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(Benzylamine) trifluoroboron, inozivikanwawo seBnNH2 · BF3, inokosha reagent mu organic synthesis uye catalysis.Iyo yakaoma yakaumbwa pakati pe benzylamine ne boron trifluoride (BF3).Heino tsananguro yekushandiswa kwayo mumashoko angangoita 300. Imwe yekushandiswa kwekutanga kwe (benzylamine) trifluoroboron iri mumunda weCN bond formation.Inogona kushandiswa sechinhu chinokonzeresa muakasiyana-siyana ekubatanidza maitiro, kunyanya mukuumbwa kweCN bond.Aya maitiro akakosha mukugadzirwa kwemishonga, agrochemicals, uye mamwe makemikari akanaka.Iyo (benzylamine) trifluoroboron yakaoma inoita seyakatangira yepakati inoshanda inobatsira mukubatanidza nucleophiles nearyl kana alkyl halides, zvichiita kuti kuumbwa kwecarbon-nitrogen bond.Iyi CN bond formation yakakosha mukugadzira ma organic molecules ane anodiwa maumbirwo uye anoshanda zvivakwa.Kumwe kushanda kwakakosha kwe (benzylamine) trifluoroboron kuri mumunda wepeptide neprotein synthesis.Inoshandiswa seboka rinodzivirira remamines mune yakasimba-chikamu peptide synthesis uye yekuzvarwa makemikari ligation.Iyo (benzylamine) trifluoroboron yakaoma inoshanda seboka rinobvisika rinodzivirira rinogona kutsemurwa zviri nyore pasi pemamiriro akapfava.Inopa kuchengetedzwa kwakavimbika kune amine inoshanda boka panguva dzakasiyana siyana dzemakemikari manipulations ichiramba yakagadzikana panguva yepeptide synthesis.Kana kuumbwa kwapera, boka rinodzivirira rinogona kubviswa nyore nyore, richibvumira chizvarwa chekuzvarwa peptide kana mapuroteni maitiro.Uyezve, (benzylamine) trifluoroboron inowana kushandiswa mumunda weasymmetric synthesis.Inogona kushandiswa se organocatalyst mune dzakasiyana-siyana enantioselective shanduko.Nekuda kwehunhu hwayo hwechiral, iyo (benzylamine) trifluoroboron yakaoma inogona kukonzeresa stereochemistry panguva yekuita, zvichitungamira mukuumbwa kwezvigadzirwa zvakachena.Inogona kushandiswa mukuita senge asymmetric aldol reactions, Mannich reactions, acylations, uye mamwe kabhoni-kabhoni uye kabhoni-nitrogen bond-forming maitiro.The organocatalytic properties ye (benzylamine) trifluoroboron inoita kuti ive chinhu chakakosha mukugadzirwa kwechiral intermediates uye inoshingaira mishonga yemishonga.Uyezve, (benzylamine) trifluoroboron inogona kushandiswa mukubatanidza chemistry uye zvinhu zvesayenzi.Inogona kushanda sechivakwa mukubatanidzwa kwesimbi-organic frameworks (MOFs), coordination complexes, uye zvimwe zvinoshanda.Iko kurongeka kwe (benzylamine) trifluoroboron ine simbi ions inopa kugadzikana uye kugarika kune izvi zvinhu, zvichipesvedzera hunhu hwazvo, makemikari, uye catalytic.Kugona kubatanidza (benzylamine) trifluoroboron mune izvi zvinhu kunovhura mikana yekugadzirwa nekuvandudzwa kwezvinhu zvitsva zvine maapplication mu catalysis, kuchengetedza gasi, kupatsanura, uye kunzwa. organic synthesis uye catalysis.Kushandiswa kwayo muCN bond formation, peptide uye protein synthesis, asymmetric synthesis, uye coordination chemistry inosimbisa kukosha kwayo mune dzakasiyana siyana.Iyo (benzylamine) trifluoroboron yakaoma inopa yakakwidziridzwa reactivity uye kusarudza, inogonesa kusanganiswa kweakaoma organic mamorekuru, chiral makomisheni, uye zvinoshanda zvinhu.Hunhu hwayo hwakakosha hunoita kuti ive chishandiso chakakosha kune vanoongorora muzvidzidzo uye indasitiri inoshanda yakanangana nekugadzirwa kwemakemikari matsva, mishonga, uye zvinhu.