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Volumn 74, Issue 7, 2009, Pages 2858-2861

Regioselective reductive cleavage of bis-benzylidene acetal: Stereoselective synthesis of anticancer agent OGT2378 and glycosidase inhibitor 1,4-dideoxy-1,4-imino-l-xylitol

Author keywords

[No Author keywords available]

Indexed keywords

1,4 DIDEOXY 1,4 IMINO XYLITOL; 2 (HYDROXYMETHYL) 1 PENTYLPIPERIDINE 3,4,5 TRIOL; 2 (HYDROXYMETHYL) 1 TOSYLPYRROLIDINE 3,4 DIOL; 2 (TERTBUTYLDIPHENYLSILYLOXY) 1 (2,2 DIMETHYL 5 OXIRAN 2 YL) 1,3 DIOXOLAN 4 YL)ETHANOL; 4 [(TERTBUTYLDIPHENYLSILYLOXY)METHYL] 2,2 DIMETHYLHEXAHYDRO [1,3]DIOXOLO[4,5 C]PYRIDIN 7 OL; ACETAL DERIVATIVE; AMINO EPOXIDE; ANTINEOPLASTIC AGENT; AZIDO EPOSIDE; BIS BENZYLIDENE ACETAL; GLYCOSIDASE INHIBITOR; N PENTYLDEOXYIDONOJIRIMYCIN; OGT 2378; UNCLASSIFIED DRUG;

EID: 64249155935     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900030p     Document Type: Article
Times cited : (35)

References (53)
  • 1
    • 0034678033 scopus 로고    scopus 로고
    • For reviews and seminal papers on diversity-oriented synthesis, see: a
    • For reviews and seminal papers on diversity-oriented synthesis, see: (a) Schreiber, S. L. Science 2000, 287, 1964.
    • (2000) Science , vol.287 , pp. 1964
    • Schreiber, S.L.1
  • 7
    • 64249123087 scopus 로고    scopus 로고
    • Please see ref 1. For diversity-oriented synthesis of iminosugars see: (a) Lee, B. W, Jeong, I.-Y, Yang, M. S, Choi, S. U, Park, K. H. Synthesis 2000, 1305
    • Please see ref 1. For diversity-oriented synthesis of iminosugars see: (a) Lee, B. W.; Jeong, I.-Y.; Yang, M. S.; Choi, S. U.; Park, K. H. Synthesis 2000, 1305.
  • 13
  • 26
    • 64249169800 scopus 로고    scopus 로고
    • For biological activity, see: (a) ref 5
    • For biological activity, see: (a) ref 5.
  • 33
    • 26944464588 scopus 로고    scopus 로고
    • For highlights, see:, Sept 26
    • (b) For highlights, see: Borman, S. Chem. Eng. News 2005, (Sept 26), 39.
    • (2005) Chem. Eng. News , pp. 39
    • Borman, S.1
  • 36
    • 64249137088 scopus 로고    scopus 로고
    • The first and only synthesis of OGT2378 was reported in the patent literature: Butters, T. D, Dwek, R. A, Fleet C, Orchard, M. G, Piatt, F. M. PCT Int. Appl. WO 2002055498, 2002
    • The first and only synthesis of OGT2378 was reported in the patent literature: Butters, T. D.; Dwek, R. A.; Fleet C.; Orchard, M. G.; Piatt, F. M. PCT Int. Appl. WO 2002055498, 2002.
  • 41
    • 0037450435 scopus 로고    scopus 로고
    • Somfai, P.; Marchand, P.; Torsell, S.; Lindstrom, U. M. Tetrahedron 2003, 59, 1293. cis-Acetonide as well as the corresponding cis- and trans-dibenzyl ether derivatives are known to give a mixture of regioisomers.
    • (b) Somfai, P.; Marchand, P.; Torsell, S.; Lindstrom, U. M. Tetrahedron 2003, 59, 1293. cis-Acetonide as well as the corresponding cis- and trans-dibenzyl ether derivatives are known to give a mixture of regioisomers.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.