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Volumn , Issue 17, 2009, Pages 2847-2854

Structure investigations of (ent)-cladospolide d by de novo synthesis and kinetic and thermodynamic isomerization

Author keywords

Asymmetric synthesis; Cladospolides B D; E Z alkene isomerization; Natural product synthesis

Indexed keywords

ASYMMETRIC SYNTHESIS; CLADOSPOLIDES B-D; DE NOVO SYNTHESIS; DIHYDROXYLATION; E/Z-ALKENE ISOMERIZATION; NATURAL PRODUCT SYNTHESIS; NATURAL PRODUCTS; REGIO-SELECTIVE;

EID: 70449411221     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1217606     Document Type: Article
Times cited : (17)

References (44)
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    • For the synthesis of cladospolide B, see:
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    • For the synthesis of cladospolide D, see ref. 3c and:
    • For the synthesis of cladospolide D, see ref. 3c and: Lu, K.-J.; Chen, C.-H.; Hou, D.-R. Tetrahedron 2009, 65, 225.
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    • The regioselectivity of the asymmetric dihydroxylation of dienoates has been studied by Sharpless and our group, see: Berker, H.; Soler, M. A.; Sharpless, K. B. Tetrahedron 1995, 51, 1345.
    • (1995) Tetrahedron , vol.51 , pp. 1345
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    • For synthetic application of this, see
    • For synthetic application of this, see: Hunter, T. J.; O'Doherty, G. A. Org. Lett. 2002, 4, 4447.
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    • Li, M.1    O'Doherty, G.A.2
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    • For its use in synthesis, see:
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    • Guo, H.1    O'Doherty, G.A.2
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    • note
    • The double bond stereochemistry for four potential diastereomers of cladospolide D 18-21 were conclusively assigned by examination of the C2/C3 H-H coupling constants (for the E-isomers, 18, J = 16.2 Hz; 19, J = 16.2 Hz; and for the Z-isomers 20, J = 13.2 Hz and 21, J = 13.2 Hz).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.