Total synthesis of (–)-ovalicin and analogues from L-quebrachitol
暂无分享,去创建一个
D. Barton | D. Billington | Derek H. R. Barton | Sophie Bath | David C. Billington | Stephan D. Gero | Béatrice Quiclet-Sire | Mohammad Samadi | B. Quiclet-Sire | M. Samadi | S. Gero | S. Bath
[1] Billington Dc. Angiogenesis and its inhibition: potential new therapies in oncology and non-neoplastic diseases. , 1991 .
[2] S. Gero. The preparation of 1-O-tosyl-(--)-inositol from quebrachitol. , 1966, Tetrahedron letters.
[3] Seiichiro Ogawa,et al. Utilisation of L-quebrachitol in natural product synthesis. Total synthesis and absolute configuration of (–)-oudemansin X , 1993 .
[4] H. P. Siǵǵ,et al. Die Struktur von Ovalicin , 1973 .
[5] D. Ingber,et al. Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth , 1990, Nature.
[6] E. Corey,et al. A New, Stereospecific Olefin Synthesis from 1,2-Diols , 1963 .
[7] S. Marui,et al. Chemical modification of fumagillin. II. 6-Amino-6-deoxyfumagillol and its derivatives. , 1992, Chemical & pharmaceutical bulletin.
[8] F. Itoh,et al. Chemical modification of fumagillin. I. 6-O-acyl, 6-O-sulfonyl, 6-O-alkyl, and 6-O-(N-substituted-carbamoyl)fumagillols. , 1992, Chemical & pharmaceutical bulletin.
[9] H. Okada,et al. Antitumor effects of angiogenesis inhibitor TNP-470 in rabbits bearing VX-2 carcinoma by arterial administration of microspheres and oil solution. , 1993, The Journal of pharmacology and experimental therapeutics.
[10] M. Okuhara,et al. A new angiogenesis inhibitor, FR-111142. , 1992, The Journal of antibiotics.
[11] R. Auerbach,et al. Angiogenesis inhibition: a review. , 1994, Pharmacology & therapeutics.
[12] C. Reese,et al. 2,4,6-Tri-isopropylbenzenesulphonyl hydrazide: A convenient source of di-imide , 1976 .
[13] A. Barrett,et al. Concise syntheses of 3-methylenetetrahydrofuran-2-one derivatives and related systems , 1982 .
[14] H. Weber,et al. [Isolation and structure elucidation of ovalicin]. , 1968, Helvetica chimica acta.
[15] E. Corey,et al. A total synthesis of ( )-fumagillin. , 1972, Journal of the American Chemical Society.
[16] James P. Dittami,et al. Total synthesis of (.+-.)-ovalicin , 1985 .
[17] A. Barrett,et al. Recent applications of the Shapiro reaction , 1983 .
[18] D. Cane,et al. Application of carbon-13 magnetic resonance to isoprenoid biosynthesis. II. Ovalicin and the use of doubly labeled mevalonate. , 1976, Journal of the American Chemical Society.
[19] T. Eble,et al. AN ANTIPHAGE AGENT ISOLATED FROM ASPERGILLUS SP , 1949, Journal of bacteriology.
[20] W. Zimmermann,et al. On the mode of action of the immunosuppressive sesquiterpene ovalicin. , 1981, European journal of biochemistry.
[21] D. Ingber,et al. Potent anti-angiogenic action of AGM-1470: comparison to the fumagillin parent. , 1991, Biochemical and biophysical research communications.
[22] J. Lawlis,et al. Fumagillin (H-3), a new antibiotic with amebicidal properties. , 1951, Science.