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Volumn 5, Issue 8, 2013, Pages 2360-2366

Easily-controlled chemoselective hydrogenation by using palladium on boron nitride

Author keywords

Boron; Chemoselectivity; Heterogeneous catalysis; Hydrogenation; Palladium

Indexed keywords

ARYL HALIDES; ARYL KETONES; BENZYL ETHERS; CHEMO-SELECTIVITY; CHEMOSELECTIVE; CHEMOSELECTIVE HYDROGENATION; DIETHYLENETRIAMINE; SEMIHYDROGENATION;

EID: 84880941124     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.201300035     Document Type: Article
Times cited : (36)

References (68)
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    • Hudlicky, M.1
  • 9
    • 84880944384 scopus 로고    scopus 로고
    • For selected papers on chemoselective hydrogenation using transition metals other than supported Pd heterogeneous catalysts, see:
    • For selected papers on chemoselective hydrogenation using transition metals other than supported Pd heterogeneous catalysts, see:
  • 31
    • 84880961812 scopus 로고    scopus 로고
    • We have reported the Pd/MS3A-catalyzed chemoselective hydrogenation of azide, alkyne, and alkene functionalities in the presence of other reducible groups. See Ref.[11].
    • We have reported the Pd/MS3A-catalyzed chemoselective hydrogenation of azide, alkyne, and alkene functionalities in the presence of other reducible groups. See Ref.[11].
  • 32
    • 84880959214 scopus 로고    scopus 로고
    • For semihydrogenations, see:
    • For semihydrogenations, see:
  • 50
    • 84880928540 scopus 로고    scopus 로고
    • 2 for the deactivation of the catalyst and the difficulty of the semihydrogenation for monosubstituted alkynes. See Ref.[8].
    • 2 for the deactivation of the catalyst and the difficulty of the semihydrogenation for monosubstituted alkynes. See Ref.[8].
  • 51
    • 84880927451 scopus 로고    scopus 로고
    • Although Pd/PEI enabled the semihydrogenation of both mono- and disubstituted alkynes, the careful adjustment of the reaction conditions, such as the solvent, was required for each substrate. Furthermore, the reuse of the catalyst was not possible. See Ref.[8].
    • Although Pd/PEI enabled the semihydrogenation of both mono- and disubstituted alkynes, the careful adjustment of the reaction conditions, such as the solvent, was required for each substrate. Furthermore, the reuse of the catalyst was not possible. See Ref.[8].
  • 54
    • 84880939893 scopus 로고    scopus 로고
    • A small amount of Pd metal (2.2%) was leached during the semihydrogenation catalyzed by Pd/BN-DETA in MeOH. Therefore, the leaching of Pd might be slightly promoted by the addition of DETA. See Ref.[17a].
    • A small amount of Pd metal (2.2%) was leached during the semihydrogenation catalyzed by Pd/BN-DETA in MeOH. Therefore, the leaching of Pd might be slightly promoted by the addition of DETA. See Ref.[17a].
  • 55
    • 84880941271 scopus 로고    scopus 로고
    • 2-Pd/BN-MeOH).
    • 2-Pd/BN-MeOH).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.