메뉴 건너뛰기




Volumn 118, Issue 38, 1996, Pages 9017-9023

Ecteinascidins: Putative biosynthetic precursors and absolute stereochemistry

Author keywords

[No Author keywords available]

Indexed keywords

ECTEINASCIDIN; UNCLASSIFIED DRUG;

EID: 0029831192     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja950054m     Document Type: Article
Times cited : (89)

References (34)
  • 1
    • 10244266650 scopus 로고
    • Ph.D. Thesis, University of Illinois, Urbana
    • (a) Holt, T. G. Ph.D. Thesis, University of Illinois, Urbana, 1986; Diss. Abstr. Int. B 1987, 47, 3771-3772; Chem. Abstr. 1987, 106, 193149u.
    • (1986)
    • Holt, T.G.1
  • 2
    • 0346617503 scopus 로고
    • (a) Holt, T. G. Ph.D. Thesis, University of Illinois, Urbana, 1986; Diss. Abstr. Int. B 1987, 47, 3771-3772; Chem. Abstr. 1987, 106, 193149u.
    • (1987) Diss. Abstr. Int. B , vol.47 , pp. 3771-3772
  • 3
    • 10244220193 scopus 로고
    • (a) Holt, T. G. Ph.D. Thesis, University of Illinois, Urbana, 1986; Diss. Abstr. Int. B 1987, 47, 3771-3772; Chem. Abstr. 1987, 106, 193149u.
    • (1987) Chem. Abstr. , vol.106
  • 4
    • 10244231211 scopus 로고    scopus 로고
    • U.S. Patent 5,089,273, Feb. 18, 1992
    • (b) Rinehart, K. L.; Holt, T. G. U.S. Patent 5,089,273, Feb. 18, 1992; Chem. Abstr. 1992, 117, 63016q.
    • Rinehart, K.L.1    Holt, T.G.2
  • 5
    • 10244257899 scopus 로고
    • (b) Rinehart, K. L.; Holt, T. G. U.S. Patent 5,089,273, Feb. 18, 1992; Chem. Abstr. 1992, 117, 63016q.
    • (1992) Chem. Abstr. , vol.117
  • 8
    • 0346617501 scopus 로고
    • Kaul, P. N.; Sindermann, C. J., Eds., University of Oklahoma: Norman, OK
    • (e) Lichter, L.; Ghaffar, A.; Wellham, L. L.; Sigel, M. M. In Drugs & Food from the Sea; Kaul, P. N.; Sindermann, C. J., Eds., University of Oklahoma: Norman, OK, 1978; pp 137-144.
    • (1978) Drugs & Food from the Sea , pp. 137-144
    • Lichter, L.1    Ghaffar, A.2    Wellham, L.L.3    Sigel, M.M.4
  • 11
    • 10244238036 scopus 로고    scopus 로고
    • U.S. Patent 5,149,804; Sept. 22, 1992
    • (h) Rinehart, K.; Sakai, R.; U.S. Patent 5,149,804; Sept. 22, 1992; Chem. Abstr. 1992, 117, 205189z.
    • Rinehart, K.1    Sakai, R.2
  • 12
    • 10244245696 scopus 로고
    • (h) Rinehart, K.; Sakai, R.; U.S. Patent 5,149,804; Sept. 22, 1992; Chem. Abstr. 1992, 117, 205189z.
    • (1992) Chem. Abstr. , vol.117
  • 13
    • 10244255450 scopus 로고    scopus 로고
    • PharmaMar U.S., Cambridge, MA, personal communication to K. L. R.
    • G. Faircloth, PharmaMar U.S., Cambridge, MA, personal communication to K. L. R.
    • Faircloth, G.1
  • 17
    • 10244250647 scopus 로고
    • Ph.D. Thesis, University of Illinois, Urbana
    • (d) Sakai, R., Ph.D. Thesis, University of Illinois, Urbana, 1991.
    • (1991)
    • Sakai, R.1
  • 22
    • 10244227026 scopus 로고    scopus 로고
    • note
    • 3d
  • 23
    • 0029040573 scopus 로고
    • The present compounds (1-4) have been briefly described in a meeting report: Rinehart, K. L.; Tachibana, K. J. Nat. Prod. 1995, 58, 344-358.
    • (1995) J. Nat. Prod. , vol.58 , pp. 344-358
    • Rinehart, K.L.1    Tachibana, K.2
  • 24
    • 10244224388 scopus 로고    scopus 로고
    • note
    • - by negative FABMS failed (see ref le).
  • 26
    • 10244271014 scopus 로고    scopus 로고
    • note
    • 11
  • 28
    • 10244231210 scopus 로고    scopus 로고
    • note
    • IR absorption for the aα-keto group is expected to be small, since compound 1 exists mostly as the hemiketal or ketal in solution, as evidenced by FABMS. In the solid form, it may also exist, at least in part, as the hemiketal or ketal form.
  • 32
    • 0000669341 scopus 로고
    • Enzymatic reactions to form a methylenedioxy bridge have been demonstrated for plant-derived tetrahydroisoquinolines; cf. Bauer, W.; Zenk, M. H. Phytochemistry 1991, 30, 2953-2961.
    • (1991) Phytochemistry , vol.30 , pp. 2953-2961
    • Bauer, W.1    Zenk, M.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.