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Volumn 76, Issue 2, 2008, Pages 1285-1300

Asymmetric hetero diels-alder reaction of nitroso compounds utilizing tartaric acid ester as a chiral auxiliary

Author keywords

Cyclohexa 1,3 dienylmethanol; Dihydro 1,2 oxazine; Enantioselective; Zinc Alkoxide

Indexed keywords


EID: 61349098930     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-08-S(N)94     Document Type: Article
Times cited : (11)

References (24)
  • 13
    • 0030182907 scopus 로고    scopus 로고
    • Although an enantioselective hetero Diels-Alder reaction of a nitroso compound promoted by an antibody was reported, the enantioselectivity was not sufficient;
    • Although an enantioselective hetero Diels-Alder reaction of a nitroso compound promoted by an antibody was reported, the enantioselectivity was not sufficient;. Meekel A.A.P., Resmini M., and Pandit U.K. Bioorg. Med. Chem. 4 (1996) 1051
    • (1996) Bioorg. Med. Chem. , vol.4 , pp. 1051
    • Meekel, A.A.P.1    Resmini, M.2    Pandit, U.K.3
  • 14
    • 33846781519 scopus 로고    scopus 로고
    • Related nitroso Diels-Alder-type ring formation
    • Related nitroso Diels-Alder-type ring formation. Momiyama N., Yamamoto Y., and Yamamoto H. J. Am. Chem. Soc. 129 (2007) 1190
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 1190
    • Momiyama, N.1    Yamamoto, Y.2    Yamamoto, H.3
  • 15
    • 34547610208 scopus 로고    scopus 로고
    • A sequential method to access chiral 1,2-oxazines by an asymmetric α-oxyamination of carbonyl compounds and conjugate addition to vinylphosphonium salts, followed by an intramolecular Wittig reaction was reported:
    • A sequential method to access chiral 1,2-oxazines by an asymmetric α-oxyamination of carbonyl compounds and conjugate addition to vinylphosphonium salts, followed by an intramolecular Wittig reaction was reported:. Kumarn S., Oelke A.J., Shaw D.M., Longbottom D.A., and Ley S.V. Org. Biomol. Chem. 5 (2007) 2678
    • (2007) Org. Biomol. Chem. , vol.5 , pp. 2678
    • Kumarn, S.1    Oelke, A.J.2    Shaw, D.M.3    Longbottom, D.A.4    Ley, S.V.5
  • 19
    • 33745400676 scopus 로고    scopus 로고
    • A similar strategy was already found to be effective for an asymmetric Diels-Alder reaction of o-quinodimethanes:
    • A similar strategy was already found to be effective for an asymmetric Diels-Alder reaction of o-quinodimethanes:. Takinami M., Ukaji Y., and Inomata K. Tetrahedron: Asymmetry 17 (2006) 1554
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 1554
    • Takinami, M.1    Ukaji, Y.2    Inomata, K.3
  • 21
    • 61349118367 scopus 로고    scopus 로고
    • 11 was incorrect and should be corrected as described in this manuscript.
    • 11 was incorrect and should be corrected as described in this manuscript.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.