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Volumn 16, Issue 38, 2010, Pages 11624-11631

A unified strategy targeting the thiodiketopiperazine mycotoxins exserohilone, gliotoxin, the epicoccins, the epicorazines, rostratin a and aranotin

Author keywords

Cycloaddition; Epithiodiketopiperazines; Metathesis; Natural products; Stereoselective synthesis

Indexed keywords

[2 + 2] CYCLOADDITION; ALLYL ACETATE; BUILDING BLOCKES; CYCLIC ENOL ETHER; CYCLOHEXENONES; DIASTEREOSELECTIVE; DIKETOPIPERAZINES; ENOL ETHERS; EPITHIODIKETOPIPERAZINES; METATHESIS; NATURAL PRODUCTS; PYROGLUTAMIC ACIDS; RING CLOSING METATHESIS; STEREOSELECTIVE SYNTHESIS; SYNTHETIC STRATEGIES;

EID: 77957549575     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201001169     Document Type: Article
Times cited : (38)

References (74)
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    • The configuration could be proven by NOESY experiments and was consistent with observations reported by Valle et al, see reference30 a
    • The configuration could be proven by NOESY experiments and was consistent with observations reported by Valle et al, see reference[30 a].
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    • 2, - 78°C we observed partial epimerisation to the cis-annelated system 10%
    • 2, - 78°C) we observed partial epimerisation to the cis-annelated system (10%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.