A short total synthesis of aureothin and N-acetylaureothamine.
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[1] C. Hertweck,et al. Formation of the aureothin tetrahydrofuran ring by a bifunctional cytochrome p450 monooxygenase. , 2004, Journal of the American Chemical Society.
[2] J. Baldwin,et al. An efficient synthesis of cyercene A , 2004 .
[3] C. Hertweck,et al. Biosynthetic origin of the rare nitroaryl moiety of the polyketide antibiotic aureothin: involvement of an unprecedented N-oxygenase. , 2004, Journal of the American Chemical Society.
[4] J. Baldwin,et al. Biomimetic studies on polyenes. , 2003, Organic & biomolecular chemistry.
[5] E. Negishi,et al. Clean inversion of configuration in the Pd-catalyzed cross-coupling of 2-bromo-1,3-dienes. , 2003, Journal of the American Chemical Society.
[6] R. Grubbs,et al. Synthesis of functionalized vinyl boronates via ruthenium-catalyzed olefin cross-metathesis and subsequent conversion to vinyl halides. , 2003, The Journal of organic chemistry.
[7] E. Negishi,et al. Highly selective synthesis of (E)-3-methyl-1-trialkylsilyl-3-en-1-ynes via trans-selective alkynylation catalyzed by Cl2Pd(DPEphos) and stereospecific methylation with methylzincs catalyzed by Pd(tBu3P)2. , 2003, Organic letters.
[8] A. Cowley,et al. Studies on the biomimetic synthesis of SNF4435 C and D. , 2002, Organic letters.
[9] A. V. Shastin,et al. A Novel Synthesis of ,-Dibromostyrenes , 2001 .
[10] M. Taniguchi,et al. Gamma-pyrone compounds with selective and potent anti-Helicobacter pylori activity. , 2000, The Journal of antibiotics.
[11] M. Gray,et al. Practical methylation of aryl halides by Suzuki-Miyaura coupling , 2000 .
[12] R. Kunz,et al. Use of thallium(I) ethoxide in Suzuki cross coupling reactions. , 2000, Organic letters.
[13] M. K. Basu,et al. Ultrasound-promoted highly efficient reduction of aromatic nitro compounds to the aromatic amines by samarium/ammonium chloride , 2000 .
[14] Robert H. Grubbs,et al. New Approaches to Olefin Cross-Metathesis , 2000 .
[15] K. Koyama,et al. A FORMAL TOTAL SYNTHESIS OF (+)-TETRONOLIDE, THE AGLYCON OF THE TETROCARCINS : ENANTIO- AND DIASTEREOSELECTIVE SYNTHESES OF THE OCTAHYDRONAPHTHALENE ( BOTTOM-HALF) AND SPIROTETRONATE (TOP-HALF) FRAGMENTS , 1997 .
[16] S. Nishiyama,et al. Absolute configuration of (+)-aureothin: A toxic metabolite possessing γ-pyrone unit , 1995 .
[17] S. Takano,et al. Enantioselective Synthesis of the α-Pyrone Subunit of Verrucosidin , 1993 .
[18] B. Trost,et al. Coordinative cocatalysis via indium(3+). A chemoselectivity switch for palladium-catalyzed cycloadditions , 1992 .
[19] Y. Shizuri,et al. Total synthesis of (+)-isoaureothin: determination of the absolute configurations of aureothin, isoaureothin and spectinabilin , 1992 .
[20] W. Roush,et al. Enantioselective synthesis of the bottom half of chlorothricolide. II: A comparative study of substituent effects on the stereoselectivity of the key intramolecular Diels-Alder reaction , 1988 .
[21] B. Trost,et al. Diastereoselective [3 + 2]-type heterocyclic synthesis via [2-(acetoxymethyl)-3-allyl]tri-n-butylstannane , 1985 .
[22] S. Ōmura,et al. Identification of mycolutein and pulvomycin as aureothin and labilomycin respectively. , 1976, The Journal of antibiotics.
[23] E. Suzuki,et al. A Facile Synthesis of 6-Conjugated 2-Pyrones , 1975 .
[24] K. Ando,et al. Pesticidal Activity of Aureothin , 1969 .
[25] H. Nakata,et al. The structure of aureothin, a nitro compound obtained from Streptomyces thioluteus , 1961 .
[26] R. Lemieux,et al. Notes - Osmium Tetroxide-Catalyzed Periodate Oxidation of Olefinic Bonds , 1956 .
[27] K. Maeda. Chemical studies on antibiotic substances. IV. A crystalline toxic substance of Streptomyces thioluteus producing aureothricin. , 1953, The Journal of antibiotics.