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1-Amino- und 1,3-Diaminoimidazoliumsalze

✍ Scribed by Dr. Helmut Link; Prof. Dr. Wilhelm Klötzer; Dr. Eva Maria Karpitschka; Dr. Marc Montavon; Dr. Renate Müssner; Dr. Nicolas Singewald


Publisher
John Wiley and Sons
Year
1990
Tongue
English
Weight
230 KB
Volume
102
Category
Article
ISSN
0044-8249

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📜 SIMILAR VOLUMES


1-Amino- and 1,3-Diaminoimidazolium Salt
✍ Dr. Helmut Link; Prof. Dr. Wilhelm Klötzer; Dr. Eva Maria Karpitschka; Dr. Marc 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 251 KB 👁 1 views

The configuration of the alkylation products (e.g., 6 and 7) are fully in accord with this analysis. In summary, chiral auxiliary compounds (3) of a new shape have been described, and their action can be related to the stereoelectronics of enolate alkylations. The asymmetric environment of the auxi

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systems by the single bonds C7-N2 and C8-N1. The three nitrogen-nitrogen bonds are all shorter than the usual single N-N distance of 1.44w110.' \*I, and the N2-N4 distance is only slightly longer than the 1.24A expected for a double bond['0,''! A calculation of the best leastsquares plane passing th