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Volumn , Issue 7, 2000, Pages 1067-1069

Applications of homoallylic alcohols derived from (-)-sparteine-mediated asymmetric homoaldolization: Entry to 5- to 8-membered unsaturated oxacycles through metathesis reaction

Author keywords

( ) Sparteine; Asymmetric synthesis; Homoaldolization; Oxacycloalkenes; Ring closing metathesis

Indexed keywords

ALCOHOL DERIVATIVE; SPARTEINE;

EID: 0033943965     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (18)

References (39)
  • 2
    • 0030131103 scopus 로고    scopus 로고
    • (b) Faulkner, D. J. Nat. Prod. Rep. 1996, 13, 75. Faulkner, D. J. Nat. Prod. Rep. 2000, 17, 1.
    • (1996) Nat. Prod. Rep. , vol.13 , pp. 75
    • Faulkner, D.J.1
  • 3
    • 0034142130 scopus 로고    scopus 로고
    • (b) Faulkner, D. J. Nat. Prod. Rep. 1996, 13, 75. Faulkner, D. J. Nat. Prod. Rep. 2000, 17, 1.
    • (2000) Nat. Prod. Rep. , vol.17 , pp. 1
    • Faulkner, D.J.1
  • 4
    • 0033516491 scopus 로고    scopus 로고
    • For recent reviews on RCM reactions see: (a) Schrock, R. R. Tetrahedron 1999, 55, 8141.
    • (1999) Tetrahedron , vol.55 , pp. 8141
    • Schrock, R.R.1
  • 8
    • 0034677109 scopus 로고    scopus 로고
    • For recent applications of the RCM methodology to the synthesis of oxacycles and polycyclic ethers: (a) Clark, J. S.; Hamelin, O. Angew: Chem. Int. Ed. 2000, 39, 372.
    • (2000) Angew: Chem. Int. Ed. , vol.39 , pp. 372
    • Clark, J.S.1    Hamelin, O.2
  • 36
    • 0032566021 scopus 로고    scopus 로고
    • ref. 7b
    • For an enhanced reactivity of the RCM reactions by the addition of external Lewis acids in substrates containing ester groups see: ref. 7b, and Ghosh, A. K.; Cappiello, J.; Shin, D. Tetrahedron Lett. 1998, 39, 4651.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 4651
    • Ghosh, A.K.1    Cappiello, J.2    Shin, D.3
  • 37
    • 12344285811 scopus 로고
    • All esters 8a-g were prepared in similar way as described in the above reference. Reaction of the allyl ether 4b gave mixture of products
    • For an application of this strategy in the synthesis of (+)-eldanolide from homoaldol products, see : Paulsen, H.; Hoppe, D. Tetrahedron 1992, 48, 5667. All esters 8a-g were prepared in similar way as described in the above reference. Reaction of the allyl ether 4b gave mixture of products.
    • (1992) Tetrahedron , vol.48 , pp. 5667
    • Paulsen, H.1    Hoppe, D.2
  • 38
    • 0342732795 scopus 로고    scopus 로고
    • note
    • +


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.