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Volumn 16, Issue 31, 2010, Pages 9453-9456

Erratum: Asymmetric synthesis of 4-amino-4H-chromenes by organocatalytic oxa-michael/aza-baylis-hillman tandem reactions (Chemistry - A European Journal (2010) 16 (9453-9456) DOI: 10.1002/chem.201001293);Asymmetric synthesis of 4-amino-4H-chromenes by organocatalytic oxa-Michael/aza-Baylis-Hillman tandem reactions

Author keywords

Asymmetric synthesis; Aza Baylis Hillman; Diarylprolinol ethers; Domino reactions; Organocatalysis; asymmetric synthesis; aza Baylis Hillman; diarylprolinol ethers; domino reactions; organocatalysis

Indexed keywords

CHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 77955827103     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201190221     Document Type: Erratum
Times cited : (80)

References (82)
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    • for the synthesis of racemic 4-amino-4H-chromenes, see: j) from allenes and tosylimines: Y.-L. Shi, M. Shi, Org. Lett. 2005, 7, 357;
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    • Some reports concerning to the racemic intermolecular versions of BH reaction activated triple bonds with hydride (reference [10h]), nitrogen (reference [10i]) and iodine (reference [10j]), all of them exhibiting an abnormal behaviour, have been reported
    • Some reports concerning to the racemic intermolecular versions of BH reaction activated triple bonds with hydride (reference [10h]), nitrogen (reference [10i]) and iodine (reference [10j]), all of them exhibiting an abnormal behaviour, have been reported.
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    • For a general review of the use of silyldiarylprolinol ethers as catalysts, see: a) A. Mielgo, C. Palomo, Chem. Asian J. 2008, 3, 922;
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    • For recent reviews on organocatalysis, see: a) P. I. Dalko, L. Moisan, Angew. Chem. 2004, 116, 5248;
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    • d) for a special volume on organocatalysis, see: Chem. Rev. 2007, 107;
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    • Note
    • 4 5%) in order to obtain product 4a, however we only detected starting material.
  • 81
    • 77955789137 scopus 로고    scopus 로고
    • CCDC-766985 (4' a) and 766986 (4a) contains the supplementary crystallographic data (see the Supporting Information for more details). These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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    • The allenamine intermediate II has been previously proposed by Wang et al, see reference [14b]
    • The allenamine intermediate II has been previously proposed by Wang et al, see reference [14b].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.