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Volumn 38, Issue 9, 1999, Pages 1263-1266

Total synthesis of (-)-mucocin

Author keywords

Annonins; Antitumor agents; Mucocin; Natural products; Total synthesis

Indexed keywords

ACETOGENIN; MUCOCIN; UNCLASSIFIED DRUG;

EID: 0033519292     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1521-3773(19990503)38:9<1263::AID-ANIE1263>3.0.CO;2-2     Document Type: Article
Times cited : (51)

References (38)
  • 6
    • 0032476126 scopus 로고    scopus 로고
    • Total syntheses of annonaceous acetogenins: a) J. A. Marshall, H. Jiang, J. Org. Chem. 1998, 63, 7066-7071;
    • (1998) J. Org. Chem. , vol.63 , pp. 7066-7071
    • Marshall, J.A.1    Jiang, H.2
  • 27
    • 33747539006 scopus 로고    scopus 로고
    • note
    • The bromodiol obtained in the dihydroxylation step cyclized easily to the hydroxytetrahydrofuran upon storage. Therefore it was instantly acetonide protected.
  • 33
    • 33747574937 scopus 로고    scopus 로고
    • note
    • The use of MeOH as a cosolvent gave the C24 methyl ether as the major by-product.
  • 35
    • 0001093255 scopus 로고
    • A. Wright, R. West, J. Am. Chem. Soc. 1974, 96, 3227-3232. A small deficit of tBuLi was beneficial to suppress the retro-Brook migration.
    • (1974) J. Am. Chem. Soc. , vol.96 , pp. 3227-3232
    • Wright, A.1    West, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.