The synthesis of (4S,5S)-(-)-isocytoxazone

Tetrahedron Asymmetry

Volumn 20, Issue 17, 2009, Pages 2048-2051

  Rozwadowska, Maria D ^a   Tomczak, Anna ^a  

^a ADAM MICKIEWICZ UNIVERSITY   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINO 1 (4 METHOXYPHENYL) 1,3 PROPANEDIOL; 2 AMINO 1 (4 NITROPHENYL) 1,3 PROPANEDIOL; 2 N,N DIBENZYLAMINO 1 (4 AMINOPHENYL) 1,3 PROPANEDIOL; 2 N,N DIBENZYLAMINO 1 (4 IODOPHENYL) 1,3 PROPANEDIOL; 2 N,N DIBENZYLAMINO 1 (4 METHOXYPHENYL) 1,3 PROPANEDIOL; 2 N,N DIBENZYLAMINO 1 (4 NITROPHENYL) 1,3 PROPANEDIOL; 2 TERT BUTOXYCARBONYLAMINO 1 (4 METHOXYPHENYL) 1,3 PROPANEDIOL; 4 HYDROXYMETHYL 5 (4 METHOXYPHENYL)OXAZOLIDIN 2 ONE [ISOCYTOXAZONE]; 4 METHOXYPHENYL AMINO DIOL; ISOCYTOXAZONE; N BOC DERIVATIVE; NATURAL PRODUCT; PROPANEDIOL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CONTROLLED STUDY; CYCLIZATION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SUBSTITUTION REACTION; SYNTHESIS;

EID: 70349226768     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.07.034     Document Type: Article

References (21)

1. Kakeya H., Morishita M., Kobinta K., Osono M., Ishizuka M., and Osada H. J. Antibiot. 51 (1998) 1126-1128
2. Carter P.H., LaPorte J.R., Scherle P.A., and Decicco C.P. Bioorg. Med. Chem. Lett. 13 (2003) 1237-1239
3. Kumar A.R., Bhaskar G., Madhan A., and Rao B.V. Synth. Commun. 33 (2003) 2907-2916
4. Grajewska A., and Rozwadowska M.D. Tetrahedron: Asymmetry 18 (2007) 803-813
5. Giorgio E., Viglione R.G., Zanasi R., and Rosini C. J. Am. Chem. Soc. 126 (2004) 12968-12976
6. Giorgio E., Roje M., Tanaka K., Hamersak Z., Sunjic V., Nakanishi K., Rosini C., and Berova N. J. Org. Chem. 70 (2005) 6557-6563
7. Kakeya H., Morishita M., Koshino H., Morita T., Kobayashi K., and Osada H. J. Org. Chem. 64 (1999) 1052-1053
8. Hamersak Z., Sepac D., Ziher D., and Sunjic V. Synthesis (2003) 375-382
9. Cardillo G., De Simone A., Gentilucci L., and Tomasini C. J. Chem. Soc., Chem. Commun, (1994) 735-736
10. Moreno-Manas M., and Padros I. J. Heterocycl. Chem. 30 (1993) 1235-1239
11. Mitchell S.A., Oates B.D., Razavi H., and Polt R. J. Org. Chem. 63 (1998) 8837-8842
12. Cwik A., Fuchs A., Hell Z., Bojtos I., Halmai D., and Bombicz P. Org. Biomol. Chem. 3 (2005) 967-969
13. Grajewska A., Rozwadowska M.D., and Gzella A. Polish J. Chem. 81 (2007) 1861-1868
14. Metro T.-X., Pardo D.G., and Cossy J. J. Org. Chem. 73 (2008) 707-710
15. Satoh T., Mitsuo N., Nishiki M., Inoue Y., and Ooi Y. Chem. Pharm. Bull. 29 (1981) 1143-1445
16. Krasnokutskaya E.A., Semenischeva N.I., Filimonov V.D., and Knochel P. Synthesis (2007) 81-84
17. Wolter M., Nordmann G., Job G.E., and Buchwald S.L. Org. Lett. 4 (2002) 973-976
18. Altman R.A., Shafir A., Choi A., Lichtor P.A., and Buchwald S.L. J. Org. Chem. 73 (2008) 284-286
19. Page P.C.B., Buckley B.R., Rassias G.A., and Blacker A.J. Eur. J. Org. Chem. (2006) 803-813
20. Jia X., Huang Q., Li J., Li S., and Yang Q. Synlett (2007) 806-808
21. Jiang B., and Si Y.-G. Adv. Synth. Catal. 346 (2004) 669-674