Tag: M.W=200-250

Alkhaibari, Ibrahim S.; Kc, Hansa Raj; Roy, Subrata; Abu-gazleh, Mohd. K.; Gilmore, David F.; Alam, Mohammad A. published the artcile< Synthesis of 3,5-Bis(trifluoromethyl)phenyl-Substituted Pyrazole Derivatives as Potent Growth Inhibitors of Drug-Resistant Bacteria>, Recommanded Product: 4-Bromo-3-chloro-2-fluoroaniline, the main research area is trifluoromethyl phenyl pyrazole preparation antibacterial activity cytotoxicity SAR; Enterococcus faecalis; Enterococcus faecium; MRSA; Staphylococcus aureus; VRE; aniline; pyrazole.

The design, synthesis, and antimicrobial studies of 30 novel pyrazole derivatives I (R = C6H5, 3-FC6H4, 3,4-(F2)C6H3, etc.) have been described. Most of the synthesized compounds I are potent growth inhibitors of planktonic Gram-pos. bacteria with min. inhibitory concertation (MIC) values as low as 0.25μg/mL. Further studies led to the discovery of several lead compounds, which are bactericidal and potent against MRSA persisters. Compounds I (R = 4-BrC6H4, 3,5-(Cl)2-4-FC6H2, 4-Br-3-Cl-2-FC6H2) are potent against S. aureus biofilms with min. biofilm eradication concentration (MBEC) values as low as 1μg/mL.

Molecules published new progress about Anilines Role: RCT (Reactant), RACT (Reactant or Reagent). 115843-99-7 belongs to class bromides-buliding-blocks, and the molecular formula is C6H4BrClFN, Recommanded Product: 4-Bromo-3-chloro-2-fluoroaniline.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Parhi, Biswajit; Gurjar, Jitendra; Pramanik, Suman; Midya, Abhisek; Ghorai, Prasanta published the artcile< Correction to ""Organocatalytic Enantioselective Intramolecular Oxa-Michael Reaction of Enols: Synthesis of Chiral Isochromene"" [Erratum to document cited in CA164:592807]>, COA of Formula: C8H4BrNO, the main research area is isochromene enantioselective synthesis erratum; oxa Michael reaction enol squaramide catalyst erratum.

The structure of the catalysts used in Table 1 was omitted from the publication; A full corrected Table 1 is provided.

Journal of Organic Chemistry published new progress about Benzopyrans Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 89003-95-2 belongs to class bromides-buliding-blocks, and the molecular formula is C8H4BrNO, COA of Formula: C8H4BrNO.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Jung, Kwan-Young; Vanommeslaeghe, Kenno; Lanning, Maryanna E.; Yap, Jeremy L.; Gordon, Caryn; Wilder, Paul T.; MacKerell, Alexander D. Jr.; Fletcher, Steven published the artcile< Amphipathic α-Helix Mimetics Based on a 1,2-Diphenylacetylene Scaffold>, Name: Methyl 2-bromo-4-methoxybenzoate, the main research area is dipenylacetylene scaffold amphipathic alpha helix mimetic.

In order to mimic amphipathic α-helixes, a novel scaffold based on a 1,2-diphenylacetylene was designed. NMR and computational modeling confirmed that an intramol. hydrogen bond favors conformations of the 1,2-diphenylacetylene that allow for accurate mimicry of the i, i + 7 and i + 2, i + 5 side chains found on opposing faces of an α-helix.

Organic Letters published new progress about Amphipathicity. 17100-65-1 belongs to class bromides-buliding-blocks, and the molecular formula is C9H9BrO3, Name: Methyl 2-bromo-4-methoxybenzoate.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Tanimoto, Kouichi; Nakagawa, Naomichi; Takeda, Kazutaka; Kirihata, Mitsunori; Tanimori, Shinji published the artcile< A convenient one-pot access to phenanthridinones via Suzuki-Miyaura cross-coupling reaction>, Product Details of C8H6BrFO2, the main research area is phenanthridinone preparation Suzuki Miyaura coupling aminophenylboronic acid halobenzoate.

A convenient one-step access to biol. important phenanthridinones has been realized based upon Suzuki-Miyaura cross-coupling reaction. Reactions of 2-aminophenylboronic acid with 2-halobenzoate took place smoothly to afford substituted phenanthridinones in excellent yields in the presence of palladium(II) acetate and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (SPhos) as pre-catalysts. A natural product phenaglydon was synthesized in one-pot manner from readily available starting materials in 95% yield.

Tetrahedron Letters published new progress about Aromatic carboxylic acids, esters Role: RCT (Reactant), RACT (Reactant or Reagent). 6942-39-8 belongs to class bromides-buliding-blocks, and the molecular formula is C8H6BrFO2, Product Details of C8H6BrFO2.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Zhang, Song-Lin; Yu, Ze-Long published the artcile< Divergent synthesis of indoles, oxindoles, isocoumarins and isoquinolinones by general Pd-catalyzed retro-aldol/α-arylation>, Safety of Methyl 2-bromo-5-fluorobenzoate, the main research area is indole oxindole isocoumarin isoquinolinone preparation; aryl halide hydroxy carbonyl retro aldol arylation palladium catalyst.

Divergent synthesis of indoles I (R = H, 6-CH3, 5-F, etc.; R1 = CH3, C6H5), oxindoles II, isocoumarins e.g., III and isoquinolinones IV (R2 = CH3, C6H5) is described in this report by using a general Pd-catalyzed tandem reaction of β-hydroxy carbonyl compounds R3C(O)CH2C(R4)(OH)CH3 (R3 = CH3, C6H5, OCH3CH2; R4 = CH3, C6H5) with aryl halides bearing an ortho-nitro, -ester or -cyano substituent e.g., Me 2-chloropyridine-3-carboxylate. A key retro-aldol/α-arylation reaction is involved that merges classic Pd cross-coupling chem. with novel Pd-promoted retro-aldol C-C activation to produce α-arylated ketones or esters. Subsequent intramol. condensation of the carbonyl with the ortho-synthon gives target heterocycles I, II, e.g., III and IV. The use of common, com. available and cheap substrates and catalyst system adds addnl. synthetic advantages to the conceptual significance.

Organic & Biomolecular Chemistry published new progress about Aryl bromides Role: RCT (Reactant), RACT (Reactant or Reagent). 6942-39-8 belongs to class bromides-buliding-blocks, and the molecular formula is C8H6BrFO2, Safety of Methyl 2-bromo-5-fluorobenzoate.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Wang, Lei; Li, Sun; Chauhan, Pankaj; Hack, Daniel; Philipps, Arne R.; Puttreddy, Rakesh; Rissanen, Kari; Raabe, Gerhard; Enders, Dieter published the artcile< Asymmetric, Three-Component, One-Pot Synthesis of Spiropyrazolones and 2,5-Chromenediones from Aldol Condensation/NHC-Catalyzed Annulation Reactions>, Computed Properties of 3893-18-3, the main research area is pyrazolone enal NHC chiral aldol condensation annulation catalyst; spiropyrazolone stereoselective preparation; diketone cyclic enal NHC chiral aldol condensation annulation catalyst; chromenedione stereoselective preparation; N-heterocyclic carbene; asymmetric synthesis; chromenedione; multicomponent reaction; spiropyrazolone.

A novel one-pot, three-component diastereo- and enantioselective synthesis of spiropyrazolones has been developed involving the aldol condensation of an enal to generate α,β-unsaturated pyrazolones, which react with a second equivalent of enal through an N-heterocyclic carbene (NHC)-catalyzed [3+2] annulation. The desired spirocyclopentane pyrazolones I (R = Ph, 4-MeOC6H4, 2-MeOC6H4, 4-ClC6H4, 4-BrC6H4, 2-furanyl, 3-thienyl, etc.; R1 = t-Bu, Et, 4-MeOC6H4, 2-naphthyl; R2 = Ph, 4-MeOC6H4, 4-BrC6H4, Bn, t-Bu, etc.) are obtained in moderate to good yields and good to excellent stereoselectivities. Alternatively, starting from cyclic 1,3-diketones, 2,5-chromenediones II (R = Ph, 4-MeOC6H4, 4-MeC6H4, 4-ClC6H4, 2-MeOC6H4, etc.; R1= R2= Me, H; R1= H, R2= Ph) are available through [2+4] annulation.

Chemistry – A European Journal published new progress about Aldol condensation. 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Computed Properties of 3893-18-3.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Kuratsu, Masato; Kozaki, Masatoshi; Okada, Keiji published the artcile< 2,2':6',2'':6'',6-trioxytriphenylamine: Synthesis and properties of the radical cation and neutral species>, Reference of 135999-16-5, the main research area is trioxytriphenylamine synthesis property radical cation mol structure.

A flat radical: Oxygen-bridged triphenylamine 1 and its radical cation 2 were prepared The neutral compound has a shallow bowl structure, whereas the radical cation is planar. The properties of the highly stable radical cation were clarified; such compounds have potential applicability in electronic and magnetic materials.

Angewandte Chemie, International Edition published new progress about Crystal structure. 135999-16-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H7BrO2, Reference of 135999-16-5.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Wu, Xiaoyu; Nie, Linlin; Fang, Huihui; Chen, Jie; Cao, Weiguo; Zhao, Gang published the artcile< Organocatalyzed Cascade Reactions of Cyclic β-Enamino Esters and α,β-Unsaturated Aldehydes Leading to Indoloquinolizidines and Benzoquinolizidines>, Safety of 3-(4-Bromophenyl)acrylaldehyde, the main research area is quinolizidine fused preparation; indoloquinolizidine preparation; benzoquinolizidine preparation; organocatalyst cascade reaction cyclic enamino ester unsaturated aldehyde.

Organocatalyzed cascade reactions between cyclic β-enamino esters and α,β-unsaturated aldehydes have been developed. They provide highly substituted indolo[2,3-a]quinolizidines and benzo[a]quinolizidines in moderate to good yields and with good to excellent enantioselectivities. Both aromatic and aliphatic α,β-unsaturated aldehydes react readily with enamino esters to furnish the desired products. E.g., organocatalyzed reaction of enamino ester (I) with 4-BrC6H4CH:CHCHO gave 77% indolo[2,3-a]quinolizidine (II).

European Journal of Organic Chemistry published new progress about Cyclization (cyclic β-enamino esters). 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Safety of 3-(4-Bromophenyl)acrylaldehyde.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Riley, Robert D.; Huchenski, Blake S. N.; Bamford, Karlee L.; Speed, Alexander W. H. published the artcile< Diazaphospholene-Catalyzed Radical Reactions from Aryl Halides>, Reference of 81107-97-3, the main research area is heterocyclic compound preparation photochem; aryl halide radical cyclization diazaphospholene catalyst; Catalysis; Diazaphospholene; Heterocycles; Photochemistry; Radical Addition.

Herein, stoichiometric radical cyclizations of aryl iodides such as 1-iodo-2-[(3-phenylprop-2-en-1-yl)oxy]benzene and 1-iodo-2-[(3-methylbut-2-en-1-yl)oxy]benzene mediated by diazaphospholene hydrides are made catalytic by the combination of phenylsilane and alkali metal salts to regenerate the diazaphospholene hydride. The scope was expanded to include aryl bromides 2-Br-3-R-4-R1-5-R2C6HXR3 (X = O, S; R = H; R1 = H, F, CN, CF3, C(O)OMe; RR1 = -CH=CH-CH=CH-; R2 = H, CF3; R3 = 3-phenylbut-2-en-1-yl, 3-methylbut-2-en-1-yl, 3-phenylprop-2-en-1-yl, etc.), which benefit from visible light irradiation Twenty one substrates underwent cyclization, including a dearomative cyclization. Extension to six intermol. radical hydroarylations with arenes, thiophenes, and a pyridine e.g., 2-iodobenzotrifluoride was also accomplished.

Angewandte Chemie, International Edition published new progress about Aryl halides Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 81107-97-3 belongs to class bromides-buliding-blocks, and the molecular formula is C7H4BrF3O, Reference of 81107-97-3.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Liu, Yao-Zong; Zhang, Jie; Xu, Peng-Fei; Luo, Yong-Chun published the artcile< Organocatalytic Asymmetric Michael Addition of 1-Acetylindolin-3-ones to α,β-Unsaturated Aldehydes: Synthesis of 2-Substituted Indolin-3-ones>, COA of Formula: C9H7BrO, the main research area is indolinone enantioselective preparation; acetylindolinone unsaturated aldehyde asym Michael addition diarylprolinol trimethylsilylether catalyst.

A highly efficient asym. Michael addition of 1-acetylindolin-3-ones to α,β-unsaturated aldehydes is developed to afford 2-substituted indolin-3-one derivatives, e.g., I, in high yields (up to 94%) with good stereoselectivities (up to 11:1 dr and 96% ee). The Michael adducts can be transformed into substituted cyclopentyl[b]indoline compounds conveniently without racemization.

Journal of Organic Chemistry published new progress about Enantioselective synthesis. 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, COA of Formula: C9H7BrO.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary