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Volumn 6, Issue 2, 2011, Pages 560-572

Total synthesis of dictyodendrins A-E

Author keywords

arynes; cross coupling; cyclization; natural products; total synthesis

Indexed keywords

ARYNES; BENZYNE; CROSS-COUPLINGS; NATURAL PRODUCTS; ONE POT; SYNTHESIS FEATURES; TOTAL SYNTHESIS;

EID: 79251493789     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.201000544     Document Type: Article
Times cited : (60)

References (79)
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    • A benzyne species would be generated between -20 and 0°C in this case, as most of the starting material was recovered when the reaction was run below -20°C.
    • A benzyne species would be generated between -20 and 0°C in this case, as most of the starting material was recovered when the reaction was run below -20°C.
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    • 2 • 2 LiBr has been used as a selective deprotonating reagent; however, it has not been used for benzyne generation
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    • 4].
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    • Attempted cross-coupling reaction after benzyne formation/cyclization with the cuprate (Table 1, entry 2) base resulted in the generation of protio-indoline 32.
    • Attempted cross-coupling reaction after benzyne formation/cyclization with the cuprate (Table 1, entry 2) base resulted in the generation of protio-indoline 32.
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    • Preparation of 44 is described in the Supporting Information.
    • Preparation of 44 is described in the Supporting Information.
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    • The synthesis of azidephenyl iodide 50 was carried out from commercially available ortho-fluoronitrobenzene in six steps. For details, see the Supporting Information.
    • The synthesis of azidephenyl iodide 50 was carried out from commercially available ortho-fluoronitrobenzene in six steps. For details, see the Supporting Information.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.