107 related articles for article (PubMed ID: 20866058)
1. 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]
2. 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]
3. Second generation catalytic asymmetric synthesis of Tamiflu: allylic substitution route.
Mita T; Fukuda N; Roca FX; Kanai M; Shibasaki M
Org Lett; 2007 Jan; 9(2):259-62. PubMed ID: 17217279
[TBL] [Abstract][Full Text] [Related]
4. Synthesis of (-)-oseltamivir phosphate (Tamiflu) starting from cis-2,3-bis(hydroxymethyl)aziridine.
Oh HS; Kang HY
J Org Chem; 2012 Oct; 77(19):8792-6. PubMed ID: 22970883
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. Formal total synthesis of (-)-oseltamivir phosphate.
Tanaka T; Tan Q; Kawakubo H; Hayashi M
J Org Chem; 2011 Jul; 76(13):5477-9. PubMed ID: 21627156
[TBL] [Abstract][Full Text] [Related]
12. Two approaches toward the formal total synthesis of oseltamivir phosphate (Tamiflu): catalytic enantioselective three-component reaction strategy and L-glutamic acid strategy.
Alagiri K; Furutachi M; Yamatsugu K; Kumagai N; Watanabe T; Shibasaki M
J Org Chem; 2013 Apr; 78(8):4019-26. PubMed ID: 23517385
[TBL] [Abstract][Full Text] [Related]
13. Efficient short step synthesis of Corey's tamiflu intermediate.
Kipassa NT; Okamura H; Kina K; Hamada T; Iwagawa T
Org Lett; 2008 Mar; 10(5):815-6. PubMed ID: 18220405
[TBL] [Abstract][Full Text] [Related]
14. An aldol approach to the enantioselective synthesis of (-)-oseltamivir phosphate.
Trajkovic M; Ferjancic Z; Saicic RN
Org Biomol Chem; 2011 Oct; 9(20):6927-9. PubMed ID: 21894312
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. Sugar-based synthesis of Tamiflu and its inhibitory effects on cell secretion.
Ma J; Zhao Y; Ng S; Zhang J; Zeng J; Than A; Chen P; Liu XW
Chemistry; 2010 Apr; 16(15):4533-40. PubMed ID: 20217875
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]