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Volumn 8, Issue 2, 2013, Pages 488-493

Enantiospecific total synthesis of (-)-bengamide e

Author keywords

anti cancer compounds; metathesis; natural products; polyhydroxy compounds; total synthesis

Indexed keywords

ANTI-CANCER COMPOUNDS; METATHESIS; NATURAL PRODUCTS; POLYHYDROXY COMPOUNDS; TOTAL SYNTHESIS;

EID: 84873817012     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201200999     Document Type: Article
Times cited : (19)

References (33)
  • 32
    • 41649100723 scopus 로고    scopus 로고
    • Addition of 2-lithio-1,3-dithiane to the diamide 17 to produce 16 should be performed strictly under oxygen-free conditions. Contamination of oxygen in the argon or nitrogen used; or presence of oxygen deteriorates the yield of the reaction and the product 16 is obtained only in 41 % yield with a substantial amount of side products that result from 1,3-dithiane. For a cautionary note on the effect of oxygen on the autooxidation of 2-lithio-1,3-dithiane, see
    • K. R. Prasad, S. L. Gholap, J. Org. Chem. 2008, 73, 2916-2919. Addition of 2-lithio-1,3-dithiane to the diamide 17 to produce 16 should be performed strictly under oxygen-free conditions. Contamination of oxygen in the argon or nitrogen used; or presence of oxygen deteriorates the yield of the reaction and the product 16 is obtained only in 41 % yield with a substantial amount of side products that result from 1,3-dithiane. For a cautionary note on the effect of oxygen on the autooxidation of 2-lithio-1,3-dithiane, see
    • (2008) J. Org. Chem. , vol.73 , pp. 2916-2919
    • Prasad, K.R.1    Gholap, S.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.