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Volumn 14, Issue 10, 2012, Pages 2496-2499

Erratum : Correction to three-component organocascade kinetic resolution of racemic nitroallylic acetates via sequential iminium/enamine asymmetric catalysis (Org. Lett. (2012) 14 (10) (2496-2499) DOI: 10.1021/ol300783e);Three-component organocascade kinetic resolution of racemic nitroallylic acetates via sequential iminium/enamine asymmetric catalysis

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EID: 84862101306     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol503315p     Document Type: Erratum
Times cited : (31)

References (72)
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    • Wiley-VCH: Weinheim, For a recent review on organocatalysis, see
    • Dalko, P. I. Enantioselective Organoctalysis; Wiley-VCH: Weinheim, 2007. For a recent review on organocatalysis, see
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    • Dalko, P.I.1
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    • For the first example of organocascade kinetic resolution, see
    • For the first example of organocascade kinetic resolution, see: McGarraugh, P. G.; Brenner-Moyer, S. E. Org. Lett. 2011, 13, 6460
    • (2011) Org. Lett. , vol.13 , pp. 6460
    • McGarraugh, P.G.1    Brenner-Moyer, S.E.2
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    • 1H NMR analysis showing single proton signal as doublet at δ 6.96 with J = 2.0 Hz, due to the allylic coupling, see ref 6. Detailed X-ray crystallographic data for compound 3h (CCDC 869206) is available from the CCDC, 12 Union Road, Cambridge CB2 1EZ, U.K.
    • 1H NMR analysis showing single proton signal as doublet at δ 6.96 with J = 2.0 Hz, due to the allylic coupling, see ref 6. Detailed X-ray crystallographic data for compound 3h (CCDC 869206) is available from the CCDC, 12 Union Road, Cambridge CB2 1EZ, U.K. (www.ccdc.cam.ac. uk/data-request/cif).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.