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Volumn 46, Issue 17, 2005, Pages 3103-3105

(R)-2,3-Cyclohexylideneglyceraldehyde, a novel template for facile and simple entry into chiral hydroxy γ-lactones: Synthesis of (-)-muricatacin

Author keywords

( ) Muricatacin; (R) 2,3 Cyclohexylideneglyceraldehyde; Functionalized lactones; LiAlH4; Stereodivergent; syn Selective reduction

Indexed keywords

ANNONA MURICATA EXTRACT; GAMMA LACTONE DERIVATIVE; GLYCERALDEHYDE; KETONE; MURICATACIN; UNCLASSIFIED DRUG;

EID: 15944395148     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.03.002     Document Type: Article
Times cited : (30)

References (38)
  • 22
    • 0002874969 scopus 로고
    • J.D. Morrison Academic New York
    • J.W. Scott J.D. Morrison Asymmetric Synthesis Vol. 4 1984 Academic New York 1 226
    • (1984) Asymmetric Synthesis , vol.4 , pp. 1-226
    • Scott, J.W.1
  • 23
  • 29
    • 85030815257 scopus 로고    scopus 로고
    • note
    • 4 reduction: Hydride (0.02 mol) was added to a MeOH solution of 3 (0.02 mol) at 0°C over a period of 10 min and the mixture was stirred at 0°C for 40 min. This was followed by usual work up and isolation of the products
  • 34
    • 85030805688 scopus 로고    scopus 로고
    • note
    • 2Si: C, 77.44; H, 10.06. Found, C, 77.29; H, 10.24
  • 35
    • 85030808214 scopus 로고    scopus 로고
    • note
    • 2Si: C, 78.10; H, 10.41. Found, C, 78.22; H, 10.55


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.