메뉴 건너뛰기




Volumn 38, Issue 47, 1997, Pages 8241-8244

Studies in marine macrolide synthesis: Synthesis of the C1-C15 subunit of spongistatin 1 (altohyrtin A) and 15,16-anti aldol coupling reactions

Author keywords

[No Author keywords available]

Indexed keywords

ANTIMITOTIC AGENT; MACROLIDE; SPONGISTATIN 1; UNCLASSIFIED DRUG;

EID: 0030703550     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)10126-5     Document Type: Article
Times cited : (66)

References (29)
  • 8
    • 0029857429 scopus 로고    scopus 로고
    • Some of the altohyrtin macrolides reported in the following papers are assumed to be structurally identical to the spongistatins (i.e. altohyrtin A corresponds to spongistatin 1): (a) Kobayashi, M.; Aoki, S.; Gato, K.; Kitagawa, I. Chem. Pharm. Bull. 1996, 44, 2142.
    • (1996) Chem. Pharm. Bull. , vol.44 , pp. 2142
    • Kobayashi, M.1    Aoki, S.2    Gato, K.3    Kitagawa, I.4
  • 12
    • 0027244662 scopus 로고
    • Cinachyrolide A, isolated from a sponge of the genus Cinachyra, is assumed to be structurally identical to spongistatin 4: Fusetani, N.; Shinoda, K.; Matsunaga, S. J. Am. Chem. Soc. 1993, 115, 3977.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 3977
    • Fusetani, N.1    Shinoda, K.2    Matsunaga, S.3
  • 20
    • 0001790298 scopus 로고    scopus 로고
    • For a review of asymmetric aldol reactions using boron enolates, see: Cowden, C. J.; Paterson, I. Org. React. 1997, 51, 1.
    • (1997) Org. React. , vol.51 , pp. 1
    • Cowden, C.J.1    Paterson, I.2
  • 21
    • 85036682339 scopus 로고    scopus 로고
    • note
    • 15) (cf. 5.12, dd, J = 1.7, 11), 6.90 (2H, d, J = 8.6 Hz, Ar, 7.26 (2H, d, J = 8.6 Hz, Ar).
  • 23
    • 85036684389 scopus 로고    scopus 로고
    • note
    • iPrMgCl, THF, -20 °C, 1 h; and (iii) MeMgBr, THF, 0 °C → 20 °C, 2 h.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.