메뉴 건너뛰기




Volumn 254, Issue 1-2, 2006, Pages 85-92

Alkoxy group facilitated ring closing metathesis (RCM) of acyclic 1,6-dienes. Facile synthesis of non-racemic highly substituted cyclopentenols

Author keywords

Asymmetric synthesis; Cyclopentenes; Metathesis; Nucleosides

Indexed keywords

ALKYLATION; CATALYSTS; ETHERS; NUCLEIC ACIDS; POLYOLEFINS;

EID: 33745375403     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2006.03.023     Document Type: Article
Times cited : (14)

References (52)
  • 1
    • 33745425391 scopus 로고    scopus 로고
    • For reviews on, RCM reaction see:
  • 29
    • 33745403380 scopus 로고    scopus 로고
    • For reviews on non-metathetic processes see:
  • 32
    • 4143060245 scopus 로고    scopus 로고
    • (a part of this work appeared as a preliminary communication)
    • Nayek A., Banerjee S., Sinha S., and Ghosh S. Tetrahedron Lett. 45 (2004) 6457-6460 (a part of this work appeared as a preliminary communication)
    • (2004) Tetrahedron Lett. , vol.45 , pp. 6457-6460
    • Nayek, A.1    Banerjee, S.2    Sinha, S.3    Ghosh, S.4
  • 33
    • 33745414828 scopus 로고    scopus 로고
    • For recent reviews on the synthesis of carbocyclic nucleosides, see:
  • 36
    • 33745393210 scopus 로고    scopus 로고
    • For selected syntheses of (-)-carbovir see:
  • 47
    • 33745408689 scopus 로고    scopus 로고
    • For a recent approach, see:
  • 49
    • 33745380152 scopus 로고    scopus 로고
    • There is a single report demonstrating that RCM of a 1,6-acyclic diene with acetoxymethyl group at the allylic carbon is faster compared to that of a diene with a hydroxymethyl group


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.