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Volumn 5, Issue 15, 2007, Pages 2413-2422

Regiochemical switching of Mitsunobu cyclisation mode of vicinal diamines with pendant hydroxyl group

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIZATION; REACTION KINETICS; REGIOSELECTIVITY;

EID: 34547201021     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b705081j     Document Type: Article
Times cited : (22)

References (53)
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    • N. Tsuritani K. Yamada N. Yoshikawa M. Shibasaki Chem. Lett. 2002 276
    • (2002) Chem. Lett. , pp. 276
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  • 39
    • 0028147903 scopus 로고
    • Although the TBS protected material could be synthesised in higher yield, deprotection could not be achieved with either TBAF, HF, TFA, CSA, HCO 2H, pTSA
    • R. C. Larock H. Yang S. Weinreb R. J. Herr J. Org. Chem. 1994 59 4172
    • (1994) J. Org. Chem. , vol.59 , pp. 4172
    • Larock, R.C.1    Yang, H.2    Weinreb, S.3    Herr, R.J.4
  • 41
    • 33750456293 scopus 로고
    • S. V. Ley, Oxford, Pergamon Press
    • Comprehensive Organic Synthesis, ed., S. V. Ley, Oxford, Pergamon Press, 1991, vol. 7
    • (1991) Comprehensive Organic Synthesis, Ed. , vol.7
  • 44
    • 0035515394 scopus 로고    scopus 로고
    • The synthesis of aziridines from appropriately substituted 2-aminoethanols has been reported:
    • T. J. Greshock R. L. Funk Org. Lett. 2001 3 3511
    • (2001) Org. Lett. , vol.3 , pp. 3511
    • Greshock, T.J.1    Funk, R.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.