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Volumn 21, Issue 30, 1980, Pages 2865-2868

The palladium-catalyzed cross-coupling reaction of 1-alkenylboranes with allylic or benzylic bromides. Convenient syntheses of 1,4-alkadienes and allybenzenes from alkynes via hydroboration

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EID: 0344117190     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)78629-1     Document Type: Article
Times cited : (103)

References (17)
  • 4
    • 84914373788 scopus 로고    scopus 로고
    • 2,3 were found to be not suitable for these reactions, because undesirable side reactions, allylation and benzylation of catechol occur competitively.
  • 5
    • 84914373787 scopus 로고    scopus 로고
    • In the reaction with 1-bromoethylbenzene, we obtained the homocoupling product, 2,3-diphenylbutane as the main product.
  • 7
    • 0003726028 scopus 로고
    • After the hydroboration of alkynes with disiamylborane, THF was evaporated at 15 mmHg for 2 h, and then the residue was dissolved in dry benzene. On the hydroboration of alkynes, see, John Wiley & Sons, New York
    • (1975) Organic Synthesis via Boranes
    • Brown1
  • 8
    • 84914373786 scopus 로고    scopus 로고
    • 7 of 1-phenyl-2-heptyne, and its retention time on GLC (capillary column, apiezon grease, 45 m) was longer than that of the E-isomer.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.