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Volumn , Issue 19, 2006, Pages 4435-4439

Stereoselective disposition of the geminal dimethyl group in the cyclization of geranyl acetate under zeolite confinement conditions

Author keywords

Catalysis; Cyclization; Stereoselectivity; Terpenes; Zeolites

Indexed keywords


EID: 33749434934     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200600367     Document Type: Article
Times cited : (9)

References (38)
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    • Angew. Chem. Int. Ed. 2000, 39, 2812-2833;
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    • and references therein
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    • (1993) Pure Appl. Chem. , vol.65 , pp. 1329-1336
    • Vlad, P.F.1
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    • Angew. Chem. Int. Ed. 2005, 44, 1924-1942.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 1924-1942
  • 23
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    • Chem. Abstr. 1973, 79, 77795.
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  • 33
    • 33749427337 scopus 로고    scopus 로고
    • note
    • 2O.
  • 34
    • 33749452637 scopus 로고    scopus 로고
    • note
    • [3]).
  • 36
    • 0000311233 scopus 로고    scopus 로고
    • b) C. Fehr, Angew. Chem. 1998, 110, 2509-2512;
    • (1998) Angew. Chem. , vol.110 , pp. 2509-2512
    • Fehr, C.1
  • 37
    • 0032544497 scopus 로고    scopus 로고
    • 2OAc resonates at δ = 0.94 ppm, and the trans one at δ = 0.92 ppm. Moreover, from a combination of DEPT and 2D-NMR techniques it was found that the tertiary allylic hydrogen atom of la resonates at δ = 2.16 ppm and that of lb at δ = 1.72 ppm.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2407-2409
  • 38
    • 33749448483 scopus 로고    scopus 로고
    • note
    • -1 between two transition states reflects a product ratio of around 80:20.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.