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Volumn 51, Issue 1, 2010, Pages 96-98

An expeditious total synthesis of (±)-jamtine using condensation between imine and acid anhydride

Author keywords

Acid anhydride condensation; Imine condensation; Isoquinoline alkaloid; Jamtine; Microwave assisted synthesis; Natural product synthesis; Pyrroloisoquinoline

Indexed keywords

6,7 DIMETHOXY 3,4 DIHYDROISOQUINOLINE; ACID ANHYDRIDE; ALKALOID DERIVATIVE; IMINE; JAMTINE; TETRAHYDROPHTHALIC ACID ANHYDRIDE; UNCLASSIFIED DRUG;

EID: 70649086234     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.10.091     Document Type: Article
Times cited : (23)

References (26)
  • 11
    • 70649110833 scopus 로고    scopus 로고
    • Preliminary Communication at the XIIth ICSN Symposium: 'From Organic Chemistry to Chemical Biology', July 11-12th, 2009. Gif-sur-Yvette, France.
    • Preliminary Communication at the XIIth ICSN Symposium: 'From Organic Chemistry to Chemical Biology', July 11-12th, 2009. Gif-sur-Yvette, France.
  • 14
    • 70649109469 scopus 로고    scopus 로고
    • note
    • ar); 169.7 (CO); 173.4 (CO).
  • 21
    • 70649098678 scopus 로고    scopus 로고
    • note
    • 4 and concentrated in vacuo.
  • 22
    • 70649110831 scopus 로고    scopus 로고
    • note
    • ar); 171.3 (CO); 173.4 (CO).
  • 24
    • 70649084505 scopus 로고    scopus 로고
    • note
    • The syn isomer is characterized by a strong upfield shift of the methyl group of the ester; see Ref. 2a.
  • 25
    • 70649098677 scopus 로고    scopus 로고
    • note
    • 12b) after examination of the NMR spectra of the mixture 8a-c.
  • 26
    • 70649083601 scopus 로고    scopus 로고
    • note
    • 5 who mentioned some doubt on the structure of the natural product.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.