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Volumn 129, Issue 41, 2007, Pages 12453-12460

16-Aza-ent-beyerane and 16-aza-ent-trachylobane: Potent mechanism-based inhibitors of recombinant ent-kaurene synthase from Arabidopsis thaliana

Author keywords

[No Author keywords available]

Indexed keywords

ARABIDOPSIS THALIANA; CYCLIC STRUCTURES; INHIBITION CONSTANTS; MECHANISTIC HYPOTHESES;

EID: 35348947451     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja072447e     Document Type: Article
Times cited : (65)

References (93)
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    • All beyerane, kaurane, and trachylobane derivatives prepared or discussed in this paper belong to the enantiomeric (ent) family of biogenetically related diterpenes. The ent prefix descriptor is attached to the chemical names (eg, ent-beyerane, ent-kaurane, ent-trachylbane) frequently in the text to remind the reader of the absolute configuration. Complete semisystematic names are given as headings in the Experimental Section and Supporting Information. For IUPAC nomenclature guidelines, see: Riguady, J, Klesney, S. P. Nomenclature of Organic Chemistry, Sections A, B, C, D, E, F, and H; Pergamon: Oxford, 1979, and ref 2b
    • All beyerane, kaurane, and trachylobane derivatives prepared or discussed in this paper belong to the enantiomeric (ent) family of biogenetically related diterpenes. The ent prefix descriptor is attached to the chemical names (eg, ent-beyerane, ent-kaurane, ent-trachylbane) frequently in the text to remind the reader of the absolute configuration. Complete semisystematic names are given as headings in the Experimental Section and Supporting Information. For IUPAC nomenclature guidelines, see: Riguady, J.; Klesney, S. P. Nomenclature of Organic Chemistry, Sections A, B, C, D, E, F, and H; Pergamon: Oxford, 1979, and ref 2b.
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    • Selected X-ray crystal structures of aziridines: (a) Chinnakali, K.; Fun, H.-K.; Sriraghavan, K.; Ramakrishnan, V. T.; Razak, I. A. Acta Crystallogr. 1998, C54, 1299-1301.
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    • The IUPAC nomenclature was followed according to which the α or β configuration of substituents in ent-diterpenes is that designated in the systematic name for the normal antipode. See Rigaudy, J, Klesney, S. P. Nomenclature of Organic Chemistry, Sections A, B, C, D, E, F, and H; Pergamon Press: Oxford, 1979; p 511
    • The IUPAC nomenclature was followed according to which the α or β configuration of substituents in ent-diterpenes is that designated in the systematic name for the "normal" antipode. See Rigaudy, J.; Klesney, S. P. Nomenclature of Organic Chemistry, Sections A, B, C, D, E, F, and H; Pergamon Press: Oxford, 1979; p 511.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.