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Volumn 50, Issue 19, 2009, Pages 2256-2260

An expeditious synthesis of hexahydrobenzo[f]isochromenes and of hexahydrobenzo[f]isoquinoline via iodine-catalyzed Prins and aza-Prins cyclization

Author keywords

[No Author keywords available]

Indexed keywords

4 HYDROXY TETRAHYDROPYRAN; ALDEHYDE; BENZALDEHYDE; CHROMENE DERIVATIVE; HEXAHYDROBENZO[F]ISOCHROMENE DERIVATIVE; HEXAHYDROBENZO[F]ISOQUINOLINE; IODINE; ISOQUINOLINE DERIVATIVE; KETONE; SULFONAMIDE; TETRAHYDROPYRAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 62749141935     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.02.202     Document Type: Article
Times cited : (44)

References (55)
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  • 7
    • 35348836592 scopus 로고    scopus 로고
    • For reviews regarding Prins reaction and Prins cyclization, see:
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    • (2007) Curr. Org. Chem. , vol.11 , pp. 925
    • Pastor, I.M.1    Yus, M.2
  • 26
    • 44949148096 scopus 로고    scopus 로고
    • For recent reviews concerning iodine, see:
    • For recent reviews concerning iodine, see:. Stavber S., Jereb M., and Zupan M. Synthesis (2008) 1487
    • (2008) Synthesis , pp. 1487
    • Stavber, S.1    Jereb, M.2    Zupan, M.3
  • 31
    • 10044267850 scopus 로고    scopus 로고
    • For some reactions using iodine as Lewis acid, see:
    • For some reactions using iodine as Lewis acid, see:. Sun J., Dong Y., Cao L., Wang X., Wang S., and Hu Y. J. Org. Chem. 69 (2004) 8932
    • (2004) J. Org. Chem. , vol.69 , pp. 8932
    • Sun, J.1    Dong, Y.2    Cao, L.3    Wang, X.4    Wang, S.5    Hu, Y.6
  • 47
    • 0027956693 scopus 로고
    • Terminal olefins and endocyclic olefins afforded 4-exo-tet iodocyclization products:
    • Terminal olefins and endocyclic olefins afforded 4-exo-tet iodocyclization products:. Galatsis P., and Parks D.J. Tetrahedron Lett. 35 (1994) 6611
    • (1994) Tetrahedron Lett. , vol.35 , pp. 6611
    • Galatsis, P.1    Parks, D.J.2
  • 54
    • 33644696397 scopus 로고    scopus 로고
    • The relative configuration of 23 and 24 was assigned by comparison to the NMR data of other 4-hydroxy-tetrahydropyrans.
    • The relative configuration of 23 and 24 was assigned by comparison to the NMR data of other 4-hydroxy-tetrahydropyrans. Abate A., Allievi M., Brenna E., Fuganti C., Gatti F.G., and Serra S. Helv. Chim. Acta 89 (2006) 177
    • (2006) Helv. Chim. Acta , vol.89 , pp. 177
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.