메뉴 건너뛰기




Volumn 53, Issue 21, 2014, Pages 5458-5461

Organocatalytic atroposelective aldol condensation: Synthesis of axially chiral biaryls by arene formation

Author keywords

aldol reaction; atropisomerism; enantioselectivity; organocatalysis; polyketides

Indexed keywords

AROMATIC COMPOUNDS; AROMATIZATION; BIOCHEMISTRY; BIOSYNTHESIS; CATALYSTS; CHIRALITY; CONDENSATION REACTIONS; ENANTIOSELECTIVITY; KETONES; REACTION KINETICS;

EID: 84900843512     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201402441     Document Type: Article
Times cited : (153)

References (52)
  • 2
    • 69249202590 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 4688-4716
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 4688-4716
  • 19
    • 54649084880 scopus 로고    scopus 로고
    • for asymmetric organocatalytic domino reactions, see
    • Angew. Chem. Int. Ed. 2008, 47, 7656-7658; for asymmetric organocatalytic domino reactions, see
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 7656-7658
  • 21
    • 33947198541 scopus 로고    scopus 로고
    • for asymmetric dienamine activation, see
    • Angew. Chem. Int. Ed. 2007, 46, 1570-1581; for asymmetric dienamine activation, see
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1570-1581
  • 31
    • 24644462889 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 5384-5427
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 5384-5427
  • 33
    • 70349894963 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 6398-6401
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6398-6401
  • 36
  • 39
    • 0033579641 scopus 로고    scopus 로고
    • a Ferrier-type rearrangement via an enolate anion with a chiral guanidinium counterion to a biaryl with 12 % ee was recently reported
    • T. Bach, J. Schröder, K. Harms, Tetrahedron Lett. 1999, 40, 9003-9004; a Ferrier-type rearrangement via an enolate anion with a chiral guanidinium counterion to a biaryl with 12 % ee was recently reported
    • (1999) Tetrahedron Lett. , vol.40 , pp. 9003-9004
    • Bach, T.1    Schröder, J.2    Harms, K.3
  • 42
    • 4544311534 scopus 로고    scopus 로고
    • aryne formation from ortho-bromophenylmagnesiumchloriḋLiCl could be sufficiently prevented by cooling the reaction mixture to -15 C
    • Angew. Chem. Int. Ed. 2004, 43, 3333-3336: aryne formation from ortho-bromophenylmagnesiumchloriḋLiCl could be sufficiently prevented by cooling the reaction mixture to -15 C.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 3333-3336
  • 45
    • 33751158088 scopus 로고
    • The addition of water significantly accelerates the Dess-Martin- oxidation:, The reaction was monitored by NMR spectroscopy
    • The addition of water significantly accelerates the Dess-Martin- oxidation:, S. D. Meyer, S. L. Schreiber, J. Org. Chem. 1994, 59, 7549-7552. The reaction was monitored by NMR spectroscopy.
    • (1994) J. Org. Chem. , vol.59 , pp. 7549-7552
    • Meyer, S.D.1    Schreiber, S.L.2
  • 50


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.