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Volumn 58, Issue 49, 2002, Pages 9839-9846

The diastereoselective asymmetric total synthesis of NG-391, a neuronal cell-protecting molecule

Author keywords

IBX oxidation; Knoevenagel reaction; Natural product; NG 391

Indexed keywords

ALCOHOL; ALDEHYDE DERIVATIVE; MALIC ACID; NEUROPROTECTIVE AGENT; NG 391; UNCLASSIFIED DRUG;

EID: 0037010766     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)01290-5     Document Type: Article
Times cited : (34)

References (20)
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    • (a) Hayashi Y., Narasaka K. Chem. Lett. 1998;313. The other total synthesis of epolactaene: (b) Marumoto S., Kogen H., Naruo S. J. Org. Chem. 63:1998;2068 (c) Marumoto S., Kogen H., Naruo S. Tetrahedron. 55:1999;7145 (d) Kuramochi K., Nagata S., Itaya H., Takano K., Kobayashi S. Tetrahedron Lett. 40:1999;7371.
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    • note
    • The reaction with diazomethane should be performed at low temperature because of the formation of the β-methoxy-α,β-unsaturated nitrile at 0°C.
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    • note
    • Aldehyde 16 was prepared from (S)-malic acid, see experimental section 1.2.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.