메뉴 건너뛰기




Volumn , Issue 3, 2012, Pages 438-442

Palladium-catalyzed ring opening of aminocyclopropyl Ugi adducts

Author keywords

aminocyclopropanes; palladium; ring opening; Ugi; Ugi Smiles

Indexed keywords

CYCLOPROPANE DERIVATIVE; ENAMINE; HETEROCYCLIC NITRO COMPOUND; N (4 CHLOROBENZYL) 2 [CYCLOPROPYL(5 IODO 2 ISOPROPYL 6 METHYLPYRIMIDIN 4 YL)AMINO]ACETAMIDE; N (4 CHLOROBENZYL) 2 [ISOPROPYL 4 METHYLPYRIDO[2,3 D]PYRIMIDIN 8(5H) YL]ACETAMIDE; PALLADIUM; UNCLASSIFIED DRUG;

EID: 84856619149     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1290312     Document Type: Article
Times cited : (18)

References (42)
  • 1
    • 0043104432 scopus 로고
    • For reviews on the chemistry of cyclopropanes, see
    • For reviews on the chemistry of cyclopropanes, see:, Danishefshy S, Acc. Chem. Res. 1979 12 66
    • (1979) Acc. Chem. Res. , vol.12 , pp. 66
    • Danishefshy, S.1
  • 6
    • 84856612785 scopus 로고    scopus 로고
    • For Pd-triggered ring opening of alkylidene cyclopropanes, see
    • For Pd-triggered ring opening of alkylidene cyclopropanes, see
  • 34
    • 84890597202 scopus 로고    scopus 로고
    • Zhu J. Bienaymé H. Wiley-VCH Weinheim
    • Multicomponent Reactions Zhu J Bienaymé H Wiley-VCH Weinheim 2005
    • (2005) Multicomponent Reactions
  • 41
    • 84856612786 scopus 로고    scopus 로고
    • The regioselectivity observed with aryl-substituted amino-cyclopropanes may be explained by a productive interaction of the aryl-Pd(II)I intermediate through the less hindered approach of the cyclopropyl ring. Further insights into the potential electronic effects of the aryl moiety should be addressed by comparison with alkyl-substituted cyclo-propanes.
    • The regioselectivity observed with aryl-substituted amino-cyclopropanes may be explained by a productive interaction of the aryl-Pd(II)I intermediate through the less hindered approach of the cyclopropyl ring. Further insights into the potential electronic effects of the aryl moiety should be addressed by comparison with alkyl-substituted cyclo-propanes.
  • 42
    • 80051545816 scopus 로고    scopus 로고
    • A direct Pd-catalyzed activation-functionalization of the C-H bond of cyclopropanes is possible when directing groups are present. For a review, see
    • A direct Pd-catalyzed activation-functionalization of the C-H bond of cyclopropanes is possible when directing groups are present. For a review, see:, Kubota A, Sanford M S., Synthesis 2011 2579
    • (2011) Synthesis , pp. 2579
    • Kubota, A.1    Sanford, M.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.