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Volumn 55, Issue 2, 2003, Pages 87-99

The L-Proline-Catalyzed Asymmetric Syntheses

Author keywords

Asymmetric syntheses; L Proline

Indexed keywords

ALCOHOLS; MOLECULAR DYNAMICS; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 0142215694     PISSN: 10161015     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (3)

References (18)
  • 1
    • 0035793248 scopus 로고    scopus 로고
    • The Application of L-Proline as an Enzyme Mimic and Futher New Asymmetric Syntheses Using Small Organic Molecules as Chiral Catalysts
    • Gröger, H.; Wilken, J. The Application of L-Proline as an Enzyme Mimic and Futher New Asymmetric Syntheses Using Small Organic Molecules as Chiral Catalysts. Angew. Chem. Int. Ed. 2001, 40, 529-532.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 529-532
    • Gröger, H.1    Wilken, J.2
  • 2
    • 84981886574 scopus 로고
    • New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures
    • Eder, U.; Sauer, G.; Wiechert, R. New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial Structures. Angew. Chem. Int. Ed. 1971, 10, 496-497.
    • (1971) Angew. Chem. Int. Ed. , vol.10 , pp. 496-497
    • Eder, U.1    Sauer, G.2    Wiechert, R.3
  • 3
    • 33847804003 scopus 로고
    • Asymetric Synthesis of Bicyclic Intermediates of Natural Product Chemistry
    • Hajos, Z. G.; Parrish, D. R. Asymetric Synthesis of Bicyclic Intermediates of Natural Product Chemistry. J. Org. Chem. 1974, 39, 1615-1621.
    • (1974) J. Org. Chem. , vol.39 , pp. 1615-1621
    • Hajos, Z.G.1    Parrish, D.R.2
  • 4
    • 0037425534 scopus 로고    scopus 로고
    • Kinetic and Stereochemical Evidence for the Involvement of only One Proline Molecule in the Transition States of Proline-Catalyzed Intra- and Intermolecular Aldol Reactions
    • Hoang, L.; Bahmanyar, S.; Houk, K. N.; List, B. Kinetic and Stereochemical Evidence for the Involvement of only One Proline Molecule in the Transition States of Proline-Catalyzed Intra- and Intermolecular Aldol Reactions. J. Am. Chem. Soc. 2003, 125, 16-17.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 16-17
    • Hoang, L.1    Bahmanyar, S.2    Houk, K.N.3    List, B.4
  • 5
    • 0001332919 scopus 로고
    • Is the Mechanism of the Proline-catalyzed Enantio-selective Aldol Reaction Related to Biochemical Processes?
    • Agami, C.; Puchot, C.; Sevestre, H. Is the Mechanism of the Proline-catalyzed Enantio-selective Aldol Reaction Related to Biochemical Processes? Tetrahedron Lett. 1986, 27, 1501-1504.
    • (1986) Tetrahedron Lett. , vol.27 , pp. 1501-1504
    • Agami, C.1    Puchot, C.2    Sevestre, H.3
  • 6
    • 33845374428 scopus 로고
    • Nonlinear Effects in Asymmetric Synthesis. Examples in Asymmetric Oxidations and Aldolization Reactions
    • Puchot, C.; Samuel, O.; Dunach, E.; Zhao, S.; Agami, C.; Kagan, H. B. Nonlinear Effects in Asymmetric Synthesis. Examples in Asymmetric Oxidations and Aldolization Reactions. J. Am. Chem. Soc. 1986, 108, 2353-2357.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 2353-2357
    • Puchot, C.1    Samuel, O.2    Dunach, E.3    Zhao, S.4    Agami, C.5    Kagan, H.B.6
  • 7
    • 0034812506 scopus 로고    scopus 로고
    • Amino Acid Catalyzed Direct Asymmetric Aldol Reactions A Bioorganic Approach to Catalytic Asymmetric Carbon-Forming Reactions
    • Sakthivel, K.; Notz, W.; Bui, T.; Barbas III, C. F. Amino Acid Catalyzed Direct Asymmetric Aldol Reactions: A Bioorganic Approach to Catalytic Asymmetric Carbon-Forming Reactions. J. Am. Chem. Soc. 2001, 123, 5260-5267.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 5260-5267
    • Sakthivel, K.1    Notz, W.2    Bui, T.3    Barbas C.F. III4
  • 8
    • 0034654216 scopus 로고    scopus 로고
    • Proline-Catalyzed Direct Asymmetric Aldol Reactions
    • List, B.; Lerner, R. A.; Barbas III, C. F. Proline-Catalyzed Direct Asymmetric Aldol Reactions. J. Am. Chem. Soc. 2000, 122, 2395-2396.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 2395-2396
    • List, B.1    Lerner, R.A.2    Barbas C.F. III3
  • 9
    • 0034596299 scopus 로고    scopus 로고
    • Catalytic Asymmetric Synthesis of Anti-1,2-Diols
    • Notz, W.; List, B. Catalytic Asymmetric Synthesis of anti-1,2-Diols. J. Am. Chem. Soc. 2000, 122, 7386-7387.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 7386-7387
    • Notz, W.1    List, B.2
  • 10
    • 0037134880 scopus 로고    scopus 로고
    • The First Direct and Enantioselective Cross-Aldol Reaction of Aldehydes
    • Northrup, A. B.; MacMillan, D. W. C. The First Direct and Enantioselective Cross-Aldol Reaction of Aldehydes. J. Am. Chem. Soc. 2002, 124, 6798-6799.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 6798-6799
    • Northrup, A.B.1    MacMillan, D.W.C.2
  • 11
    • 0000305933 scopus 로고
    • Unprecedent Asymmetric Aldol Reactions with Three Aldehyde Substrates Catalyzed by 2-Deoxyribose-5-phosphate Aldolase
    • Gijsen, H. J. M.; Wong, C.-H. Unprecedent Asymmetric Aldol Reactions with Three Aldehyde Substrates Catalyzed by 2-Deoxyribose-5-phosphate Aldolase. J. Am. Chem. Soc. 1994, 116, 8422-8423.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 8422-8423
    • Gijsen, H.J.M.1    Wong, C.-H.2
  • 13
    • 0036260164 scopus 로고    scopus 로고
    • Direct Organo-Catalytic Asymmetric α-Amination of Adehydes - A Simple Approach to Optically Active α-Amino Aldehydes, α-Amino Alcohols, and α-Amino Acid
    • Bøgevig, A.; Juhl, K.; Kumaragurubaran, N.; Zhuag, W.; Jørgensen, K. A. Direct Organo-Catalytic Asymmetric α-Amination of Adehydes-A Simple Approach to Optically Active α-Amino Aldehydes, α-Amino Alcohols, and α-Amino Acid. Angew. Chem. Int. Ed. 2002, 41, 1790-1793.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1790-1793
    • Bøgevig, A.1    Juhl, K.2    Kumaragurubaran, N.3    Zhuag, W.4    Jørgensen, K.A.5
  • 14
    • 0037157154 scopus 로고    scopus 로고
    • Direct Catalytic Asymmetric α-Amination of Aldehydes
    • List, B. Direct Catalytic Asymmetric α-Amination of Aldehydes. J. Am. Chem. Soc. 2002, 124, 5666-5667.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 5666-5667
    • List, B.1
  • 16
    • 0037416272 scopus 로고    scopus 로고
    • Proline-Catalyzed Asymmetric α-Amination of Aldehydes and Ketones - An Astonishingly Simple Access to Optically Active α-Hydrazino Carbonyl Compounds
    • Duthaler, R. O. Proline-Catalyzed Asymmetric α-Amination of Aldehydes and Ketones - An Astonishingly Simple Access to Optically Active α-Hydrazino Carbonyl Compounds. Angew. Chem. Int. Ed. 2003, 42, 975-978.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 975-978
    • Duthaler, R.O.1
  • 17
    • 0037028550 scopus 로고    scopus 로고
    • The Proline-Catalyzed Diret Asymmetric Three-Component Mannich Reaction: Scope, Optimization, and Application to the Highly Enantioselective Synthesis of 1,2-Amino Alcohols
    • (a) List, B.; Pojarliev, P.; Biller, W. T.; Martin, H. J. The Proline-Catalyzed Diret Asymmetric Three-Component Mannich Reaction: Scope, Optimization, and Application to the Highly Enantioselective Synthesis of 1,2-Amino Alcohols. J. Am. Chem. Soc. 2002, 124, 827-833.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 827-833
    • List, B.1    Pojarliev, P.2    Biller, W.T.3    Martin, H.J.4
  • 18
    • 0034721440 scopus 로고    scopus 로고
    • The Direct Catalytic Asymmetric Three-Component Mannich Reaction
    • (b) List, B. The Direct Catalytic Asymmetric Three-Component Mannich Reaction. J. Am. Chem. Soc. 2000, 122, 9336-9337.
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9336-9337
    • List, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.