Abstract The syntheses and properties of novel, extremely strong uncharged polyaminophosphazene bases up to a high level of steric hindrance are described. Most of the systems were readily prepared in up to molar quantities and conveniently recovered from their salts. They are of appreciable to high chemical and thermal stability. Crystal structures of their salts…
Liebigs Annalen Template
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About the Liebigs Annalen format
Liebigs Annalen is a peer-reviewed journal published by Wiley, covering Asymmetric Synthesis and Catalysis, Synthetic Organic Chemistry Methods, Carbohydrate Chemistry and Synthesis.
| Publisher | Wiley |
|---|---|
| Reference style | Author–year (Chicago) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." Liebigs Annalen 12 (3): 45–58.
Formats any DOI in Liebigs Annalen style. No sign-up. |
| Publishes research in | Asymmetric Synthesis and Catalysis Synthetic Organic Chemistry Methods Carbohydrate Chemistry and Synthesis Organic Chemistry Cycloaddition Reactions Chemical Synthesis and Analysis |
| ISSN | 0947-3440 |
| h-index | 49 |
| i10-index | 583 |
| Total citations | 17,148 |
| Top institutions publishing here | University of Göttingen |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in Liebigs Annalen per year
Citation impact of Liebigs Annalen by publication year
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Most-cited papers in Liebigs Annalen
Abstract Originally reported in Liebigs Annalen in 1953 (then called Justus Liebigs Annalen der Chemie ), the Wittig reaction has evolved to include the Horner–Wittig and Horner–Wadsworth–Emmons reactions and several other variations. Today, these reactions constitute some of the most powerful processes for the construction of carbon–carbon bond frameworks, facilitating the chemical synthesis of myriads…
Abstract The synthesis, characterization and X‐ray crystallographic structure determination are described for a stable thiazol‐2‐ylidene 2 . This thiazol‐2‐ylidene is the first example of a stable, crystalline carbene in which the singlet carbene center bears a sulfur substituent. The carbene 2 is the closest stable analog of the important thiamin (vitamin B 1 ) carbene.…
Abstract More than 100 solvents and the gas phase were used to develop a solvent dipolarity‐polarizability scale that combines the medium dipolarity and polarizability into a single parameter (SPP) calculated from the UV‐visible spectra of 2‐(dimethyl‐amino)‐7‐nitrofluorene (DMANF) and its homomorph 2‐fluoro‐7‐nitrofuorene (FNF). The proposed scale compares favourably for nonprotic solvents with existing solvent polarity scales…
Abstract A total of 202 organic solvents and the gas phase were placed on a solvent basicity scale for hydrogen bond acceptor based on parameter SB. The value of such a parameter can readily be determined from the UV/Vis spectrum for an appropriate acid probe (5‐nitroindoline) (NI) and its non‐acid homomorph (1‐methyl‐5‐nitroindoline) (MNI). The proposed…