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Volumn 52, Issue 15, 2011, Pages 1778-1782

Enantioselective synthesis of cyclopropyl δ-lactonealdehydes and dodecyl-5-ene-1-yne-3-ol: Advanced intermediates of solandelactone A and B

Author keywords

Asymmteric hydrogenation; Cyclopropyl lactonealdehydes; Organocatalytic reaction; Oxylipin family; Solandelactone A and B

Indexed keywords

ALDEHYDE DERIVATIVE; CYCLOPROPANE; CYCLOPROPYL DELTA LACTONEALDEHYDE; DODECYL 5 ENE 1 YNE 3 OL; OXYLIPIN; SOLANDELACTONE A; SOLANDELACTONE B; UNCLASSIFIED DRUG;

EID: 79952533458     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.02.008     Document Type: Article
Times cited : (24)

References (37)
  • 28
    • 79952535875 scopus 로고    scopus 로고
    • The enone 7 was conveniently prepared in four steps from 1,7-heptane diol, see Supporting information
    • The enone 7 was conveniently prepared in four steps from 1,7-heptane diol, see Supporting information.
  • 32
    • 79952532459 scopus 로고    scopus 로고
    • note
    • 3Na: 221.1153).
  • 34
    • 79952535565 scopus 로고    scopus 로고
    • note
    • 3Na: 219.0997).
  • 36
    • 79952533881 scopus 로고    scopus 로고
    • Our efforts to isolate keto compound was unsuccessful due to decomposition, hence crude residue was directly subjected to asymmetric transfer hydrogenation
    • Our efforts to isolate keto compound was unsuccessful due to decomposition, hence crude residue was directly subjected to asymmetric transfer hydrogenation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.