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Volumn 68, Issue 17, 2012, Pages 3435-3443

Copper catalyzed tandem conjugated borylation-aldol reaction

Author keywords

Aldol reaction; Boron; Catalysis; Copper; Domino reaction

Indexed keywords

3 CYCLOHEXYL 3 HYDROXY 2 (HYDROXYMETHYL) N METHOXY N METHYLPROPANAMIDE; 3 CYCLOHEXYL 3 HYDROXY 2 (HYDROXYMETHYL)PROPANENITRILE; 3 HYDROXY 2 (2 HYDROXYMETHYL) 3 PHENYLPROPANENITRILE; 3 HYDROXY 2 (HYDROXYMETHYL) N METHOXY 3 (4 METHOXY PHENYL) N METHYLPROPANAMIDE; 3 HYDROXY 2 (HYDROXYMETHYL) N METHOXY N METHYL 3 (THIOPHEN 2 YL)PROPANAMIDE; 3 HYDROXY 2 (HYDROXYMETHYL) N METHOXY N METHYL 3 PHENYLPROPANAMIDE; 4 CYCLOHEXYL 4 HYDROXY 3 (HYDROXYMETHYL)BUTAN 2 ONE; 4 HYDROXY 3 (HYDROXYMETHYL) 4 PHENYLBUTAN 2 ONE; ALKYNE; CARBON; COPPER; ETHYL 3 CYCLOHEXYL 3 HYDROXY 2 (HYDROXYMETHYL) 2 METHYLPROPANOATE; METHYL 3 (4 CHLOROPHENYL) 3 HYDROXY 2 (HYDROXYMETHYL)PROPANOATE; METHYL 3 (FURAN 2 YL) 3 HYDROXY 2 (HYDROXYMETHYL)PROPANOATE; METHYL 3 CYCLOHEXYL 3 HYDROXY 2 (HYDROXYMETHYL)PROPANOATE; METHYL 3 HYDROXY 2 (1 HYDROXYCYCLOHEXYL)PROPANOATE; METHYL 3 HYDROXY 2 (HYDROXYMETHYL) 2 METHYL 3 PHENYLPROPANOATE; METHYL 3 HYDROXY 2 (HYDROXYMETHYL) 3 (4 METHOXYPHENYL)PROPANOATE; METHYL 3 HYDROXY 2 (HYDROXYMETHYL) 3 [4 (TRIFLUOROMETHYL)PHENYL]PROPANOATE; METHYL 3 HYDROXY 2 (HYDROXYMETHYL) 3 PHENYLBUTANOATE; METHYL 3 HYDROXY 2 (HYDROXYMETHYL) 3 PHENYLPROPANOATE; METHYL 3 HYDROXY 2 (HYDROXYMETHYL) 4,4 DIMETHYLPENTANOATE; METHYL 3 HYDROXY 2 (HYDROXYMETHYL) 5 PHENYLPENTANOATE; UNCLASSIFIED DRUG;

EID: 84859543225     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2011.07.062     Document Type: Conference Paper
Times cited : (30)

References (65)
  • 14
    • 84555174469 scopus 로고    scopus 로고
    • Copper (I) hydride reagents and catalysts
    • Z. Rappoport, I. Marek, John Wiley & Sons Ltd Chichester, UK
    • O. Riant Copper (I) hydride reagents and catalysts Z. Rappoport, I. Marek, The Chemistry of Organocopper Compounds 2009 John Wiley & Sons Ltd Chichester, UK 731 774
    • (2009) The Chemistry of Organocopper Compounds , pp. 731-774
    • Riant, O.1
  • 38
    • 77949410450 scopus 로고    scopus 로고
    • Other examples of tandem borosilylation-tandem reaction
    • Other examples of tandem borosilylation-tandem reaction: K.-s. Lee, and A.H. Hoveyda J. Am. Chem. Soc. 132 2010 2898 2900
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 2898-2900
    • Hoveyda, A.H.1
  • 44
    • 76349094490 scopus 로고    scopus 로고
    • Review on enantioselective conjugated borylation and references herein:, For recent developments
    • Review on enantioselective conjugated borylation and references herein: J.A. Schiffner, K. Müther, and M. Oestreich Angew. Chem., Int. Ed. 49 2010 1194 1196 For recent developments
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 1194-1196
    • Schiffner, J.A.1    Müther, K.2    Oestreich, M.3
  • 53
    • 0000493922 scopus 로고
    • 3·2MeOH was prepared according to a literature procedure
    • 3·2MeOH was prepared according to a literature procedure: D.J. Gulliver, W. Levason, and M. Webster Inorg. Chim. Acta 52 1981 153 159
    • (1981) Inorg. Chim. Acta , vol.52 , pp. 153-159
    • Gulliver, D.J.1    Levason, W.2    Webster, M.3
  • 56
    • 0037011208 scopus 로고    scopus 로고
    • For a related copper(I) catalysed reductive aldol reaction with boron hydride reagents and boron enolate intermediates, see
    • For a related copper(I) catalysed reductive aldol reaction with boron hydride reagents and boron enolate intermediates, see: P. Papa, and B.H. Lipshutz Angew. Chem., Int. Ed. 41 2002 4580 4582
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 4580-4582
    • Papa, P.1    Lipshutz, B.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.