메뉴 건너뛰기




Volumn 47, Issue 30, 2006, Pages 5379-5382

Silyl-enolization-asymmetric Claisen rearrangement of 2-allyloxyindolin-3-one: enantioselective total synthesis of 3a-hydroxypyrrolo[2,3-b]indoline alkaloid alline

Author keywords

[No Author keywords available]

Indexed keywords

2 ALLYLOXYINDOLIN 3 ONE; 3A HYDROXYPYRROLO[2,3 B]INDOLINE; ALKALOID DERIVATIVE; AMINE; INDOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33745210993     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.05.124     Document Type: Article
Times cited : (25)

References (37)
  • 19
    • 4344584933 scopus 로고    scopus 로고
    • Recent examples:
    • Recent examples:. Albrecht B.K., and Williams R.M. PNAS 101 (2004) 11949-11954
    • (2004) PNAS , vol.101 , pp. 11949-11954
    • Albrecht, B.K.1    Williams, R.M.2
  • 28
    • 33745188962 scopus 로고    scopus 로고
    • note
    • 4, and evaporated. The residue was purified by silica gel column chromatography (AcOEt-hexane = 1:15) to give 5 as a colorless oil.
  • 29
    • 33745196735 scopus 로고    scopus 로고
    • note
    • 4
  • 30
    • 33745208065 scopus 로고    scopus 로고
    • note
    • O,O′-Disilylated by-product in TBS-silylation of 4 was transformed to O-mono-silylate 6 by treatment with AcOH-MeOH.
  • 34
    • 33745198271 scopus 로고    scopus 로고
    • note
    • 2: C, 74.69; H, 8.48; N, 5.12. Found: C, 74.73; H. 8.60; N, 5.08.
  • 35
    • 0346969633 scopus 로고    scopus 로고
    • The structures of 9 were confirmed by the HMBC cross-peak between the carbonyl carbon and the proton of N-methyl group. This type of transamidation was utilized to the total synthesis of chimonamidine;
    • The structures of 9 were confirmed by the HMBC cross-peak between the carbonyl carbon and the proton of N-methyl group. This type of transamidation was utilized to the total synthesis of chimonamidine;. Takayama H., Matsuda Y., Masubuchi K., Ishida A., Kitajima M., and Aimi N. Tetrahedron 60 (2004) 893-900
    • (2004) Tetrahedron , vol.60 , pp. 893-900
    • Takayama, H.1    Matsuda, Y.2    Masubuchi, K.3    Ishida, A.4    Kitajima, M.5    Aimi, N.6
  • 36
    • 33745192106 scopus 로고    scopus 로고
    • note
    • 3CN.
  • 37
    • 33745196284 scopus 로고    scopus 로고
    • note
    • 9a


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.