메뉴 건너뛰기




Volumn 53, Issue 38, 1997, Pages 12933-12946

Palladium-catalyzed reductive ring opening with formic acid of aziridines bearing an α,β-unsaturated ester group

Author keywords

[No Author keywords available]

Indexed keywords

AZIRIDINE DERIVATIVE;

EID: 0030767529     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00817-X     Document Type: Article
Times cited : (19)

References (48)
  • 27
    • 0000746108 scopus 로고
    • The term "activated aziridines" has been introduced by Ham for aziridines that easily undergo nucleophilic SN2-type ring-opening. Ham, G. E. J. Org. Chem. 1964, 29, 3052.
    • (1964) J. Org. Chem. , vol.29 , pp. 3052
    • Ham, G.E.1
  • 31
    • 0000315403 scopus 로고
    • Deprotection of arenesulfonamides with Sml2, see Vedejs, E.; Lin, S. J. Org. Chem. 1994, 59, 1602.
    • (1994) J. Org. Chem. , vol.59 , pp. 1602
    • Vedejs, E.1    Lin, S.2
  • 39
    • 0001177322 scopus 로고
    • For catalytic asymmetric reductions of allylic esters with formic acid, see Hayashi, T.; Iwamura, H.:, Naito, M.; Matsumoto, Y.; Uozumi, Y. J. Am. Chem. Soc. 1994, 116, 775. Hayashi, T.; Kawatsura, M.; Iwamura, H.; Yamaura, Y.; Uozumi, Y. Chem. Commun. 1996, 1767.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 775
    • Hayashi, T.1    Iwamura, H.2    Naito, M.3    Matsumoto, Y.4    Uozumi, Y.5
  • 40
    • 0001916342 scopus 로고    scopus 로고
    • For catalytic asymmetric reductions of allylic esters with formic acid, see Hayashi, T.; Iwamura, H.:, Naito, M.; Matsumoto, Y.; Uozumi, Y. J. Am. Chem. Soc. 1994, 116, 775. Hayashi, T.; Kawatsura, M.; Iwamura, H.; Yamaura, Y.; Uozumi, Y. Chem. Commun. 1996, 1767.
    • (1996) Chem. Commun. , pp. 1767
    • Hayashi, T.1    Kawatsura, M.2    Iwamura, H.3    Yamaura, Y.4    Uozumi, Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.