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Volumn 126, Issue 39, 2004, Pages 12250-12251

Alkenes from terminal epoxides using lithium 2,2,6,6-tetramethylpiperidide and organolithiums or Grignard reagents

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; ALLYL COMPOUND; EPOXIDE; LITHIUM 2,2,6,6 TETRAMETHYLPIPERIDINE; ORGANOLITHIUM COMPOUND; PIPERIDINE DERIVATIVE; SILANE DERIVATIVE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

EID: 4644306525     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja045513a     Document Type: Article
Times cited : (36)

References (17)
  • 3
    • 4644283785 scopus 로고    scopus 로고
    • note
    • See Supporting Information.
  • 9
    • 4644270929 scopus 로고    scopus 로고
    • note
    • The geometry of the homoallylic alcohols confirmed the geometrical integrity of the alkenyllithiums used.
  • 10
    • 0842299374 scopus 로고    scopus 로고
    • Fleming, I., Ed.; Thieme: Stuttgart
    • Sarkar, T. K. In Science of Synthesis: Fleming, I., Ed.; Thieme: Stuttgart, 2001; Vol. 4, pp 837-925.
    • (2001) Science of Synthesis , vol.4 , pp. 837-925
    • Sarkar, T.K.1
  • 12
    • 4644270725 scopus 로고    scopus 로고
    • note
    • Use of hexane led to lower stereoselectivities.
  • 13
    • 4644346003 scopus 로고    scopus 로고
    • note
    • 2O gave only the corresponding secondary alcohol from direct ring-opening.
  • 14
    • 4644270726 scopus 로고    scopus 로고
    • note
    • In the absence of LTMP, only secondary alcohols and chlorohydrins are observed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.