메뉴 건너뛰기




Volumn 13, Issue 36, 2007, Pages 10246-10256

Highly diastereo- and enantioselective direct aldol reactions of aldehydes and ketones catalyzed by siloxyproline in the presence of water

Author keywords

Aldol reaction; Asymmetric synthesis; Organocatalysis; Proline; Sustainable chemistry; Water

Indexed keywords

CATALYST ACTIVITY; ENANTIOSELECTIVITY; KETONES; ORGANIC SOLVENTS; SYNTHESIS (CHEMICAL);

EID: 38049151296     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200700363     Document Type: Article
Times cited : (170)

References (131)
  • 4
    • 38049132041 scopus 로고    scopus 로고
    • Ed, U. M. Lindstrom, Blackwell Publishing, Oxford
    • d) Organic Reactions in Water. (Ed.: U. M. Lindstrom), Blackwell Publishing, Oxford, 2007.
    • (2007) Reactions in Water
    • Organic1
  • 8
    • 20344388819 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 3275-3279.
    • (2005) Chem. Int. Ed , vol.44 , pp. 3275-3279
    • Angew1
  • 9
    • 0003445429 scopus 로고    scopus 로고
    • Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin
    • Comprehensive Asymmetric Catalysis I-III, (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin, 1999.
    • (1999) Comprehensive Asymmetric Catalysis I-III
  • 13
    • 33845963606 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 63, 5138-5175;
    • (2004) Chem. Int. Ed , vol.63 , pp. 5138-5175
    • Angew1
  • 19
    • 55049138759 scopus 로고    scopus 로고
    • Ed, P. I. Dalko, Wiley-VCH, Weinheim
    • h) Enantioselective Organocatalysis, (Ed.: P. I. Dalko), Wiley-VCH, Weinheim, 2007.
    • (2007) Enantioselective Organocatalysis
  • 20
    • 33847093544 scopus 로고    scopus 로고
    • For a review, see:, Ed, R. Mahrwald, Wiley-VCH, Weinheim
    • For a review, see: Modem Aldol Reactions, vols. 1 and 2 (Ed.: R. Mahrwald), Wiley-VCH, Weinheim, 2004.
    • (2004) Modem Aldol Reactions, vols. 1 and 2
  • 22
    • 0034678591 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 1352-1375:
    • (2000) Chem. Int. Ed , vol.39 , pp. 1352-1375
    • Angew1
  • 35
    • 24044485355 scopus 로고    scopus 로고
    • For a review. see:, Ed, R. Mahrwald, Wiley-VCH, Weinheim, Chapter 6, pp
    • k) For a review. see:M. Shibasaki, S. Matsunaga, N. Kumagai, in Modem Aldol Reactions, vol. 2 (Ed.: R. Mahrwald), Wiley-VCH, Weinheim, 2004, Chapter 6, pp. 197-227.
    • (2004) Modem Aldol Reactions , vol.2 , pp. 197-227
    • Shibasaki, M.1    Matsunaga, S.2    Kumagai, N.3
  • 42
    • 0042819676 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 3927-3930;
    • (2003) Chem. Int. Ed , vol.42 , pp. 3927-3930
    • Angew1
  • 48
    • 22944480542 scopus 로고    scopus 로고
    • H.-J. Li, H.-Y. Tian, Y.-C. Wu,l Y.-J. Chen, L. Liu, D. Wang, C.-J. Li. Adv. Synth. Catal. 2005, 347, 1247-1256;
    • l) H.-J. Li, H.-Y. Tian, Y.-C. Wu,l Y.-J. Chen, L. Liu, D. Wang, C.-J. Li. Adv. Synth. Catal. 2005, 347, 1247-1256;
  • 59
    • 13644256524 scopus 로고    scopus 로고
    • Amine-Catalyzed Aldol Reactions
    • For reviews, see: a, Ed, R. Mahrwald, Wiley-VCH. Weinheim, Chapter 4;
    • For reviews, see: a) B. List. Amine-Catalyzed Aldol Reactions, in Modern Aldol Reactions, vol. I (Ed.: R. Mahrwald). Wiley-VCH. Weinheim. 2004, Chapter 4;
    • (2004) Modern Aldol Reactions , vol.1
    • List, B.1
  • 60
    • 0037043180 scopus 로고    scopus 로고
    • b) B. List. Tetrahedron 2002, 58, 5573-5590;
    • (2002) Tetrahedron , vol.58 , pp. 5573-5590
    • List, B.1
  • 68
    • 33750460594 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 6924-6926;
    • (2006) Chem. Int. Ed , vol.45 , pp. 6924-6926
    • Angew1
  • 71
    • 5144234219 scopus 로고    scopus 로고
    • For organocatalysis-mediated asymmetric aldol reactions in aqueous solvents, see: a
    • For organocatalysis-mediated asymmetric aldol reactions in aqueous solvents, see: a) H. Torii, M. Nakadai, K. Ishihara, S. Saito, H. Yamamoto, Angew. Chem. 2004, 116, 2017-2020;
    • (2004) Angew. Chem , vol.116 , pp. 2017-2020
    • Torii, H.1    Nakadai, M.2    Ishihara, K.3    Saito, S.4    Yamamoto, H.5
  • 72
    • 2942641357 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 1983-1986;
    • (2004) Chem. Int. Ed , vol.43 , pp. 1983-1986
    • Angew1
  • 90
    • 32044463187 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 958-961.
    • (2006) Chem. Int. Ed , vol.45 , pp. 958-961
    • Angew1
  • 93
    • 33748655418 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 5527-5529.
    • (2006) Chem. Int. Ed , vol.45 , pp. 5527-5529
    • Angew1
  • 101
    • 33845728625 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 8100-8102.
    • (2006) Chem. Int. Ed , vol.45 , pp. 8100-8102
    • Angew1
  • 102
  • 103
    • 33845788846 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 8103-8104.
    • (2006) Chem. Int. Ed , vol.45 , pp. 8103-8104
    • Angew1
  • 115
    • 14844316261 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 1369-1371;
    • (2005) Chem. Int. Ed , vol.44 , pp. 1369-1371
    • Angew1
  • 124
    • 15444380834 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 1210-1212;
    • (2005) Chem. Int. Ed , vol.44 , pp. 1210-1212
    • Angew1
  • 127
    • 0003601534 scopus 로고    scopus 로고
    • 12th edition, Merck and Co, Inc, p
    • N. J. Rahway, in The Merck Index, 12th edition, Merck and Co., Inc., p. 2795.
    • The Merck Index , pp. 2795
    • Rahway, N.J.1
  • 128
    • 0003601534 scopus 로고    scopus 로고
    • 12th edition, Merck and Co, Inc, p
    • N. J. Rahway, in The Merck Index, 12th edition, Merck and Co., Inc., p. 1089.
    • The Merck Index , pp. 1089
    • Rahway, N.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.