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Volumn 23, Issue 6, 2012, Pages 925-929

Synthesis of 2-aryl-substituted chromans by intramolecular C-O bond formation

Author keywords

chalcones; chromans; copper; intramolecular cyclization; palladium

Indexed keywords

2 (2 BROMOPHENYL)CHROMAN; 2 (2 PIPERIDYL)CHROMAN; 2 (2 PYRROLIDYL)CHROMAN; 2 [(1,1' BIPHENYL) 2 ARYL]CHROMAN; 2 ALKYL CHROMAN; 2 ARYL SUBSTITUTED CHROMAN DERIVATIVE; 2 BROMOALDEHYDE; 2 BROMOPHENYLPROPANOL DERIVATIVE; 2 FURYLCHROMAN; 2 HETEROARYL SUBSTITUTED CHROMAN DERIVATIVE; 2 PHENYL CHROMAN; 3 (2 BROMOPHENYL)PROPAN 1 OL DERIVATIVE; 4',6 DICHLOROFLAVAN; ALCOHOL DERIVATIVE; ALDEHYDE DERIVATIVE; ALPHA TOCOPHEROL; ARYLBROMIDE DERIVATIVE; BENZENEBORONIC ACID; BROMINE DERIVATIVE; CHALCONE DERIVATIVE; CHROMAN DERIVATIVE; COPPER; INDOLE PHOSPHINE OXAZOLINE; KETONE; METHYL SUBSTITUTED ARYL PROPANOL DERIVATIVE; OXAZOLINE DERIVATIVE; OXIME; PALLADIUM; PHENYL SUBSTITUTED ARYL PROPANOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84862777735     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1290607     Document Type: Article
Times cited : (16)

References (40)
  • 13
    • 64349094226 scopus 로고    scopus 로고
    • For a recent review on the asymmetric synthesis of chromans, see:, Shen H C., Tetrahedron 2009 65 3931
    • (2009) Tetrahedron , vol.65 , pp. 3931
    • Shen, H.C.1
  • 26
    • 84862796484 scopus 로고    scopus 로고
    • The by-product was 1-(furan-2-yl)-3-phenylpropan-1-one, isolated in 22% yield. For the reaction mechanism, see reference 7b.
    • The by-product was 1-(furan-2-yl)-3-phenylpropan-1-one, isolated in 22% yield. For the reaction mechanism, see reference 7b.
  • 31
    • 84862831863 scopus 로고    scopus 로고
    • The reported ee is the average value of three entries.
    • The reported ee is the average value of three entries.
  • 32
    • 84862796483 scopus 로고    scopus 로고
    • 2, 87% ee)
    • 2, 87% ee).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.