Biosynthetic Pathway and Origin of the Chlorinated Methyl Group in Barbamide and Dechlorobarbamide, Metabolites from the Marine Cyanobacterium Lyngbya majuscula

[1]  W. Gerwick,et al.  Biosynthesis of the marine cyanobacterial metabolite barbamide. 2: Elucidation of the origin of the thiazole ring by application of a new GHNMBC experiment , 1999 .

[2]  N. Kelleher,et al.  Assembly line enzymology by multimodular nonribosomal peptide synthetases: the thioesterase domain of E. coli EntF catalyzes both elongation and cyclolactonization. , 1999, Chemistry & biology.

[3]  G. Harrigan,et al.  Symplostatin 1: A dolastatin 10 analogue from the marine cyanobacterium Symploca hydnoides. , 1998, Journal of natural products.

[4]  W. Gerwick,et al.  Biosynthesis of the marine cyanobacterial metabolite barbamide. 1. Origin of the trichloromethyl group , 1998 .

[5]  M. Garson,et al.  New chlorinated metabolites from the tropical marine sponge Dysidea herbacea , 1997 .

[6]  A. J. Shaka,et al.  One-Dimensional NOE Experiments Using Pulsed Field Gradients , 1997 .

[7]  H. Seto,et al.  Simultaneous operation of the mevalonate and non-mevalonate pathways in the biosynthesis of isopentenly diphosphate in Streptomyces aeriouvifer , 1996 .

[8]  W. Gerwick,et al.  Barbamide, a chlorinated metabolite with molluscicidal activity from the Caribbean cyanobacterium Lyngbya majuscula. , 1996, Journal of natural products.

[9]  R. Reid,et al.  Methods for the Synthesis of L-Leucine Selectively Labelled with Carbon-13 or Deuterium in either Diastereotopic Methyl Group , 1995 .

[10]  G. Martin,et al.  Long‐range 1H‐15N correlation at natural abundance using gradient‐enhanced inverse‐detection , 1995 .

[11]  S. Carmeli,et al.  Biosynthesis of tolytoxin. Origin of the carbons and heteroatoms , 1993 .

[12]  C. Ireland,et al.  Patellamide E: a new cyclic peptide from the ascidian Lissoclinum patella. , 1992, Journal of natural products.

[13]  Kenneth B. Tomer,et al.  The isolation and structure of a remarkable marine animal antineoplastic constituent: dolastatin 10 , 1987 .

[14]  A. Bax,et al.  1H and13C Assignments from Sensitivity-Enhanced Detection of Heteronuclear Multiple-Bond Connectivity by 2D Multiple Quantum NMR , 1986 .

[15]  S. E. D. Laszlo,et al.  Total synthesis of (.+-.)-dysidin, a marine metabolite containing an N-acyl-O-methyltetramic acid , 1984 .

[16]  Willi E. Oberhänsli,et al.  Dysidin, ein neuartiger, chlorhaltiger Naturstoff aus dem Schwamm Dysidea herbacea† , 1977 .

[17]  W. A. Huffman,et al.  The Resolution of Amino Acids. II. Isoleucine, Alloisoleucine, Leucine and Norleucine1 , 1951 .

[18]  C. Willis,et al.  Three approaches to the synthesis of L-leucine selectively labelled with carbon-13 or deuterium in either diastereotopic methyl group , 2000 .

[19]  M. Garson,et al.  Cellular origin of chlorinated diketopiperazines in the dictyoceratid sponge Dysidea herbacea (Keller) , 1998, Cell and Tissue Research.

[20]  Y. Zhong,et al.  Three New Diketopiperazines from a Marine Sponge Dysidea fragilis , 1993 .

[21]  Peter Marfey,et al.  Determination ofD-amino acids. II. Use of a bifunctional reagent, 1,5-difluoro-2,4-dinitrobenzene , 1984 .

[22]  Y. Iitaka,et al.  Studies on AI-77s, microbial products with gastroprotective activity. Structures and the chemical nature of AI-77s , 1984 .

[23]  J. Buckingham.  Dictionary of organic compounds , 1982 .

[24]  W. Vetter,et al.  A novel hexachloro-metabolite from the sponge dysidea herbacea , 1977 .