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Volumn 18, Issue 12, 2007, Pages 1419-1427

Enantioselective synthesis of α-benzyloxy-ω-alkenals: application to the synthesis of (+)-exo-brevicomin, (+)-iso-exo-brevicomin, and (-)-isolaurepan

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DERIVATIVE; BREVICOMIN; ISOBREVICOMIN; ISOLAUREPAN; PHEROMONE; UNCLASSIFIED DRUG;

EID: 34447526636     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2007.05.014     Document Type: Article
Times cited : (20)

References (28)
  • 9
    • 20444401234 scopus 로고    scopus 로고
    • For a synthesis of α-methoxy-α-arylacetic acid derivatives involving similar strategy see:
    • For a synthesis of α-methoxy-α-arylacetic acid derivatives involving similar strategy see:. Prasad K.R., and Chandrakumar A. Tetrahedron: Asymmetry 16 (2005) 1897
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 1897
    • Prasad, K.R.1    Chandrakumar, A.2
  • 12
    • 29544431976 scopus 로고    scopus 로고
    • Recent asymmetric synthesis of brevicomin:
    • Recent asymmetric synthesis of brevicomin:. Kumar D.N., and Rao B.V. Tetrahedron Lett. 45 (2004) 2227
    • (2004) Tetrahedron Lett. , vol.45 , pp. 2227
    • Kumar, D.N.1    Rao, B.V.2
  • 19
    • 3042898513 scopus 로고    scopus 로고
    • For a review on the synthesis of pheromones see:
    • For a review on the synthesis of pheromones see:. Mori K. Eur. J. Org. Chem. (1998) 1479
    • (1998) Eur. J. Org. Chem. , pp. 1479
    • Mori, K.1
  • 23
    • 0025600432 scopus 로고
    • Chemo-enzymatic synthesis of threo alcohol 11 is reported in the literature:
    • Chemo-enzymatic synthesis of threo alcohol 11 is reported in the literature:. Matsumoto K., Suzuki N., and Ohta H. Tetrahedron Lett. 31 (1990) 7163
    • (1990) Tetrahedron Lett. , vol.31 , pp. 7163
    • Matsumoto, K.1    Suzuki, N.2    Ohta, H.3
  • 26
    • 34447562546 scopus 로고    scopus 로고
    • note
    • Because of the contamination of benzylbromide, purification of dibenzylether 14 was found to be cumbersome. Hence it was used as such in the next step.
  • 27
    • 0000178030 scopus 로고
    • For enantioselective synthesis of isolaurepan see:
    • For enantioselective synthesis of isolaurepan see:. Kotsuki H., Ushio Y., Kadota I., and Ochi M. J. Org. Chem. 54 (1989) 5153
    • (1989) J. Org. Chem. , vol.54 , pp. 5153
    • Kotsuki, H.1    Ushio, Y.2    Kadota, I.3    Ochi, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.