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Volumn , Issue 6, 2000, Pages 778-780

Synthesis of alkenylboronates via palladium-catalyzed borylation of alkenyl triflates (or Iodides) with pinacolborane

Author keywords

Boron; Cross coupling; Halides; Hydrides; Palladium; Triflates

Indexed keywords

BORON; BORONIC ACID DERIVATIVE; IODINE DERIVATIVE; TRIFLUOROMETHANESULFONIC ACID;

EID: 0034046120     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2000-6274     Document Type: Article
Times cited : (59)

References (29)
  • 15
    • 0342917770 scopus 로고    scopus 로고
    • note
    • The reaction of 2c with 1, followed by in situ treatment with an excess of trimethylamine oxide at 80 °C for 18 h, provided 4-tert-butylcyclohexanone in 457% yield together with 4-tert-butylcyclohex-2-en-1-ol (8%).
  • 16
    • 0003624033 scopus 로고
    • Academic: New York
    • For a review of the palladium-catalyzed carbon-carbon double bond isomerization, see; Heck, R. F. Palladium Reagents in Organic Synthesis; Academic: New York, 1985; p 19.
    • (1985) Palladium Reagents in Organic Synthesis , pp. 19
    • Heck, R.F.1
  • 24
    • 0343788689 scopus 로고    scopus 로고
    • note
    • The borylation of (E)-1 -iodo-3,3-dimethylbutene proceeded with retention of starting geometry to provide the corresponding (E)-alkenylboronate in 33% yield. Our synthetic study on the acyclic alkenyl system is as yet incomplete.
  • 26
    • 0343352942 scopus 로고    scopus 로고
    • note
    • To some extent, a plausible mechanism for the case of aryl halides proposed by us (see Ref. 4b) would refer to the present situation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.