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Volumn 10, Issue 37, 2012, Pages 7503-7509

Concerted, highly asynchronous, enzyme-catalyzed [4 + 2] cycloaddition in the biosynthesis of spinosyn A; Computational evidence

Author keywords

[No Author keywords available]

Indexed keywords

[4 + 2] CYCLOADDITION; CYCLASES; DIELS-ALDERASE; DUAL ROLE; INTRINSIC REACTION COORDINATE CALCULATIONS; MODEL SYSTEM; MOLLER-PLESSET; NATURAL POPULATION ANALYSIS; POLARIZED TRANSITION; SECOND ORDERS; THEORETICAL STUDY; TRANSITION STATE; TRANSITION STRUCTURES;

EID: 84865700890     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob25827g     Document Type: Article
Times cited : (42)

References (35)
  • 7
    • 0037434992 scopus 로고    scopus 로고
    • T. Ose Nature 2003 422 185 189
    • (2003) Nature , vol.422 , pp. 185-189
    • Ose, T.1
  • 12
    • 79955621903 scopus 로고    scopus 로고
    • W. L. Kelly Nature 2011 473 35 36
    • (2011) Nature , vol.473 , pp. 35-36
    • Kelly, W.L.1
  • 35
    • 0011083499 scopus 로고
    • There appears to be some disagreement over the definition of a Diels-Alder reaction. A referee has commented, "a Diels-Alder reaction is defined as a reaction that yields a [4 + 2] cycloadduct regardless of mechanism." However, Kelly (ref. 12) states, "The hallmark of Diels-Alder [4 + 2] cycloadditions is that they are concerted - they proceed without forming any transient intermediates en route to the final product." We, as has Kim (ref. 2), have adopted the latter definition
    • A. E. Reed L. A. Curtiss F. Weinhold Chem. Rev. 1988 88 899 926
    • (1988) Chem. Rev. , vol.88 , pp. 899-926
    • Reed, A.E.1    Curtiss, L.A.2    Weinhold, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.