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Volumn , Issue 19, 2011, Pages 3152-3160

Waste-free catalytic propargylation/allenylation of aryl and heteroaryl nucleophiles and synthesis of naphthopyrans

Author keywords

boronic acids; Friedel Crafts reaction; organocatalysis; propargylic alcohols

Indexed keywords

2-NAPHTHOLS; ARYLBORONIC ACIDS; BORONIC ACID; CARBOCATIONS; CARBOCYCLES; ELECTRON-RICH AROMATICS; ENVIRONMENTALLY BENIGN; FRIEDEL-CRAFTS; GENERAL METHOD; HETEROCYCLES; HIGH YIELD; IN-SITU; NAPHTHOPYRANS; ORGANOCATALYSIS; PRODUCING WATER; PROPARGYL; PROPARGYLATION; PROPARGYLIC ALCOHOLS; SUBSTITUTION MECHANISMS;

EID: 80053050941     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1260146     Document Type: Article
Times cited : (43)

References (66)
  • 25
    • 64149095592 scopus 로고    scopus 로고
    • For an excellent review on the direct arylation of -activated alcohols, see:, Bandini M, Tragni M, Org. Biomol. Chem. 2009 7 1501
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 1501
    • Bandini, M.1    Tragni, M.2
  • 26
    • 58949090614 scopus 로고    scopus 로고
    • Allenyl substitution products have recently been reported with allylic nucleophiles:, Lee K, Lee P H., Org. Lett. 2008 10 2441
    • (2008) Org. Lett. , vol.10 , pp. 2441
    • Lee, K.1    Lee, P.H.2
  • 47
    • 65249099565 scopus 로고    scopus 로고
    • 3 has been successfully employed in substitution reactions of related alcohols with cyanide and alcohol nucleophiles:, Rajagopal G, Kim S S., Tetrahedron 2009 65 4351
    • (2009) Tetrahedron , vol.65 , pp. 4351
    • Rajagopal, G.1    Kim, S.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.