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Volumn 22, Issue 2, 2011, Pages 246-251

Formal total synthesis of aspergillide A

Author keywords

[No Author keywords available]

Indexed keywords

( 9 TERT BUTYLDIMETHYLSILYLOXY) 1 ( 1,3 DITHIAN 2 YL)DEC 4 EN 3 OL; ( 9 TERT BUTYLDIMETHYLSILYLOXY) 1 ( 1,3 DITHIAN 2 YL)DEC 4 EN 3 ONE; 2 ( 6 ( 6 HYDROXYHEPT 1 ENYL) 3 METHOXY METHYLOXYTETRAHYDRO 2H PYRAN 2 YL)ACETIC ACID; 5 ( 1,3 DITHIAN 2 YL)PENT 1 EN 3 ONE; ACETIC ACID DERIVATIVE; ACRYLIC ACID DERIVATIVE; ALKENE; ALLYL ALCOHOL; ASPERGILLIDE A; BETA ALKOXYACRYLIC ACID; CARBON; DECANOIC ACID DERIVATIVE; ETHYL 2 ( 6 ( 6 (TERT BUTYLDIMETHYLSILYLOXY)HEPT 1 ENYL) 3 METHOXYMETHYLOXYTETRAHYDRO 2H PYRAN 2 YL)ACETIC ACID; ETHYL 3 ( 9 (TERT BUTYLDIMETHYLSILYLOXY) 1 OXOUNDEC 5 EN 4 YLOXY)PROPN 2 ENOIC ACID; HEPTANE DERIVATIVE; MACROLIDE; SAMARIUM DIIODIDE; TETRAHYDROPYRAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79952488127     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2011.01.016     Document Type: Article
Times cited : (24)

References (30)
  • 13
    • 79952486826 scopus 로고    scopus 로고
    • The carbon-numbering system is according to the one shown in Ref. 12
    • The carbon-numbering system is according to the one shown in Ref. 12.
  • 29
    • 79952489644 scopus 로고    scopus 로고
    • note
    • 13 of 18 by NMR analyses whereas the higher polar one was revealed to be a complex mixture including 3 and 18 (∼29%).
  • 30
    • 79952489930 scopus 로고    scopus 로고
    • At -78 °C, the reaction was very sluggish and a considerable amount of starting material remained
    • At -78 °C, the reaction was very sluggish and a considerable amount of starting material remained.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.