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Vogel's Textbook of Practical Organic Chemistry
Arthur I. Vogel,Brian S. Furniss +1 more
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TLDR
In this paper, the authors present a method for the synthesis of organic compounds using Spectroscopic methods and Spectral Spectral Methods (SSTM) with a focus on alicyclic and aliphatic compounds.Abstract:
1. Organic synthesis 2. Experimental techniques. 3. Spectroscopic methods. 4. Solvents and reagents. 5. Aliphatic compounds. 6. Aromatic compounds. 7. Selected alicyclic compounds. 8. Selected heterocyclic compounds. 9. Investigation and characterisation of organic compounds. 10. Physical constants of organic compounds.read more
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Chemoselective Alkylation of Thiols: A Detailed Investigation of Reactions of Thiols with Halides
TL;DR: Arylthiols, aralkylthiol and alkane thiols can be readily alkylated by alkyl/aralkyl halides in presence of K2CO3DMF to yield unsymmetrical sulphides in nearly quantitative yields as discussed by the authors.
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Simultaneous quantification of multiple nucleic acid targets using chemiluminescent probes.
TL;DR: A novel method is described for simultaneous detection and quantification of attomoles or a few femtomoles of two (or potentially more) nucleic acid targets, without need for amplification, based on spectral-temporal resolution of chemiluminescence emitted from independent hybridization-induced chemILuminescent signal probes.
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Characterization of mixed micelles of structural isomers of sodium butyl benzene sulfonate and sodium dodecyl sulfate by SANS, FTIR spectroscopy and NMR spectroscopy
TL;DR: In this article, the effect of hydrotrope concentration, hydrope structure, and temperature on the SDS micelles was studied by Small Angle Neutron Scattering (SANS), Fourier Transform Infrared (FTIR), and Nuclear Magnetic Resonance (NMR) spectroscopy for the mixed systems of SDS and NBBS.
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Synthesis, spectral, structural analysis and biological evaluation of a new hydrogen-bonded charge-transfer complex: 2,3-Dimethylquinoxalinium-p-toluenesulfonate
TL;DR: The results indicated that the compound could interact with DNA through intercalation and should have weak to moderate capacity of scavenging with DPPH, and the high thermal stability is due to the molecular frame work through H-bonding interaction.
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Structure–activity relationship of (−) mammea A/BB derivatives against Leishmania amazonensis
Mislaine Adriana Brenzan,Celso Vataru Nakamura,Benedito Prado Dias Filho,Tânia Ueda-Nakamura,Maria Claudia M. Young,Arlene G. Corrêa,Joel Alvim Júnior,Adriana Oliveira dos Santos,Diógenes Aparício Garcia Cortez +8 more
TL;DR: It is demonstrated that several aspects of the structure were important for antileishmanial activity of this coumarin, against promastigote and intracellular amastigotes of Leishmania amazonensis, and their cytotoxicity to J774G8 murine macrophages.