Syntheses of gem-dihalocyclopropanes and their use in organic synthesis

Article Abstract:

The author reviews the publications on gem-dihalocyclopropanes. The topics of interest include the analysis of the methods used for the synthesis of these compounds, the use of the compounds as starting materials in organic chemistry, and gem-dihalocyclopropanes' applications.

Basic Chemical Manufacturing, Organic Chemicals, Organic compounds, Cyclic compounds

---

Thioamides as useful synthons in the synthesis of heterocycles

Article Abstract:

The author reviews the publications on thioamides. The topics of interest include the use of these compounds as a single building unit for the heterocyclic compound synthesis, and the synthesis of heterocycles from thioamides.

All Other Basic Organic Chemical Manufacturing, Mercaptans, Amides, Thiols

---

Heterocycles from alkylidenecyclopropanes

Article Abstract:

The authors review the publications on heterocyclic compounds. The topics of interest include the analysis of the methods used for the production of heterocyclic compounds from strained alkylidenecyclopropanes.

Italy, Science & research, Research, Chemistry, Organic, Organic chemistry

Similar abstracts:

• Abstracts: Donor-acceptor-substituted cyclopropane derivatives and their application in organic synthesis. The Heck reaction as a sharpening stone of palladium catalysis
• Abstracts: Molecularly imprinted polymers and their use in biomimetic sensors. Conjugated polymer-based chemical sensors
• Abstracts: Convergent denrons and dendrimers: from synthesis to applications. Supramolecular structures from rod-coil block copolymers
• Abstracts: Methods of ion generation. Experimental techniques in gas-phase ion thermochemistry
• Abstracts: Heavy cyclopropenes of Si, Ge, and Sn- a new challenge in the chemistry of Group 14 elements. Biomethylation of selenium and tellurium: microorganisms and plants

This website is not affiliated with document authors or copyright owners. This page is provided for informational purposes only. Unintentional errors are possible.