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Volumn 54, Issue 9, 2015, Pages 2780-2783

Fine-tuning the nucleophilic reactivities of boron ate complexes derived from aryl and heteroaryl boronic esters

Author keywords

Arenes; Boron compounds; Kinetics; Linear free energy relationships; Nucleophilicity

Indexed keywords

BORON; BORON COMPOUNDS; CRYSTALLOGRAPHY; ENZYME KINETICS; ESTERIFICATION; ESTERS; ETHYLENE; ETHYLENE GLYCOL; FREE ENERGY; IONS; PHENOLS; POLYOLS; SUBSTITUTION REACTIONS; ULTRAVIOLET VISIBLE SPECTROSCOPY;

EID: 85027939203     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201410562     Document Type: Article
Times cited : (26)

References (33)
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    • 84923103174 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 11172-11176.
    • (2014) Angew. Chem. , vol.126 , pp. 11172-11176
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    • 85028144510 scopus 로고    scopus 로고
    • Angew. Chem. 2014, DOI: 10.1002/ange.201407701.
    • (2014) Angew. Chem.
  • 19
    • 85028150145 scopus 로고    scopus 로고
    • http://www.cup.lmu.de/oc/mayr/DBintro.html.
  • 20
    • 85028156373 scopus 로고    scopus 로고
    • note
    • The trifluoromethylated BACs 3 and 4 can be kept for a few minutes in aqueous acetonitrile but then they decompose quantitatively into 2-methylthiophene and the corresponding aryl boronic esters.
  • 21
    • 85028138576 scopus 로고    scopus 로고
    • Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 28
    • 85028147300 scopus 로고    scopus 로고
    • note
    • +, see the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.