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Volumn 9, Issue 2, 2007, Pages 247-250

Synthesis of protected chiral vicinal diaminoalcohols by diastereoselective intramolecular benzylic substitution from bistrichloroacetimidates

Author keywords

[No Author keywords available]

Indexed keywords

AMINOALCOHOL; DRUG DERIVATIVE; IMIDE; TRICHLOROACETIC ACID;

EID: 33846599336     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0627202     Document Type: Article
Times cited : (18)

References (42)
  • 20
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    • For a metal-catalyzed enantioselective version, see
    • For a metal-catalyzed enantioselective version, see: Anderson, C. E.; Overman, L. E. J. Am. Chem. Soc. 2003, 125, 12412-12413.
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 12412-12413
    • Anderson, C.E.1    Overman, L.E.2
  • 29
    • 0000763561 scopus 로고    scopus 로고
    • (b) Reetz, M. T. Chem. Rev. 1999, 99, 1121-1162.
    • (1999) Chem. Rev , vol.99 , pp. 1121-1162
    • Reetz, M.T.1
  • 30
    • 17844404512 scopus 로고    scopus 로고
    • For diastereoselective and stereodivergent three-component phenolic Mannich reactions, see
    • For diastereoselective and stereodivergent three-component phenolic Mannich reactions, see: Rondot, C.; Zhu, J. Org. Lett. 2005, 7, 1641-1644.
    • (2005) Org. Lett , vol.7 , pp. 1641-1644
    • Rondot, C.1    Zhu, J.2
  • 31
    • 0032481080 scopus 로고    scopus 로고
    • The bistrichloroacetimidates of olefinic 1,3-diols and olefinic 1,2-diols have been prepared and used in iodine-promoted cyclization. Under these conditions, these bistrichloroacetimidates displayed completely different reactivity from that shown in the present study. See: (a) Kang, S. H.; Kim, J. S.; Youn, J.-K. Tetrahedron Lett. 1998, 39, 9047-9050.
    • The bistrichloroacetimidates of olefinic 1,3-diols and olefinic 1,2-diols have been prepared and used in iodine-promoted cyclization. Under these conditions, these bistrichloroacetimidates displayed completely different reactivity from that shown in the present study. See: (a) Kang, S. H.; Kim, J. S.; Youn, J.-K. Tetrahedron Lett. 1998, 39, 9047-9050.
  • 37
    • 0036642529 scopus 로고    scopus 로고
    • For a recent comprehensive review in the field, see
    • (a) For a recent comprehensive review in the field, see: Van De Water, R. W.; Pettus, T. R. R. Tetrahedron 2002, 58, 5367-5405.
    • (2002) Tetrahedron , vol.58 , pp. 5367-5405
    • Van De Water, R.W.1    Pettus, T.R.R.2
  • 42
    • 0036558479 scopus 로고    scopus 로고
    • For a recent comprehensive review in the field, see
    • For a recent comprehensive review in the field, see: Scott, J. D.; Williams, R. M. Chem. Rev. 2002, 102, 1669-1730.
    • (2002) Chem. Rev , vol.102 , pp. 1669-1730
    • Scott, J.D.1    Williams, R.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.