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Volumn 30, Issue 12, 2011, Pages 3284-3292

How racemic secondary alkyl electrophiles proceed to enantioselective products in Negishi cross-coupling reactions

Author keywords

[No Author keywords available]

Indexed keywords

CHIRALITY; ENANTIOMERS; ENANTIOSELECTIVITY; REACTION RATES;

EID: 84962438959     PISSN: 02767333     EISSN: 15206041     Source Type: Journal    
DOI: 10.1021/om1012049     Document Type: Article
Times cited : (56)

References (44)
  • 12
    • 23044496800 scopus 로고    scopus 로고
    • For asymmetric cross-coupling
    • For asymmetric cross-coupling: Arp, F. O.; Fu, G. C. J. Am. Chem. Soc. 2005, 127, 10482-10483
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 10482-10483
    • Arp, F.O.1    Fu, G.C.2
  • 16
    • 52449132069 scopus 로고    scopus 로고
    • 2) neucleophiles
    • 2) neucleophiles: Smith, S. W.; Fu, G. C. J. Am. Chem. Soc. 2008, 130, 12645-12647
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 12645-12647
    • Smith, S.W.1    Fu, G.C.2
  • 27
    • 77955908205 scopus 로고    scopus 로고
    • One step of oxidative addition and reductive elimination reported
    • One step of oxidative addition and reductive elimination reported: Wang, M.; Lin, Z. Organometallics 2010, 29, 3077-3084
    • (2010) Organometallics , vol.29 , pp. 3077-3084
    • Wang, M.1    Lin, Z.2
  • 36
    • 84962448151 scopus 로고    scopus 로고
    • note
    • As the solvent of DMA is not available in Gassuain 03, DMSO (dielectric constant ε = 47) was used to model DMA (ε =38).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.