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Volumn 30, Issue 1, 2009, Pages 33-34

Decarboxylative protonation of allyl ester catalyzed by Pt and Ru

Author keywords

Decarboxylative protonation; Grubbs catalyst; Platinum

Indexed keywords


EID: 60149107184     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2009.30.1.033     Document Type: Article
Times cited : (3)

References (28)
  • 1
    • 0001699424 scopus 로고
    • For Tsuji's contribution on Pd-assisted decarboxylative protonation and allylation, see
    • For Tsuji's contribution on Pd-assisted decarboxylative protonation and allylation, see: Tsuji, J.; Nisar, M.; Shimizu, I. J. Org. Chem. 1985, 50, 3416-3417.
    • (1985) J. Org. Chem. , vol.50 , pp. 3416-3417
    • Tsuji, J.1    Nisar, M.2    Shimizu, I.3
  • 4
    • 45549100093 scopus 로고    scopus 로고
    • For the other contributions on Pd-assisted decarboxylative protonation, see
    • For the other contributions on Pd-assisted decarboxylative protonation, see: Marinescu, S. C.; Nishimata, T.; Mohr, J. T.; Stoltz, B. M. Org. Lett., 2008, 10, 1039-1042.
    • (2008) Org. Lett. , vol.10 , pp. 1039-1042
    • Marinescu, S.C.1    Nishimata, T.2    Mohr, J.T.3    Stoltz, B.M.4
  • 7
    • 0033591414 scopus 로고    scopus 로고
    • For some examples on the formation of π-allylmetal complex and their synthetic applications, see
    • For some examples on the formation of π-allylmetal complex and their synthetic applications, see: Blacker, A. J.; Clarke, M. L.; Loft, M. S.; Williams, J. M. J. Chem. Commun., 1999, 913-914.
    • (1999) Chem. Commun. , pp. 913-914
    • Blacker, A.J.1    Clarke, M.L.2    Loft, M.S.3    Williams, J.M.J.4
  • 17
    • 18744415432 scopus 로고    scopus 로고
    • and further references cited therein
    • Tunge, J. A.; Burger, E. C. Eur. J. Org. Chem. 2005, 1715-1726 and further references cited therein.
    • (2005) Eur. J. Org. Chem. , pp. 1715-1726
    • Tunge, J.A.1    Burger, E.C.2
  • 18
    • 60149088767 scopus 로고    scopus 로고
    • note
    • 2 without TPP.
  • 25
    • 60149112556 scopus 로고    scopus 로고
    • note
    • 3 Other compounds were synthesized similarly and the representative spectroscopic data of 1b, 1c, and 3c are as follows.
  • 26
    • 60149110115 scopus 로고    scopus 로고
    • note
    • 3, 75 MHz) δ 14.07, 30.34, 33.29, 51.20, 61.43, 65.85, 118.58, 126.20, 128.45, 128.52, 131.59, 140.57, 169.00, 169.16.
  • 27
    • 60149097803 scopus 로고    scopus 로고
    • note
    • 3, 75 MHz) δ 29.58, 33.89, 61.10, 65.86, 118.78, 126.60, 128.48, 128.68, 131.29, 137.93, 168.64, 202.13.
  • 28
    • 60149085969 scopus 로고    scopus 로고
    • note
    • 3, 75 MHz) δ 30.48, 35.65, 37.32, 54.14, 117.20, 126.30, 128.45, 128.84, 135.09, 139.37, 211.45.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.