Prof. Prof. Cheol-Min Park (School of Natural Science)'s work has been selected to appear on the front cover of the prestigious journal, ChemComm.
There is no rigid definition of what constitutes a suitable synthesis. The major criterion by which syntheses are judged is the potential value to the scientific community. For example, starting materials or intermediates that are useful for synthetic chemistry are appropriate. The synthesis also should represent the best available procedure, and new or improved syntheses are particularly appropriate. Syntheses of compounds that are available commercially at reasonable prices are not acceptable. We do not encourage the submission of compounds that are unreasonably hazardous, and this connection, less dangerous anions generally should be employed in place of perchlorate.
Journal of the American Chemical Society (ACS …
The five-step reaction sequence involves ring opening of a cyclic anhydride with a diamine, esterification, coupling with an amino acid isocyanide, saponification, and, finally, macro-ring closure using an Ugi or, alternatively, a Passerini multicomponent reaction.
Synthesis Information - Michigan State University
Richard Schaub, a well known psychosynthesis trainer and author, has shared two articles with us, for download, on recovering from addiction from a psychosynthetic perspective.
A synthesis is a written discussion that draws on one or more sources
It expresses the average number of weighted citations received in the selected year by the documents published in the journal in the three previous years">
Journal of Materials Synthesis and Processing - Springer
Notes by Yeomans, has generously allowed us to post a group of notes he has written on psychosynthesis topics over the years. Download the "about" pdf first for more information.
Society for Research Synthesis Methodology - Home
(Synthetic Carbohydrates Laboratory, Chemistry Department, Faculty of Science, Ain Shams University, Abbassi, 11566, Cairo, Egypt)
Current Organic Synthesis Journal Impact IF …
The attendant goal is to promote widespread acceptance of the Journal as an authoritative and indispensable holding in academic and institutional libraries.
is an open access journal of materials science and ..
An enantioselective synthesis of the indole diterpenoid natural product paspaline is disclosed. Critical to this approach was the implementation of stereoselective desymmetrization reactions to assemble key stereocenters of the molecule. The design and execution of these tactics are described in detail, and a thorough analysis of observed outcomes is presented, ultimately providing the title compound in high stereopurity. This synthesis provides a novel template for preparing key stereocenters in this family of molecules, and the reactions developed en route to paspaline present a series of new synthetic disconnections in preparing steroidal natural products.