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Drug Discovery Today
Volumn 18, Issue 17-18, 2013, Pages 795-802
A remote-controlled adaptive medchem lab: An innovative approach to enable drug discovery in the 21st Century
Author keywords

[No Author keywords available]
Indexed keywords

CASE STUDY; CHEMISTRY; COMPUTER; COMPUTER PROGRAM; DRUG SYNTHESIS; LABORATORY; LABORATORY AUTOMATION; MICROWAVE IRRADIATION; PURIFICATION; REVIEW;
EID: 84883258908     PISSN: 13596446     EISSN: 18785832     Source Type: Journal    
DOI: 10.1016/j.drudis.2013.03.001     Document Type: Short Survey
Times cited : (109)
References (10)
  • 1
    • 0036427644 scopus 로고    scopus 로고
    • Accelerating drug discovery by integrative implementation of laboratory automation in the work flow
    • M. Nettekoven, and A.W. Thomas Accelerating drug discovery by integrative implementation of laboratory automation in the work flow Curr. Med. Chem. 9 2002 2179 2190
    • (2002) Curr. Med. Chem. , vol.9 , pp. 2179-2190
    • Nettekoven, M.1    Thomas, A.W.2
  • 2
    • 0034326432 scopus 로고    scopus 로고
    • Successful implementation of automation in medicinal chemistry
    • W.J. Coates Successful implementation of automation in medicinal chemistry Drug Discov. Today 5 2000 521 527
    • (2000) Drug Discov. Today , vol.5 , pp. 521-527
    • Coates, W.J.1
  • 3
    • 72449133296 scopus 로고    scopus 로고
    • An efficient laboratory automation concept for process chemistry
    • C. Bernlind, and C. Urbaniczky An efficient laboratory automation concept for process chemistry Org. Process Res. Dev. 13 2009 1059 1067
    • (2009) Org. Process Res. Dev. , vol.13 , pp. 1059-1067
    • Bernlind, C.1    Urbaniczky, C.2
  • 4
    • 17144431405 scopus 로고    scopus 로고
    • SynCar: An approach to automated synthesis
    • A. Weber SynCar: an approach to automated synthesis J. Comb. Chem. 7 2005 178 184
    • (2005) J. Comb. Chem. , vol.7 , pp. 178-184
    • Weber, A.1
  • 6
    • 27644469374 scopus 로고    scopus 로고
    • New multi-component reaction accessing 3-aminoimidazo[1,2-a]pyridines
    • J. Schwerkoske New multi-component reaction accessing 3-aminoimidazo[1,2-a]pyridines Tetrahedron Lett. 46 2005 8355 8357
    • (2005) Tetrahedron Lett. , vol.46 , pp. 8355-8357
    • Schwerkoske, J.1
  • 7
    • 33645231449 scopus 로고    scopus 로고
    • Sequential Ugi/Strecker reactions via microwave assisted organic synthesis: Novel 3-center-4-component and 3-center-5-component multi-component reactions
    • T. Masquelin Sequential Ugi/Strecker reactions via microwave assisted organic synthesis: novel 3-center-4-component and 3-center-5-component multi-component reactions Tetrahedron Lett. 47 2006 2989 2991
    • (2006) Tetrahedron Lett. , vol.47 , pp. 2989-2991
    • Masquelin, T.1
  • 8
    • 84883225285 scopus 로고    scopus 로고
    • Facile access to a range of heterocyclic chemo-types via a novel combination of flow hydrogenation and microwave incubation processes
    • Chicago, IL, United States, March 25-29, 2007 American Chemical Society
    • A.G. Godfrey Facile access to a range of heterocyclic chemo-types via a novel combination of flow hydrogenation and microwave incubation processes 233rd ACS National Meeting Chicago, IL, United States, March 25-29, 2007 2007 American Chemical Society ORGN 207
    • (2007) 233rd ACS National Meeting , pp. 207
    • Godfrey, A.G.1
  • 9
    • 45149102410 scopus 로고    scopus 로고
    • Ugi-Smiles access to quinoxaline derivatives
    • J. Oble Ugi-Smiles access to quinoxaline derivatives Heterocycles 73 2007 503 517
    • (2007) Heterocycles , vol.73 , pp. 503-517
    • Oble, J.1
  • 10
    • 29144448797 scopus 로고    scopus 로고
    • Phenol Ugi-Smiles systems: Strategies for the multicomponent N-arylation of primary amines with isocyanides, aldehydes, and phenols
    • K.L. El Phenol Ugi-Smiles systems: strategies for the multicomponent N-arylation of primary amines with isocyanides, aldehydes, and phenols Angew. Chem. Int. Ed. 44 2005 7961 7964
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 7961-7964
    • El, K.L.1

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.