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Volumn 44, Issue 28, 2003, Pages 5289-5292

A concise and general methodology for the complete asymmetric synthesis of the orthogonally protected 2-amino-1,3,4-butanetriols (ABTs)

Author keywords

2 amino 1,3,4 butanetriols; Mitsunobu reaction; Oxazoline; Regioselective aminohydroxylation

Indexed keywords

2 AMINO 1,3,4 BUTANETRIOL; ALKENE; AMINOALCOHOL; CARBON; HYDROXYL GROUP; OXAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037670092     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)01208-5     Document Type: Article
Times cited : (12)

References (49)
  • 10
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    • Iminosugars as Glycosidase Inhihitors: Nojirimycin and Beyond; Stutz
    • Esumi Y., Suzuki Y., Kimura K., Yoshihama M., Ichikawa T., Uramoto M. J. Antibiot. 52:1999;281 Iminosugars as Glycosidase Inhihitors: Nojirimycin and Beyond; Stutz, A. E., Ed.; Wiley-VCH: Weinheim, 1999.
    • (1999) J. Antibiot. , vol.52 , pp. 281
    • Esumi, Y.1    Suzuki, Y.2    Kimura, K.3    Yoshihama, M.4    Ichikawa, T.5    Uramoto, M.6
  • 37
    • 0033576420 scopus 로고    scopus 로고
    • For other similar approaches, see: (b) Morgan, A. J.; Masse, C. E.; Panek, J. S. Org. Lett. 1999, 1, 1949; (c) Chuang, C.-C.; Vassar, V.; Ma, Z.; Geney, R.; Ojima, I. Chirality 2002, 14, 151.
    • (1999) Org. Lett. , vol.1 , pp. 1949
    • Morgan, A.J.1    Masse, C.E.2    Panek, J.S.3
  • 38
    • 0036152266 scopus 로고    scopus 로고
    • For other similar approaches, see: (b) Morgan, A. J.; Masse, C. E.; Panek, J. S. Org. Lett. 1999, 1, 1949; (c) Chuang, C.-C.; Vassar, V.; Ma, Z.; Geney, R.; Ojima, I. Chirality 2002, 14, 151.
    • (2002) Chirality , vol.14 , pp. 151
    • Chuang, C.-C.1    Vassar, V.2    Ma, Z.3    Geney, R.4    Ojima, I.5
  • 44
    • 0001701976 scopus 로고    scopus 로고
    • To prepare the N-Boc protected 6 directly from 1, the AA reaction of 1 with N-chloro-tert-butyl carbamate was attempted. However, the reaction suffered from a poor reaction yield, and further the desired product and tert-butyl carbamate could not be separated by column
    • Burk M.J., Allen J.G. J. Org. Chem. 62:1997;7054 To prepare the N-Boc protected 6 directly from 1, the AA reaction of 1 with N-chloro-tert-butyl carbamate was attempted. However, the reaction suffered from a poor reaction yield, and further the desired product and tert-butyl carbamate could not be separated by column.
    • (1997) J. Org. Chem. , vol.62 , pp. 7054
    • Burk, M.J.1    Allen, J.G.2
  • 49
    • 85031158764 scopus 로고    scopus 로고
    • note
    • 3) δ: 155.42, 153.92, 152.66, 138.30, 135.70, 135.58, 133.12, 133.00, 129.69, 128.27, 127.78, 127.70, 127.66, 127.48, 115.51, 114.59, 79.19, 78.34, 72.70, 67.49, 64.72, 55.65, 50.75, 28.29, 26.81, 19.10.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.