15th International Symposium on the Chemistry of Natural Products, Hague, The Netherlands, 17–22 August 1986
This conference is part of the Natural Products series.
Enzymic lipoxygenation of arachidonic acid: mechanism, inhibition, and role in eicosanoid biosynthesis
Crystallographic studies of the β-lactamases from B. cereus
Use of rationally designed inhibitors to study sterol and triterpenoid biosynthesis
Bacterial organomercury lyase: a protonolytic detoxification catalyst
Progress in natural product chemistry by the chiron and related approaches - synthesis of avermectin B1a
Structure, design, and synthesis of immunoactive peptides
Developments in the chemical synthesis of naturally occurring DNA and RNA sequences with normal and unusual linkages
Synthesis and analysis of (poly)peptides
Iterative butenolide construction of polypropionate chains. Application to an efficient synthesis of (+)(9S)-dihydroerythronolide A
Synthesis of natural products using chiral glycol precursors
Vitamin B12-mediated electrochemical reactions in the synthesis of natural products
Stereoselective synthesis of β,γ-unsaturated amino acids
Generation and trapping of α-oxa and oxo o-quinodimethanes for natural product synthesis
A synthesis of moenocinol from isoprenoid precursors
Synthesis and uses of azetidiniminium salts
Synthetic studies on a stereochemically complex natural product: designs for the total synthesis of (-)-tetrodotoxin
Interaction of polyamines, their protonated salts and metal complexes with nucleic acid fragments
De novo synthesis of carbohydrates and related natural products
Switch-functionalized systems in biomimetic chemistry
Protein crystallography, computer graphics and drug design
Chemoenzymatic synthesis of a gene for the interleukin-2 receptor
Recent advances in the study of the binding site of heparin to antithrombin
Muramyl-peptides
Modification of natural products to improve their biological properties
Structure-activity relationships of cephem analogs
Penems: some recent advances
Discovery and development of new β-lactam antibiotics
Chiral control of the Staudinger reaction