Absolute stereochemistry of the strevertenes.
暂无分享,去创建一个
[1] R. W. Hoffmann,et al. Conformation preferences in 2,4,6-trisubstituted heptanes☆ , 1999 .
[2] G. Carter,et al. Strevertenes, antifungal pentaene macrolides produced by Streptoverticillcum LL-30F848 , 1999 .
[3] T. I. Richardson,et al. Configurational Assignment of Polyene Macrolide Antibiotics Using the [13C]Acetonide Analysis , 1998 .
[4] T. I. Richardson,et al. TOTAL SYNTHESIS OF FILIPIN III , 1997 .
[5] S. Rychnovsky,et al. Two-Dimensional NMR Analysis of Acetonide Derivatives in the Stereochemical Assignment of Polyol Chains: The Absolute Configurations of Dermostatins A and B. , 1997, The Journal of organic chemistry.
[6] G. Schlewer,et al. Synthesis of α-Trinositol Analogues Derived from D-(-)-Quinic Acid as Affinity Probe Precursors , 1997 .
[7] T. I. Richardson,et al. Filipin III: Configuration Assignment and Confirmation by Synthetic Correlation. , 1996, The Journal of organic chemistry.
[8] H. Furukawa,et al. A Simple Strategy for Determining the Absolute Configurations of Acyclic 1,2,4,6,8-Pentols. , 1996 .
[9] K. Nakanishi,et al. The Exciton Chirality Method , 1995 .
[10] S. Rychnovsky. Oxo Polyene Macrolide Antibiotics , 1995 .
[11] T. I. Richardson,et al. Relative and Absolute Configuration of Filipin III , 1995 .
[12] H. Furukawa,et al. A difference CD method for determining absolute stereochemistry of acyclic 1,2,4-triols , 1995 .
[13] K. Nakanishi,et al. ALLYLIC AND HOMOALLYLIC EXCITON COUPLED CD : A SENSITIVE METHOD FOR DETERMINING THE ABSOLUTE STEREOCHEMISTRY OF NATURAL PRODUCTS , 1995 .
[14] J. Lancelin,et al. Stereostructure of glycosylated polyene macrolides : the example of pimaricin , 1995 .
[15] K. Nakanishi,et al. Combined synthetic/CD strategy for the preparation and configurational assignments of model acyclic 1,3-polyols with a 1,2-diol terminal. , 1995, Chirality.
[16] K. Nakanishi,et al. Absolute stereochemistry of natural 3,4-dihydroxy-beta-ionone glycosides by the CD exciton chirality method. , 1994, Journal of natural products.
[17] S. Rychnovsky,et al. Stereochemical Assignment of Roflamycoin by 13C Acetonide Analysis , 1994 .
[18] K. Nakanishi,et al. Intracellular signaling activity of synthetic (14R)-, (14S)-, and (14RS)-14-hydroxy-4,14-retro-retinol. , 1994, Biochemistry.
[19] K. Nakanishi,et al. CD Exciton Chirality Method. New Red‐Shifted Chromophores for Hydroxyl Groups. , 1993 .
[20] E. Borowski,et al. Stereostructure and NMR characterization of the antibiotic candidin. , 1993, The Journal of antibiotics.
[21] K. Nakanishi,et al. A chiroptical/chemical strategy for configurational assignments of acyclic 1,3-skipped polyols: model 1,2,4,6-tetrols , 1993 .
[22] K. Easwaran,et al. Conformation of polyene antibiotic, filipin III: CD and 1H NMR studies. , 1993, Journal of biomolecular structure & dynamics.
[23] K. Nakanishi,et al. Circular dichroism exciton chirality method. New red-shifted chromophores for hydroxyl groups , 1993 .
[24] K. Nakanishi,et al. Assignment of relative and absolute configuration of acyclic polyols and aminopolyols by circular dichroism - trends follow fischer's sugar family tree , 1993 .
[25] Makoto Suzuki,et al. Determination of absolute stereochemistry of acyclic 1,3-polyols by a difference CD method , 1992 .
[26] E. Borowski,et al. 1H NMR model studies of amphotericin B: Comparison of x‐ray and NMR stereochemical data , 1992 .
[27] Hiroshi Ono,et al. A CD method for determination of the absolute stereochemistry of acyclic glycols. 1. Application of the CD exciton chirality method to acyclic 1,3-dibenzoate systems , 1991 .
[28] J. Lancelin,et al. Stereostructure of pimaricin , 1990 .
[29] P. Joseph-Nathan,et al. Preparation of new quinic acid boron esters in aprotic media , 1990 .
[30] E. Borowski,et al. The structure of vacidin A, an aromatic heptaene macrolide antibiotic. II. Stereochemistry of the antibiotic. , 1989, The Journal of antibiotics.
[31] E. Borowski,et al. The structure of vacidin A, an aromatic heptaene macrolide antibiotic. I. Complete assignment of the 1H NMR spectrum and geometry of the polyene chromophore. , 1989, The Journal of antibiotics.
[32] M. Hatada,et al. Microbial products. 9. Roxaticin, a new oxo pentaene antibiotic , 1989 .
[33] T. Ōishi. Studies directed towards the stereoselective synthesis of polyene macrolide antibiotics , 1989 .
[34] J. Prandi,et al. Stereostructure of nystatin A1: A synthetic assignment of the C1–C10 fragment , 1989 .
[35] J. Lancelin,et al. Complete stereostructure of nystatin A1: A proton NMR study , 1989 .
[36] K. Nakanishi,et al. Stereochemical Studies of Polyols from the Polyene Macrolide Lienomycin. , 1988 .
[37] S. Schreiber,et al. Application of the two-directional chain synthesis strategy to the first stereochemical assignment of structure to members of the skipped-polyol polyene macrolide class: mycoticin A and B , 1987 .
[38] Y. Hamada,et al. New Methods and Reagents in Organic Synthesis. Part 71. A Facile Synthesis of Ulicyclamide (I). , 1987 .
[39] S. Schreiber,et al. Stereochemical studies of the skipped-polyol polyene macrolide class: NMR studies of a tetraformylal derivative of mycoticin A and B. , 1987 .
[40] S. Schreiber,et al. Stereochemical studies of the skipped-polyol polyene macrolide class: Degradation and partial structure determination of mycoticin A and B. , 1987 .
[41] Y. Hamada,et al. New methods and reagents in organic synthesis. 58. , 1985 .
[42] K. Nakanishi,et al. Circular dichroic spectroscopy : exciton coupling in organic stereochemistry , 1983 .
[43] K. Nakanishi,et al. GENERAL METHOD FOR DETERMINING ABSOLUTE CONFIGURATION OF ACYCLIC ALLYLIC ALCOHOLS , 1982 .
[44] T. Shioiri,et al. New Methods and Reagents in Organic Synthesis. 14. A Simple Efficient Preparation of Methyl Esters with Trimethylsilyldiazomethane (TMSCHN2) and Its Application to Gas Chromatographic Analysis of Fatty Acids , 1981 .
[45] J. Fréchet,et al. Use of polymers as protecting groups in organic synthesis. Application of polystyrylboronic acid to the one-pot synthesis of acylated carbohydrate derivatives , 1979 .
[46] C. Schaffner,et al. Polyene macrolide antibiotic amphotericin B. Crystal structure of the N-iodoacetyl derivative. , 1971, Journal of the American Chemical Society.
[47] C. Schaffner,et al. Structure and absolute configuration of the polyene macrolide antibiotic amphotericin B , 1970 .