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Volumn 75, Issue 16, 2010, Pages 5764-5767

Total synthesis of batatoside L

Author keywords

[No Author keywords available]

Indexed keywords

EFFICIENT CONSTRUCTION; LARYNGEAL CARCINOMAS; MACROLACTONES; MACROLACTONIZATION; TOTAL SYNTHESIS;

EID: 77955707472     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101231r     Document Type: Article
Times cited : (24)

References (40)
  • 15
    • 33748222800 scopus 로고
    • For total synthesis of resin glycosides by a macrolactonization approach, see: Calonyctins
    • For total synthesis of resin glycosides by a macrolactonization approach, see: Calonyctins: Jiang, Z.-H.; Geyer, A.; Schmidt, R. R. Angew. Chem., Int. Ed. Engl. 1995, 34, 2520-2524
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2520-2524
    • Jiang, Z.-H.1    Geyer, A.2    Schmidt, R.R.3
  • 21
    • 0032489027 scopus 로고    scopus 로고
    • For the RCM method in total synthesis of resin glycosides, see: Tricolorins
    • For the RCM method in total synthesis of resin glycosides, see: Tricolorins: Fürstner, A.; Müller, T. J. Org. Chem. 1998, 63, 424-425
    • (1998) J. Org. Chem. , vol.63 , pp. 424-425
    • Fürstner, A.1    Müller, T.2
  • 29
    • 10244279191 scopus 로고    scopus 로고
    • 11(S)-Hydroxyhexadecanoic acid (jalapinolic acid) is available by hydrolysis of the crude convolvulaceous resins (ref 1a) and also by total synthesis, see: refs 10b-10g and
    • 11(S)-Hydroxyhexadecanoic acid (jalapinolic acid) is available by hydrolysis of the crude convolvulaceous resins (ref 1a) and also by total synthesis, see: refs 10b-10g and: Kitagawa, I.; Baek, N. I.; Kawashima, K.; Yokokawa, Y.; Yoshikawa, M.; Ohashi, K.; Shibuya, H. Chem. Pharm. Bull. 1996, 44, 1680-1692
    • (1996) Chem. Pharm. Bull. , vol.44 , pp. 1680-1692
    • Kitagawa, I.1    Baek, N.I.2    Kawashima, K.3    Yokokawa, Y.4    Yoshikawa, M.5    Ohashi, K.6    Shibuya, H.7
  • 40
    • 77955702677 scopus 로고    scopus 로고
    • An inverse Schmidt glycosylation has also played a key role in Fürstner's total synthesis of woodrosin I, see refs 11d and 11e
    • An inverse Schmidt glycosylation has also played a key role in Fürstner's total synthesis of woodrosin I, see refs 11d and 11e.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.