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Volumn 49, Issue 20, 2008, Pages 3326-3329

Stereoinduced cyclization of acyloxyalkenes using iodosylbenzene via a 1,3-dioxan-2-yl cation

Author keywords

Hypervalent iodine; Iodosylbenzene; Neighboring group participation; Tetrahydrofuran

Indexed keywords

3 ACYLOXY 5 METHYL 2 SILYLTETRAHYDROFURAN DERIVATIVE; 4 ACYCLOXY 2 METHYLTETRAHYDROFURAN; ACYLOXYLALKENE DERIVATIVE; ALKENE DERIVATIVE; CARBOXYLIC ACID; CATION; EPOXIDE; IODOSOBENZENE; TETRAHYDROFURAN; UNCLASSIFIED DRUG;

EID: 42149107381     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.03.010     Document Type: Article
Times cited : (8)

References (49)
  • 3
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    • Wirth T. (Ed), Springer, Berlin
    • In: Wirth T. (Ed). Hypervalent Iodine Chemistry (2003), Springer, Berlin
    • (2003) Hypervalent Iodine Chemistry
  • 4
    • 0031027260 scopus 로고    scopus 로고
    • For recent reviews, see:
    • For recent reviews, see:. Varvoglis A. Tetrahedron 53 (1997) 1179-1255
    • (1997) Tetrahedron , vol.53 , pp. 1179-1255
    • Varvoglis, A.1
  • 32
    • 33645947338 scopus 로고    scopus 로고
    • For a related paper, see:
    • For a related paper, see:. Fujita M., Lee H.J., and Okuyama T. Org. Lett. 8 (2006) 1399-1401
    • (2006) Org. Lett. , vol.8 , pp. 1399-1401
    • Fujita, M.1    Lee, H.J.2    Okuyama, T.3
  • 33
    • 42149089976 scopus 로고    scopus 로고
    • Oxidative cyclization of pent-4-en-2-ol leading to 4-hydroxy-2-methyltetrahydrofuran has been achieved by titanium silicate-1 catalysis. The trans/cis ratio of the tetrahydrofuran product was 72:28.
    • Oxidative cyclization of pent-4-en-2-ol leading to 4-hydroxy-2-methyltetrahydrofuran has been achieved by titanium silicate-1 catalysis. The trans/cis ratio of the tetrahydrofuran product was 72:28.
  • 42
    • 42149115804 scopus 로고    scopus 로고
    • 9c
    • 9c
  • 45
    • 42149112313 scopus 로고    scopus 로고
    • 10b may make the generation of an α-silyl carbocation possible.
    • 10b may make the generation of an α-silyl carbocation possible.
  • 47
    • 42149167435 scopus 로고    scopus 로고
    • 11b,c Our approach to 2-silyltetrahydrofurans is complementary to the 3+2 cycloaddition for selective preparations of silyl-substituted tetrahydrofurans.
    • 11b,c Our approach to 2-silyltetrahydrofurans is complementary to the 3+2 cycloaddition for selective preparations of silyl-substituted tetrahydrofurans.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.