메뉴 건너뛰기




Volumn 70, Issue 12, 2014, Pages 2096-2101

Enantioselective synthesis of macrolactone core of the natural product Sch725674

Author keywords

Macrolide; Natural products; Sch725674; Total synthesis

Indexed keywords

FURFURAL; LACTONE DERIVATIVE; MACROLACTONE; NATURAL PRODUCT; SCH 725674; UNCLASSIFIED DRUG;

EID: 84896737140     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2014.02.008     Document Type: Article
Times cited : (19)

References (21)
  • 17
    • 33947094130 scopus 로고
    • 1H NMR spectrum when 14 was converted to 15 which was also a non-separable mixture. This diastereomeric mixture was used as such in the next step. Separation of the major diastereomer 17 was accomplished in the TES deprotection of 16 in 54% yield
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 2226
    • Luche, J.L.1
  • 20
    • 84896699638 scopus 로고    scopus 로고
    • PhD thesis, University of Pittsburg
    • Moretti, J. D. PhD thesis, University of Pittsburg, 2010.
    • (2010)
    • Moretti, J.D.1
  • 21
    • 84896720623 scopus 로고    scopus 로고
    • PhD thesis, University of Pittsburg
    • Wang, X. PhD thesis, University of Pittsburg, 2009.
    • (2009)
    • Wang, X.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.