추천 제품
분석
≥95%
양식
powder or crystals
mp
144-160 °C
SMILES string
FC(F)(F)c1cc(cc(c1)C(F)(F)F)NC(=O)N(C(C)C)c2c(c6c(cc2)cccc6)c3c4c(ccc3NC(=O)Nc5cc(cc(c5)C(F)(F)F)C(F)(F)F)cccc4
InChI
1S/C41H28F12N4O2/c1-21(2)57(37(59)55-29-19-26(40(48,49)50)16-27(20-29)41(51,52)53)33-14-12-23-8-4-6-10-31(23)35(33)34-30-9-5-3-7-22(30)11-13-32(34)56-36(58)54-28-17-24(38(42,43)44)15-25(18-28)39(45,46)47/h3-21H,1-2H3,(H,55,59)(H2,54,56,58)
애플리케이션
((S)-3-(3,5-Bis(trifluoromethyl)phenyl)-1-(2′-(3-(3,5-bis(trifluoromethyl)phenyl)ureido)-[1,1′-binaphthalen]-2-yl)-1-isopropylurea is a hydrogen bonding phase-transfer catalyst capable of activating CsF for the asymmetric nucleophilic fluorination of sulfoniums.1
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
Science (New York, N.Y.), 360(6389), 638-642 (2018-05-12)
Common anionic nucleophiles such as those derived from inorganic salts have not been used for enantioselective catalysis because of their insolubility. Here, we report that merging hydrogen bonding and phase-transfer catalysis provides an effective mode of activation for nucleophiles that
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