza neuraminidase inhibitor (-)-oseltamivir by two "one-pot" sequences.
Ishikawa H; Suzuki T; Orita H; Uchimaru T; Hayashi Y
Chemistry; 2010 Nov; 16(42):12616-26. PubMed ID: 20859964
[TBL] [Abstract][Full Text] [Related]
2. High-yielding synthesis of the anti-influenza neuramidase inhibitor (-)-oseltamivir by three "one-pot" operations.
Ishikawa H; Suzuki T; Hayashi Y
Angew Chem Int Ed Engl; 2009; 48(7):1304-7. PubMed ID: 19123206
[TBL] [Abstract][Full Text] [Related]
3. A practical and azide-free synthetic approach to oseltamivir from diethyl D-tartrate.
Weng J; Li YB; Wang RB; Li FQ; Liu C; Chan AS; Lu G
J Org Chem; 2010 May; 75(9):3125-8. PubMed ID: 20394411
[TBL] [Abstract][Full Text] [Related]
4. One-pot synthesis of (-)-oseltamivir and mechanistic insights into the organocatalyzed Michael reaction.
Mukaiyama T; Ishikawa H; Koshino H; Hayashi Y
Chemistry; 2013 Dec; 19(52):17789-800. PubMed ID: 24249709
[TBL] [Abstract][Full Text] [Related]
5. Time Economical Total Synthesis of (-)-Oseltamivir.
Hayashi Y; Ogasawara S
Org Lett; 2016 Jul; 18(14):3426-9. PubMed ID: 27378379
[TBL] [Abstract][Full Text] [Related]
6. One-Pot Synthesis of (S)-Baclofen via Aldol Condensation of Acetaldehyde with Diphenylprolinol Silyl Ether Mediated Asymmetric Michael Reaction as a Key Step.
Hayashi Y; Sakamoto D; Okamura D
Org Lett; 2016 Jan; 18(1):4-7. PubMed ID: 26636719
[TBL] [Abstract][Full Text] [Related]
7. Different synthetic strategies of oseltamivir phosphate: a potent influenza neuraminidase inhibitor.
Gong J; Xu W
Curr Med Chem; 2008; 15(30):3145-59. PubMed ID: 19075659
[TBL] [Abstract][Full Text] [Related]
8. Biotin-, fluorescein- and 'clickable' conjugates of phospha-oseltamivir as probes for the influenza virus which utilize selective binding to the neuraminidase.
Stanley M; Martin SR; Birge M; Carbain B; Streicher H
Org Biomol Chem; 2011 Aug; 9(16):5625-9. PubMed ID: 21720632
[TBL] [Abstract][Full Text] [Related]
9. Diphenylprolinol silyl ether catalysis in an asymmetric formal carbo [3 + 3] cycloaddition reaction via a domino Michael/Knoevenagel condensation.
Hayashi Y; Toyoshima M; Gotoh H; Ishikawa H
Org Lett; 2009 Jan; 11(1):45-8. PubMed ID: 19053718
[TBL] [Abstract][Full Text] [Related]
10. Diphenylprolinol silyl ether catalyzed asymmetric Michael reaction of nitroalkanes and β,β-disubstituted α,β-unsaturated aldehydes for the construction of all-carbon quaternary stereogenic centers.
Hayashi Y; Kawamoto Y; Honda M; Okamura D; Umemiya S; Noguchi Y; Mukaiyama T; Sato I
Chemistry; 2014 Sep; 20(38):12072-82. PubMed ID: 25164711
[TBL] [Abstract][Full Text] [Related]
11. Stereoisomers of oseltamivir - synthesis, in silico prediction and biological evaluation.
Hajzer V; Fišera R; Latika A; Durmis J; Kollár J; Frecer V; Tučeková Z; Miertuš S; Kostolanský F; Varečková E; Šebesta R
Org Biomol Chem; 2017 Feb; 15(8):1828-1841. PubMed ID: 28155963
[TBL] [Abstract][Full Text] [Related]
12. Divalent oseltamivir analogues as potent influenza neuraminidase inhibitors.
Yan ZL; Liu AY; Wei XX; Zhang Z; Qin L; Yu Q; Yu P; Lu K; Yang Y
Carbohydr Res; 2019 May; 477():32-38. PubMed ID: 30954773
[TBL] [Abstract][Full Text] [Related]
13. Synthesis of tamiflu and its phosphonate congeners possessing potent anti-influenza activity.
Shie JJ; Fang JM; Wang SY; Tsai KC; Cheng YS; Yang AS; Hsiao SC; Su CY; Wong CH
J Am Chem Soc; 2007 Oct; 129(39):11892-3. PubMed ID: 17850083
[No Abstract] [Full Text] [Related]
14. Efficient formal synthesis of oseltamivir phosphate (Tamiflu) with inexpensive D-ribose as the starting material.
Osato H; Jones IL; Chen A; Chai CL
Org Lett; 2010 Jan; 12(1):60-3. PubMed ID: 19938847
[TBL] [Abstract][Full Text] [Related]
15. Asymmetric Michael reaction of acetaldehyde catalyzed by diphenylprolinol silyl ether.
Hayashi Y; Itoh T; Ohkubo M; Ishikawa H
Angew Chem Int Ed Engl; 2008; 47(25):4722-4. PubMed ID: 18435523
[No Abstract] [Full Text] [Related]
16. A short enantioselective pathway for the synthesis of the anti-influenza neuramidase inhibitor oseltamivir from 1,3-butadiene and acrylic acid.
Yeung YY; Hong S; Corey EJ
J Am Chem Soc; 2006 May; 128(19):6310-1. PubMed ID: 16683783
[TBL] [Abstract][Full Text] [Related]
17. Synthesis of the anti-influenza agent (-)-oseltamivir free base and (-)-methyl 3-epi-shikimate.
Rawat V; Dey S; Sudalai A
Org Biomol Chem; 2012 May; 10(20):3988-90. PubMed ID: 22522650
[TBL] [Abstract][Full Text] [Related]
18. Inhibitor selectivity of a new class of oseltamivir analogs against viral neuraminidase over human neuraminidase enzymes.
Albohy A; Mohan S; Zheng RB; Pinto BM; Cairo CW
Bioorg Med Chem; 2011 May; 19(9):2817-22. PubMed ID: 21489803
[TBL] [Abstract][Full Text] [Related]
19. New, efficient synthesis of oseltamivir phosphate (Tamiflu) via enzymatic desymmetrization of a meso-1,3-cyclohexanedicarboxylic acid diester.
Zutter U; Iding H; Spurr P; Wirz B
J Org Chem; 2008 Jul; 73(13):4895-902. PubMed ID: 18517254
[TBL] [Abstract][Full Text] [Related]
20. A synthesis of Tamiflu by using a barium-catalyzed asymmetric Diels-Alder-type reaction.
Yamatsugu K; Yin L; Kamijo S; Kimura Y; Kanai M; Shibasaki M
Angew Chem Int Ed Engl; 2009; 48(6):1070-6. PubMed ID: 19016287
[No Abstract] [Full Text] [Related]
[Next] [New Search]
