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Volumn 132, Issue 40, 2010, Pages 14212-14215

Total synthesis of plukenetione A

Author keywords

[No Author keywords available]

Indexed keywords

ADAMANTANES; ALLYLIC ALCOHOL; CYCLIZATIONS; FACILE ACCESS; NATURAL PRODUCTS; TOTAL SYNTHESIS;

EID: 77957690642     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja105784s     Document Type: Article
Times cited : (69)

References (41)
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    • Presented in part at the 238rd American Chemical Society National Meeting, Aug 18-23, 2009, Washington DC,; abstract ORGN 595.
  • 11
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    • See Supporting Information for complete experimental details
    • See Supporting Information for complete experimental details.
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    • For a review of NCS-mediated reactions, see
    • For a review of NCS-mediated reactions, see: Golebiewski, W. M. and Gucma, M. Synthesis 2007, 23, 3599
    • (2007) Synthesis , vol.23 , pp. 3599
    • Golebiewski, W.M.1    Gucma, M.2
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    • 53749105476 scopus 로고    scopus 로고
    • For rearomatization of dearomatized acylphloroglucinols, see
    • For rearomatization of dearomatized acylphloroglucinols, see: Raikar, S., Nuhant, P., Delpech, B., and Marazano, C. Eur. J. Org. Chem. 2008, 8, 1358
    • (2008) Eur. J. Org. Chem. , vol.8 , pp. 1358
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    • 77957705819 scopus 로고    scopus 로고
    • Anhydrous HCl was also examined with substrates 16 and 19 at room temperature, leading to recovery of starting materials after 2 days
    • Anhydrous HCl was also examined with substrates 16 and 19 at room temperature, leading to recovery of starting materials after 2 days.
  • 36
    • 77957707635 scopus 로고    scopus 로고
    • According to the insightful recommendation of a reviewer, demethylation of intermediates 29 and 32 may also occur by hydrolysis of oxonium intermediates produced after cyclization
    • According to the insightful recommendation of a reviewer, demethylation of intermediates 29 and 32 may also occur by hydrolysis of oxonium intermediates produced after cyclization.
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    • Molander, G.1    McKie, J.2    Chung, K.3    Chu, C.4    Chang, M.5
  • 39
    • 34447324093 scopus 로고    scopus 로고
    • N2 reactivity in metal triflate-catalyzed alkylations, see
    • N2 reactivity in metal triflate-catalyzed alkylations, see: Noji, M., Konno, Y., and Ishii, Y. J. Org. Chem. 2007, 72, 5161
    • (2007) J. Org. Chem. , vol.72 , pp. 5161
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    • (1998) J. Org. Chem. , vol.63 , pp. 4654
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.