N,N-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline → Biphenyl
반응식
CC(C)(C)N=P(N1CCCC1)(N1CCCC1)N1CCCC1.CCn1c(=O)c2c(nc(N[C@@H]3CCC[C@H]3O)n2Cc2ccc(OC)c(Br)c2)n(CCO)c1=O.CN(C)c1ccc(B2OC(C)(C)C(C)(C)O2)cc1>CCC(C)(C)O.CN(C)c1ccc([PH](C(C)(C)C)(C(C)(C)C)[Pd]2([O]S(C)(=O)=O)[NH]c3ccccc3-c3cccc[c]32)cc1.CS(C)=O.O>CCn1c(=O)c2c(nc(N[C@@H]3CCC[C@H]3O)n2Cc2ccc(OC)c(-c3ccc(N(C)C)cc3)c2)n(CCO)c1=O참가 물질
10
반응물 2
생성물 3
시약·촉매·용매 5
후처리
- additionAfter 22 hours the crude reactions were diluted with 3 x 1 uL 0.5 M AcOH in DMSO (containing PhPh as an internal standard). The reactions were mixed after each dispense operation.
- aliquotMosquito(R) was used to transfer 1 uL of each quenched reaction from the 1,536-well reaction plate to 384-well analytical plates containing 60 uL DMSO for analysis.
출처 및 근거
- ORD 기록
- ord-de9cf317d2d74b3cb5147c33b1491f81
- 출처 데이터셋
- Cernak miniaturized Suzuki Cross-Coupling 12x10 Informer Library
- 원본 링크
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