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Tetrahedron Letters is a weekly international journal for rapid publication of full original research papers in the field of organic chemistry. According to the Journal Citation Reports , the journal has a 2022 impact factor of 1.8 [ 1 ]
Tetrahedron is a weekly peer-reviewed scientific journal covering the field of organic chemistry. According to the Journal Citation Reports, Tetrahedron has a 2020 impact factor of 2.1. [1] Tetrahedron and Elsevier, its publisher, support an annual symposium. [2] In 2010, complaints were raised over its high subscription cost. [3]
Chemical Abstracts Service Source Index Search Tool search journal titles, abbreviations, CODENs, and ISSNs Beyond CASSI compilation of historical journal abbreviations from A., B., C. to Z.; includes CASSI abbreviations used for these journals
The ACS Style is a set of standards for writing documents relating to chemistry, including a standard method of citation in academic publications, developed by the American Chemical Society (ACS).
Economics Letters; Education for Chemical Engineers; Electronic Notes in Theoretical Computer Science; Electronics Weekly; Elsevier Weekblad; Energy; Energy Economics; Energy Policy; Energy Procedia; Energy Reports; Environmental Research; eTransportation; European Journal of Cancer; European Journal of Cell Biology; European Journal of ...
Journal of Materials Chemistry A; Journal of Materials Chemistry B; Journal of Materials Chemistry C; The Journal of Neuroscience; The Journal of Physical Chemistry A; The Journal of Physical Chemistry B; The Journal of Physical Chemistry C; Journal of Physics: Condensed Matter; Journal of Physics D; Journal of the American Chemical Society
Tetrahedrane is a hypothetical platonic hydrocarbon with chemical formula C 4 H 4 and a tetrahedral structure. The molecule would be subject to considerable angle strain and has not been synthesized as of 2023.
Preparation of the trifluoromethyltrimethylsilane was reported by Ingo Ruppert in 1984. [11] In 1989, Prakash and Olah first reported activation of TMSCF 3 by fluoride to perform nucleophilic trifluoromethylation of carbonyl compounds. [12]