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Volumn 50, Issue 13, 2011, Pages 2962-2965

Total syntheses of guanacastepenes N and O

Author keywords

Cyclohexyne; Guanacastepene; Natural products; Total synthesis

Indexed keywords

CHEMICAL EQUATIONS; CORE STRUCTURE; CYCLOHEXYNE; GUANACASTEPENE; NATURAL PRODUCTS; PENTALENES; TOTAL SYNTHESIS;

EID: 79952634328     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201007644     Document Type: Article
Times cited : (54)

References (43)
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    • For a computational rationale of the observed selectivity, see
    • For a computational rationale of the observed selectivity, see P. H.-Y. Cheong, H. Yun, S. J. Danishefsky, K. N. Houk, Org. Lett. 2006, 8, 1513-1516.
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    • For a synthesis of enantiomerically enriched 7 in three steps, see Ref. [7]
    • For a synthesis of enantiomerically enriched 7 in three steps, see Ref. [7].
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    • For computational studies of the iron-mediated cyclobutene opening, see
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    • CCDC-785390 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC-785390 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc. cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.