메뉴 건너뛰기




Volumn 70, Issue 18, 2005, Pages 7133-7148

Silatropic carbonyl ene cyclizations in the synthesis of pseudosugars and hydroxylated piperidines

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDES; HYDROXYLATION; NITROGEN; ORGANIC ACIDS; SILICON; SYNTHESIS (CHEMICAL);

EID: 24144459555     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050644v     Document Type: Article
Times cited : (11)

References (40)
  • 3
    • 0000540593 scopus 로고
    • For early studies on silatropic processes see: (a) Slutsky, J.; Kwart, H. J. Am. Chem. Soc. 1973, 95, 8678-8685.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 8678-8685
    • Slutsky, J.1    Kwart, H.2
  • 5
    • 11844267184 scopus 로고    scopus 로고
    • For a recent theoretical treatment supporting the concerted silatropic ene mechanism in the uncatalysed Mukaiyama aldol reaction see: (c) Wong, C. T.; Wong, M. W. J. Org. Chem. 2005, 70, 124-131.
    • (2005) J. Org. Chem. , vol.70 , pp. 124-131
    • Wong, C.T.1    Wong, M.W.2
  • 7
    • 33645585078 scopus 로고    scopus 로고
    • Phil. Thesis, University of Oxford, Oxford, U.K.
    • Hall, M. J. D.Phil. Thesis, University of Oxford, Oxford, U.K., 2003.
    • (2003)
    • Hall, M.J.D.1
  • 15
    • 33645594114 scopus 로고    scopus 로고
    • Unpublished results
    • Robertson, J.; Tyrrell, A. T. Unpublished results, 2004. See also ref3.
    • (2004)
    • Robertson, J.1    Tyrrell, A.T.2
  • 16
    • 77957047686 scopus 로고    scopus 로고
    • Advances in chemical synthesis of carbasugars and analogues
    • Atta-ur-Rahman, Ed.; Elsevier: Amsterdam
    • (a) Rassu, G.; Auzzas, L.; Pinna, L.; Battistini, L.; Curti, C. Advances in Chemical Synthesis of Carbasugars and Analogues. In Studies in Natural Products Chemistry, Vol. 29, Part J; Atta-ur-Rahman, Ed.; Elsevier: Amsterdam, 2003, 449-520.
    • (2003) Studies in Natural Products Chemistry , vol.29 , Issue.PART J , pp. 449-520
    • Rassu, G.1    Auzzas, L.2    Pinna, L.3    Battistini, L.4    Curti, C.5
  • 33
    • 33645602339 scopus 로고    scopus 로고
    • note
    • For example, application of Piers' protocol (ref 7a) to (S)-ethyl lactate and silane 34 led only to (S)-ethyl O-(phenyl)lactate in low yield.
  • 35
    • 33645599874 scopus 로고    scopus 로고
    • note
    • int = 0.02), 1655 reflections used, final wR = 0.0664.
  • 39
    • 33645598511 scopus 로고    scopus 로고
    • Phil. Thesis, University of Oxford, Oxford, U.K.
    • Stafford, P. M. D.Phil. Thesis, University of Oxford, Oxford, U.K., 2004.
    • (2004)
    • Stafford, P.M.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.