171 related articles for article (PubMed ID: 19366236)
1. A short and practical synthesis of oseltamivir phosphate (Tamiflu) from (-)-shikimic acid.
Nie LD; Shi XX; Ko KH; Lu WD
J Org Chem; 2009 May; 74(10):3970-3. PubMed ID: 19366236
[TBL] [Abstract][Full Text] [Related]
2. Efficient access to oseltamivir phosphate (Tamiflu) via the O-trimesylate of shikimic acid ethyl ester.
Karpf M; Trussardi R
Angew Chem Int Ed Engl; 2009; 48(31):5760-2. PubMed ID: 19565588
[No Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. Use of the Diels-Alder adduct of pyrrole in organic synthesis. Formal racemic synthesis of Tamiflu.
Kamimura A; Nakano T
J Org Chem; 2010 May; 75(9):3133-6. PubMed ID: 20364872
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Symmetry-based design for the chemoenzymatic synthesis of oseltamivir (Tamiflu) from ethyl benzoate.
Sullivan B; Carrera I; Drouin M; Hudlicky T
Angew Chem Int Ed Engl; 2009; 48(23):4229-31. PubMed ID: 19425033
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Production of shikimic acid.
Ghosh S; Chisti Y; Banerjee UC
Biotechnol Adv; 2012; 30(6):1425-31. PubMed ID: 22445787
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Development of a concise synthesis of (-)-oseltamivir (Tamiflu).
Trost BM; Zhang T
Chemistry; 2011 Mar; 17(13):3630-43. PubMed ID: 21365707
[TBL] [Abstract][Full Text] [Related]
14. Expanding horizons of shikimic acid. Recent progresses in production and its endless frontiers in application and market trends.
Rawat G; Tripathi P; Saxena RK
Appl Microbiol Biotechnol; 2013 May; 97(10):4277-87. PubMed ID: 23553030
[TBL] [Abstract][Full Text] [Related]
15. Synthetic approaches to the neuraminidase inhibitors zanamivir (Relenza) and oseltamivir phosphate (Tamiflu) for the treatment of influenza.
Magano J
Chem Rev; 2009 Sep; 109(9):4398-438. PubMed ID: 19537777
[No Abstract] [Full Text] [Related]
16. A synthesis of oseltamivir (Tamiflu) starting from D-mannitol.
Ko JS; Keum JE; Ko SY
J Org Chem; 2010 Oct; 75(20):7006-9. PubMed ID: 20866058
[TBL] [Abstract][Full Text] [Related]
17. De novo synthesis of Tamiflu via a catalytic asymmetric ring-opening of meso-aziridines with TMSN3.
Fukuta Y; Mita T; Fukuda N; Kanai M; Shibasaki M
J Am Chem Soc; 2006 May; 128(19):6312-3. PubMed ID: 16683784
[TBL] [Abstract][Full Text] [Related]
18. A concise synthesis of (-)-oseltamivir.
Trost BM; Zhang T
Angew Chem Int Ed Engl; 2008; 47(20):3759-61. PubMed ID: 18399551
[No Abstract] [Full Text] [Related]
19. Several generations of chemoenzymatic synthesis of oseltamivir (Tamiflu): evolution of strategy, quest for a process-quality synthesis, and evaluation of efficiency metrics.
Werner L; Machara A; Sullivan B; Carrera I; Moser M; Adams DR; Hudlicky T; Andraos J
J Org Chem; 2011 Dec; 76(24):10050-67. PubMed ID: 22007598
[TBL] [Abstract][Full Text] [Related]
20. Enantioselective Synthesis of Oseltamivir Phosphate (Tamiflu) via the Iron-Catalyzed Stereoselective Olefin Diazidation.
Li H; Shen SJ; Zhu CL; Xu H
J Am Chem Soc; 2018 Aug; 140(33):10619-10626. PubMed ID: 30040881
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]