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Volumn 35, Issue 5, 1994, Pages 785-788

Elaboration of zirconacyclopentanes by sequential insertion of lithium chloroallylide and ketones or aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTANE DERIVATIVE;

EID: 0028118774     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)75817-5     Document Type: Article
Times cited : (36)

References (25)
  • 1
    • 0000759983 scopus 로고
    • Zirconocene-promoted stereoselective bicyclization of 1,6- and 1,7-dienes to produce trans-zirconabicyclo[3.3.0]octanes and cis-zirconabicyclo[4.3.0]nonanes
    • (1989) Tetrahedron Letters , vol.30 , pp. 5105
    • Rousset1    Swanson2    Lamaty3    Negishi4
  • 8
    • 84912982384 scopus 로고    scopus 로고
    • Kemp, M.; Whitby, R.J.; Coote, S.J. Synlett, in press
  • 11
    • 0010935879 scopus 로고
    • The reaction of thermally generated (ethylene)hafnocene with methylenetriphenylphosphorane: competing reaction paths leading to Cp2HfC2H5(CH:PPh3) and a hafnacyclobutane
    • The formation of a hafnacyclobutane in the reaction between (ethyle)nehafnocene and methylenetriphenylphosphorane may be viewed as a carbenoid ring expansion
    • (1985) Organometallics , vol.4 , pp. 2059
    • Erker1    Czisch2    Krüger3    Wallis4
  • 13
    • 0041802763 scopus 로고
    • Synthetic applications of metallate rearrangements
    • Also described as 1,2-metallate rearrangements this reaction type has found recent use in organic synthesis: review, These are also the basis of much boron chemistry - see ref 9 and therein
    • (1990) Pure and Applied Chemistry , vol.62 , pp. 1933
    • Kocienski1    Barber2
  • 15
    • 84913011361 scopus 로고    scopus 로고
    • 13C NMR, IR and Mass spectra including HRMS.
  • 16
    • 0001330838 scopus 로고
    • Organoboranes. 54. Exploration of the reactions of (.alpha.-haloallyl)lithium with organoborane derivatives. Simple and convenient procedure for the synthesis of three-carbon homologated boronate esters and terminal alkenes
    • In-situ lithiated allyl chloride has recently been used to homologate boron compounds and to ring expand boracyclanes
    • (1992) Organometallics , vol.11 , pp. 1948
    • Brown1    Rangaishenvi2    Jayaraman3
  • 20
    • 84913013629 scopus 로고    scopus 로고
    • 3-allyl complex by crystal structure determination: ref 10a.
  • 22
    • 0026565907 scopus 로고
    • Preparation and regio- and diastereoselective reactions of allylic zirconium reagents from allylic ether derivatives
    • (1992) Tetrahedron Letters , vol.33 , pp. 1295
    • Ito1    Taguchi2    Hanzawa3
  • 23
    • 84913007591 scopus 로고    scopus 로고
    • Bucker AC300, 75MHz, 32K FID zero-filled to 64K. The largest separation of diastereomer peaks was 0.07 p.p.m. The given ratios are the average from several pairs of signals using deconvolution to determine peak areas.
  • 24
    • 85077634689 scopus 로고
    • The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
    • (1981) Synthesis , pp. 1
    • Mitsonobu1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.