메뉴 건너뛰기




Volumn 3, Issue 16, 2001, Pages 2537-2538

Gold(III) chloride catalyzed cyclization of α-hydroxyallenes to 2,5-dihydrofurans

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE;

EID: 0000177104     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016205+     Document Type: Article
Times cited : (306)

References (21)
  • 3
    • 0345476898 scopus 로고    scopus 로고
    • (b) Evans, P. A.; Murthy, V. S.; Roseman, J. D.; Rheingold, A. L. Angew. Chem. 1999, 111, 3370-3372; Angew. Chem., Int. Ed. Engl. 1999, 38, 3175-3177.
    • (1999) Angew. Chem., Int. Ed. Engl. , vol.38 , pp. 3175-3177
  • 7
    • 0019164421 scopus 로고
    • (b) Franck, B.; Gehrken, H.-P. Angew. Chem. 1980, 92, 484-486; Angew. Chem., Int. Ed. Engl. 1980, 19, 461-462.
    • (1980) Angew. Chem. , vol.92 , pp. 484-486
    • Franck, B.1    Gehrken, H.-P.2
  • 8
    • 0018816736 scopus 로고
    • (b) Franck, B.; Gehrken, H.-P. Angew. Chem. 1980, 92, 484-486; Angew. Chem., Int. Ed. Engl. 1980, 19, 461-462.
    • (1980) Angew. Chem., Int. Ed. Engl. , vol.19 , pp. 461-462
  • 11
    • 0034728954 scopus 로고    scopus 로고
    • Recently, similar cyclizations of secondary allylic alcohols have been reported: (a) Young, J.-j.; Jung, L.-j.; Chen, K.-m. Tetrahedron Lett. 2000, 41, 3411-3413.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 3411-3413
    • Young, J.-J.1    Jung, L.-J.2    Chen, K.-M.3
  • 14
    • 0034600902 scopus 로고    scopus 로고
    • (a) Hashmi, A. S. K.; Schwarz, L.; Choi, J.-H.; Frost, T. M. Angew. Chem. 2000, 112, 2382-2385; Angew. Chem., Int. Ed. 2000, 39, 2285-2288.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 2285-2288
  • 15
    • 0000524295 scopus 로고    scopus 로고
    • (b) Hashmi, A. S. K. Angew. Chem. 2000, 112, 3737-3740; Angew. Chem., Int. Ed. 2000, 39, 3590-3593.
    • (2000) Angew. Chem. , vol.112 , pp. 3737-3740
    • Hashmi, A.S.K.1
  • 16
    • 0034675566 scopus 로고    scopus 로고
    • (b) Hashmi, A. S. K. Angew. Chem. 2000, 112, 3737-3740; Angew. Chem., Int. Ed. 2000, 39, 3590-3593.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3590-3593
  • 19
    • 33751158290 scopus 로고
    • (c) The following protocol was found to be superior in most cases: Marshall, J. A.; Bartley, G. S. J. Org. Chem. 1994, 59, 7169-7171.
    • (1994) J. Org. Chem. , vol.59 , pp. 7169-7171
    • Marshall, J.A.1    Bartley, G.S.2
  • 21
    • 0042724535 scopus 로고    scopus 로고
    • note
    • With the more Lewis acid labile trimethylsilyl or triethylsilyl ether, however, no cyclization but cleavage of the protection group was observed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.