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Volumn 14, Issue 14, 2012, Pages 3696-3699

Toward the total synthesis of palhinine A: Expedient assembly of multifunctionalized isotwistane ring system with contiguous quaternary stereocenters

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; PALHININE A; POLYCYCLIC HYDROCARBON;

EID: 84864146515     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol301534r     Document Type: Article
Times cited : (30)

References (63)
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    • For selected examples on the construction of the isotwistane core via Pinacol coupling from the bicyclo[2.2.2]octane system, see: Yoshimitsu, T.; Sasaki, S.; Arano, Y.; Nagaoka, H. J. Org. Chem. 2004, 69, 9262
    • (2004) J. Org. Chem. , vol.69 , pp. 9262
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    • references therein
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    • Roush, W.R.1
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    • For a four-step synthetic protocol to access the enone 6, see the Supporting Information. Literaturally, the enone 6 was already known: Taber, D. F.; Sheth, R. B. J. Org. Chem. 2008, 73, 8030
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  • 53
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    • The chiral 7 could be also accessed by a formal asymmetric conjugate allylation of enones recently reported by Taber et al. This synthetically available chiral synthon will alternatively lead the way for the future study of asymmetric synthesis of palhinine A. Taber, D. F.; Gerstenhaber, D. A.; Berry, J. F. J. Org. Chem. 2011, 76, 7614
    • (2011) J. Org. Chem. , vol.76 , pp. 7614
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.