Tag: M.W=50-100

Steiman, Talia J. published the artcileSynthesis of β-Phenethylamines via Ni/Photoredox Cross-Electrophile Coupling of Aliphatic Aziridines and Aryl Iodides, Recommanded Product: 2-Aminobutan-1-ol, the publication is Journal of the American Chemical Society (2020), 142(16), 7598-7605, database is CAplus and MEDLINE.

A photoassisted Ni-catalyzed reductive cross-coupling between tosyl-protected alkyl aziridines and com. available (hetero)aryl iodides is reported. This mild and modular method proceeds in the absence of stoichiometric heterogeneous reductants and uses an inexpensive organic photocatalyst to access medicinally valuable β-phenethylamine derivatives Unprecedented reactivity was achieved with the activation of cyclic aziridines. Mechanistic studies suggest that the regioselectivity and reactivity observed under these conditions are a result of nucleophilic iodide ring opening of the aziridine to generate an iodoamine as the active electrophile. This strategy also enables cross-coupling with Boc-protected aziridines.

Journal of the American Chemical Society published new progress about 96-20-8. 96-20-8 belongs to alcohols-buliding-blocks, auxiliary class Amine,Aliphatic hydrocarbon chain,Alcohol, name is 2-Aminobutan-1-ol, and the molecular formula is C7H7ClN2S, Recommanded Product: 2-Aminobutan-1-ol.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

Zhang, Chong published the artcileMultiple Responsive CPL Switches in an Enantiomeric Pair of Perovskite Confined in Lanthanide MOFs, Application In Synthesis of 96-20-8, the publication is Advanced Materials (Weinheim, Germany) (2022), 34(11), 2109496, database is CAplus and MEDLINE.

Circularly polarized luminescence (CPL) switches have attracted widespread attention due to their potential applications in advanced information technologies. However, the design and fabrication of solid-state multiple-responsive CPL switches remain challenging. Here, through self-assembly of chiral metal-organic frameworks (MOFs) and perovskite nanocrystals (NCs), a pair of crystalline enantiomeric (P)-(+)/(M)-(-)-EuMOF⊃MAPbX3 (MA = CH3NH3+, X = Cl-, Br-, I-) adducts is prepared, where the achiral MAPbBr3 perovskite NCs embedded into chiral MOFs inherit the chirality of host MOFs by host-guest EuBr and PbO coordination bonds, which is demonstrated by synchrotron-radiation-based X-ray absorption spectroscopy. The chiral adducts show enhanced photoluminescence quantum yield (PLQY), good thermal stability of CPL in air, and photoswitchable CPL properties upon altering different UV irradiation Based on two chiral emission centers and their different characteristics, reversible CPL switches are realized upon a diversity of external stimuli, for example, chems. (water /CH3NH3Br solution) or temperatures (room temperature/high temperature). Benefiting from the extraordinary stimuli-responsive and highly reversible switchable CPL, multiple information encryptions and decryptions integrated with CPL, together with a chiroptical logic gate are successfully designed. This work opens a new avenue to generally fabricate solid-state CPL composite materials and develops new applications based on switchable CPL.

Advanced Materials (Weinheim, Germany) published new progress about 96-20-8. 96-20-8 belongs to alcohols-buliding-blocks, auxiliary class Amine,Aliphatic hydrocarbon chain,Alcohol, name is 2-Aminobutan-1-ol, and the molecular formula is C9H7NO4, Application In Synthesis of 96-20-8.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

Wang, Gang published the artcileLiquid-Phase Epoxidation of Propylene with H₂O₂ over TS-1 Zeolite: Impurity Formation and Inhibition Study, Safety of 2-Aminobutan-1-ol, the publication is Industrial & Engineering Chemistry Research (2021), 60(32), 12109-12122, database is CAplus.

The liquid-phase epoxidation of propylene with H₂O₂ over titanium silicalite-1 (TS-1) zeolite was investigated in detail with a focus on the formation and inhibition of various trace impurities like acetaldehyde, propionaldehyde, acetone, hydroxyacetone, acetals, esters, etc. The results showed that the formation of trace impurities involved the transformation of propylene oxide (PO), its oxidation/isomerization/ring-opening (solvolysis and hydrolysis) byproducts, methanol solvent, and even propylene. Roughly speaking, the epoxidation conditions, viz., low temperature, short residence time, and slightly alk. reaction medium, that are beneficial to suppress the ring-opening byproducts of PO, were seen facilitating the inhibition of trace impurities as well. To lower the trace impurities via modification of the TS-1 catalyst, the hydrothermal modification of TS-1 with organic amines such as amino-2-propanol (MIPA) was attempted and its effectiveness was demonstrated. The TS-1 zeolite suitably modified by MIPA exhibited abundant Ti-OH groups (3672 cm^-1) together with remarkably decreased PO adsorption.

Industrial & Engineering Chemistry Research published new progress about 96-20-8. 96-20-8 belongs to alcohols-buliding-blocks, auxiliary class Amine,Aliphatic hydrocarbon chain,Alcohol, name is 2-Aminobutan-1-ol, and the molecular formula is C5H10O, Safety of 2-Aminobutan-1-ol.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

He, Yu-Tao published the artcileSynthesis of Various Bridged Ring Systems via Rhodium-Catalyzed Bridged (3+2) Cycloadditions, Name: (R)-Oxiran-2-ylmethanol, the publication is Organic Letters (2022), 24(1), 186-190, database is CAplus and MEDLINE.

Here, the authors describe the rhodium-catalyzed bridged [3+2]-cycloaddition cascade reactions of N-sulfonyl-1,2,3-triazoles, which allowed the efficient diastereoselective construction of various functionalized and synthetically challenging bridged ring systems. This simple, direct transformation had a broad substrate scope and excellent functional group tolerance. The highly strained polycyclic bicyclo[2.2.2]octa[b]indole core of fruticosine was synthesized efficiently using this methodol.

Organic Letters published new progress about 57044-25-4. 57044-25-4 belongs to alcohols-buliding-blocks, auxiliary class Epoxides,Chiral,Aliphatic hydrocarbon chain,Alcohol, name is (R)-Oxiran-2-ylmethanol, and the molecular formula is C3H6O2, Name: (R)-Oxiran-2-ylmethanol.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

Yue, Rong published the artcileInsight into enzyme-catalyzed aziridine formation mechanism in ficellomycin biosynthesis, Safety of 2-Aminobutan-1-ol, the publication is European Journal of Medicinal Chemistry (2020), 112639, database is CAplus and MEDLINE.

Ficellomycin is an aziridine-containing antibiotic, produced by Streptomyces ficellus. Based on the newly identified ficellomycin gene cluster and the assigned functions of its genes, a possible pathway for aziridine ring formation in ficellomycin was proposed, which is a complex process involving at least 3 enzymic steps. To obtain support for the proposed mechanism, the targeted genes encoding sulfate adenylyltransferase, adenylsulfate kinase, and a putative sulfotransferase were resp. disrupted and the subsequent anal. of their fermentation products revealed that all the three genes were involved in aziridine formation. To further confirm the mechanism, the key gene encoding a putative sulfotransferase was over expressed in Escherichia coli Rosseta (DE3). Enzyme assays indicated that the expressed sulfotransferase could specifically transfer a sulfo group from 3′-phosphoadenosine-5′-phosphosulfate (PAPS) onto the hydroxyl group of (R)-(-)-2-pyrrolidinemethanol. This introduces a good leaving group in the form of the sulfated hydroxyl moiety, which is then converted into an aziridine ring through an intramol. nucleophilic attack by the adjacent secondary amine. The sulfation/intramol. cyclization reaction sequence maybe a general strategy for aziridine biosynthesis in microorganisms. Discovery of this mechanism revealed an enzyme-catalyzed route for the synthesis of aziridine-containing reagents and provided an important insight into the functional diversity of sulfotransferases.

European Journal of Medicinal Chemistry published new progress about 96-20-8. 96-20-8 belongs to alcohols-buliding-blocks, auxiliary class Amine,Aliphatic hydrocarbon chain,Alcohol, name is 2-Aminobutan-1-ol, and the molecular formula is C5H6N2O2, Safety of 2-Aminobutan-1-ol.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

Ho, Steven Sai Hang published the artcileSeasonal behavior of water-soluble organic nitrogen in fine particulate matter (PM_2.5) at urban coastal environments in Hong Kong, Quality Control of 96-20-8, the publication is Air Quality, Atmosphere & Health (2019), 12(4), 389-399, database is CAplus.

Water-soluble organic nitrogen (WSON) in fine particulate matter (PM_2.5) was determined at urban coastal environments in China based on 1-yr measurement. The WSON concentrations were in a range of 14.3-257.6 nmol N m^-3 and accounted for 22.0-61.2% of the water-soluble nitrogen (WSN) in composition The average total concentration of free amino acid (FAA) was 1264.5 ± 393.0 pmol m^-3, which was lower than those in continental urban cities but nevertheless comparable to the rural area of Pearl River Delta (PRD) in China. The total quantified amines and amino compounds ranged from 223.8 to 806.0 pmol m^-3 in which methylamine, ethylamine, and ethanolamine were the most abundant compounds The average concentration of urea was 7.8 ± 3.0 nmol m^-3 and at least one order of magnitude higher than those in marine and rural areas but comparable to other continental cities in China during non-dust period. Summer showed the highest average concentration of WSON (95.0 ± 66.6 nmol N m^-3) and composition in WSN (49.3%) compared to other seasons (27.9-37.0%). The results were consistent with previous findings that the inorganics can contribute more than the organics in secondary aerosol formation. There were no distinctive seasonal variations of organic compositions of FAA, amine and amino compounds, and urea. This observation was possibly attributed to a mix of original sources in urban and different prevailing wind directions. Fair correlations (r < 0.4) between WSON compounds and atm. oxidants [ozone (O₃) and nitrogen oxides (NO_x)] suggest that biogenic oxidation is possibly not a major contributing factor in atm. coastal urban location.

Air Quality, Atmosphere & Health published new progress about 96-20-8. 96-20-8 belongs to alcohols-buliding-blocks, auxiliary class Amine,Aliphatic hydrocarbon chain,Alcohol, name is 2-Aminobutan-1-ol, and the molecular formula is C4H11NO, Quality Control of 96-20-8.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

Gerard, Baudouin published the artcileSynthesis of Stereochemically and Skeletally Diverse Fused Ring Systems from Functionalized C-Glycosides, Category: alcohols-buliding-blocks, the publication is Journal of Organic Chemistry (2013), 78(11), 5160-5171, database is CAplus and MEDLINE.

A diversity-oriented synthesis (DOS) strategy was developed for the synthesis of stereochem. diverse fused-ring systems containing a pyran moiety. Each scaffold contains an amine and Me ester for further diversification via amine capping and amide coupling. Scaffold diversity was evaluated in comparison to previously prepared scaffolds by a shape-based principal moments of inertia (PMI) anal.

Journal of Organic Chemistry published new progress about 57044-25-4. 57044-25-4 belongs to alcohols-buliding-blocks, auxiliary class Epoxides,Chiral,Aliphatic hydrocarbon chain,Alcohol, name is (R)-Oxiran-2-ylmethanol, and the molecular formula is C3H6O2, Category: alcohols-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

Bolli, Martin H. published the artcileNovel S1P₁ receptor agonists – Part 5: From amino-to alkoxy-pyridines, Related Products of alcohols-buliding-blocks, the publication is European Journal of Medicinal Chemistry (2016), 326-341, database is CAplus and MEDLINE.

In a previous communication we reported on the discovery of aminopyridine 1 as a potent, selective and orally active S1P₁ receptor agonist. More detailed studies revealed that this compound is phototoxic in vitro. As a result of efforts aiming at eliminating this undesired property, a series of alkoxy substituted pyridine derivatives was discovered. The photo irritancy factor (PIF) of these alkoxy pyridines was significantly lower than the one of aminopyridine 1 and most compounds were not phototoxic. Focused SAR studies showed, that 2-, 3-, and 4-pyridine derivatives delivered highly potent S1P₁ receptor agonists. While the 2-pyridines were clearly more selective against S1PR₃, the corresponding 3- or 4-pyridine analogs showed significantly longer oral half-lives and as a consequence longer pharmacol. duration of action after oral administration. One of the best compounds, cyclopentoxy-pyridine 45b lacked phototoxicity, showed EC₅₀ values of 0.7 and 140 nM on S1PR₁ and S1PR₃, resp., and maximally reduced the blood lymphocyte count for at least 24 h after oral administration of 10 mg/kg to Wistar rats.

European Journal of Medicinal Chemistry published new progress about 57044-25-4. 57044-25-4 belongs to alcohols-buliding-blocks, auxiliary class Epoxides,Chiral,Aliphatic hydrocarbon chain,Alcohol, name is (R)-Oxiran-2-ylmethanol, and the molecular formula is C3H6O2, Related Products of alcohols-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

Zhang, Qiao published the artcileSynthesis and photoluminescence of organotin-dithiothreitol clusters, Recommanded Product: 2-Aminobutan-1-ol, the publication is Journal of Solid State Chemistry (2021), 122056, database is CAplus.

Three novel organotin oxysulfide hybrid clusters (BuSn)₄(DTT)₄M (M = Sn⁴⁺ (1), Ti⁴⁺ (2), Hf⁴⁺ (3); DTT = 1,4-dithiothreitol) were prepared by hydrothermal methods and their crystal structures were determined by single-crystal X-ray diffraction. These clusters are isostructural, pentanuclear complexes containing four peripheral butyltin fragments, and a central metal site of either tin, titanium or hafnium. Solid state variable temperature fluorescence spectra showed that the position and the intensity of key emission peaks of the three isomorphic compounds are significantly different. Compound 1 gave bimodal emission at 420 and 445 nm upon excitation at 360 nm, and its peak positions remained unchanged. Compounds 2 and 3 were excited by 365 and 460 nm radiation, resp., and their maximum emission peaks were red-shifted in different degrees with decreasing temperature All their peak intensity increased with decreasing temperature Solid-state UV/visible diffuse reflectance spectra displayed that these three isostructural compounds have wide optical band gaps of 3.72, 2.68, and 3.19 eV, resp.

Journal of Solid State Chemistry published new progress about 96-20-8. 96-20-8 belongs to alcohols-buliding-blocks, auxiliary class Amine,Aliphatic hydrocarbon chain,Alcohol, name is 2-Aminobutan-1-ol, and the molecular formula is C26H41N5O7S, Recommanded Product: 2-Aminobutan-1-ol.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts

Shirbhate, Mukesh Eknath published the artcileOptical and Fluorescent Dual Sensing of Aminoalcohols by in Situ Generation of BODIPY-like Chromophore, Related Products of alcohols-buliding-blocks, the publication is Journal of the American Chemical Society (2020), 142(11), 4975-4979, database is CAplus and MEDLINE.

A novel multifunctional aminophenylboronic acid connected to a diphenylketone gives both CD and fluorescence signals by in situ generation of a BODIPY-like chromophore in the presence of aminoalcs. DFT calculations were used to understand the role of each functional group in the mechanism. This new sensor can distinguish different aminoalcs. and quant. indicate the concentration of the substrate, allowing for the convenient determination of the ee of racemic mixtures with a single probe.

Journal of the American Chemical Society published new progress about 96-20-8. 96-20-8 belongs to alcohols-buliding-blocks, auxiliary class Amine,Aliphatic hydrocarbon chain,Alcohol, name is 2-Aminobutan-1-ol, and the molecular formula is C7H7IN2O, Related Products of alcohols-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Alcohol,
Alcohols – Chemistry LibreTexts