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Volumn 12, Issue , 2010, Pages 107-136

Design of Catalysts for Asymmetric Organic Reactions Through Density Functional Calculations

Author keywords

Aldol reaction; Catalyst design; Density functional theory; Organocatalysis; Stereoselectivity; Sulfur ylide mediated reactions; Transition state

Indexed keywords


EID: 85018066637     PISSN: 25424491     EISSN: 25424483     Source Type: Book Series    
DOI: 10.1007/978-90-481-3034-4_4     Document Type: Chapter
Times cited : (4)

References (87)
  • 14
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    • List B (2002) Tetrahedron 58(28):5573–5590
    • (2002) Tetrahedron , vol.58 , Issue.28 , pp. 5573-5590
    • List, B.1
  • 42
    • 0034712223 scopus 로고    scopus 로고
    • (b) Taylor SK (2000) Tetrahedron 56(516):1149–1163
    • (2000) Tetrahedron , vol.56 , Issue.516 , pp. 1149-1163
    • Taylor, S.K.1
  • 44
    • 36849030755 scopus 로고    scopus 로고
    • and references therein
    • (b) Brackmann F, de Meijere A (2007) Chem Rev 107(11):4538–4583 and references therein
    • (2007) Chem Rev , vol.107 , Issue.11 , pp. 4538-4583
    • Brackmann, F.1    de Meijere, A.2
  • 62
  • 82
    • 85073218440 scopus 로고    scopus 로고
    • Different substituents on the ylidic center were chosen according to their electron withdrawing capacities. Based on literature reports and proton affinity evaluation, the various ylides have been classified into stabilized, semistabilized and non-stabilized categories (see ref. [60] for details)
    • Different substituents on the ylidic center were chosen according to their electron withdrawing capacities. Based on literature reports and proton affinity evaluation, the various ylides have been classified into stabilized, semistabilized and non-stabilized categories (see ref. [60] for details).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.