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Volumn 7, Issue 13, 2005, Pages 2539-2541

Catalytic enantioselective Diels-Alder reaction via a chiral indium(III) complex

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EID: 23744514171     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol050518d     Document Type: Article
Times cited : (59)

References (58)
  • 1
    • 12344296858 scopus 로고    scopus 로고
    • Yamamoto, H., Ed.; Georg Thieme Verlag: Stuttgart
    • For reviews, see: (a) Loh, T.-P. In Science of Synthesis; Yamamoto, H., Ed.; Georg Thieme Verlag: Stuttgart, 2004; p 413.
    • (2004) Science of Synthesis , pp. 413
    • Loh, T.-P.1
  • 2
    • 26444501126 scopus 로고    scopus 로고
    • Activation of Reactions by Lewis acid derived from Ga, In, Sb and Bi
    • Atta-ur-Rahman, Ed. in press
    • (b) Loh, T.-P.; Chua, G.-L. Activation of Reactions by Lewis acid derived from Ga, In, Sb and Bi. Adv. Organic Synthesis - Online Atta-ur-Rahman, Ed. 2005, 1, in press.
    • (2005) Adv. Organic Synthesis - Online , vol.1
    • Loh, T.-P.1    Chua, G.-L.2
  • 31
    • 0000097153 scopus 로고    scopus 로고
    • Jacobson, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin
    • (b) Evans, D. A.; Johnson, J. S. In Comprehensive Asymmetric Catalysis; Jacobson, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999; Vol. 3, p 1177.
    • (1999) Comprehensive Asymmetric Catalysis , vol.3 , pp. 1177
    • Evans, D.A.1    Johnson, J.S.2
  • 36
    • 1842841091 scopus 로고    scopus 로고
    • For representative examples on catalytic enantioselective Diels-Alder reactions, see: (g) Ryu, D. H.; Zhou, G.; Corey, E. J. J. Am. Chem. Soc. 2004, 126, 4800.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 4800
    • Ryu, D.H.1    Zhou, G.2    Corey, E.J.3
  • 58
    • 29844438370 scopus 로고    scopus 로고
    • note
    • 4, filtered, and concentrated in vacuo. The residual crude product was purified via silica gel chromatography to afford the Diels-Alder adduct as a colorless solid (74% yield).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.