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. 2020 May 29;11(24):6283–6288. doi: 10.1039/d0sc01391a

Table 1. Optimization of the carboamination conditions a .

Inline graphic
Entry [Pd]/L Base Solvent/T (°C) 3/4 Yield b , c (ee) [%]
1 Pd2(dba)3/L3 NaOtBu DCM/100 5 : 1 73(47)
2 Pd2(dba)3/L3 LiOtBu DCM/100 Trace
3 Pd2(dba)3/L3 KOtBu DCM/100 Mix
4 Pd2(dba)3/L3 NaOEt DCM/100 2 : 1 52(40)
5 Pd2(dba)3/L3 NaOPh DCM/100 2 : 1 63(78)
6 Pd2(dba)3/L3 NaOPh MTBE/100 1 : 1 44(60)
7 Pd2(dba)3/L3 NaOPh 1,2-DCE/100 9 : 1 81(76)
8 Pd2(dba)3/L3 NaOPh Toluene/100 1 : 1 42(53)
9 Pd2(dba)3/L3 NaOPh MeOH/100 1 : 1 39(59)
10 Pd2(dba)3/L4 NaOPh 1,2-DCE/100 9 : 1 78(87)
11 Pd2(dba)3/L5 NaOPh 1,2-DCE/100 >30 : 1 81(93)
12 Pd2(dba)3/L6 NaOPh 1,2-DCE/100 Trace
13 Pd2(dba)3/L7 NaOPh 1,2-DCE/100 15 : 1 77(77)
14 Pd2(dba)3/L8 NaOPh 1,2-DCE/100 >30 : 1 83(93)
15 Pd(dba)2/L8 NaOPh 1,2-DCE/100 >30 : 1 79(94)
16 Pd2(dba)3·CHCl3/L8 NaOPh 1,2-DCE/100 >30 : 1 81(94)
17 Pd(OAc)2/L8 NaOPh 1,2-DCE/100 >30 : 1 74(94)
18 3-C3H5)2Pd2Cl2/L8 NaOPh 1,2-DCE/100 >30 : 1 69(94)
19 Pd A/L8 NaOPh 1,2-DCE/100 >30 : 1 82(94)
20 Pd A/L8 NaOPh 1,2-DCE/80 >30 : 1 81(93)
21 Pd A/L8 NaOPh 1,2-DCE/50 >30 : 1 81(95)
22 Pd A/L8 NaOPh 1,2-DCE/20 >30 : 1 84(96)
23 d Pd A/L8 NaOPh 1,2-DCE/20 >30 : 1 79(96)

aUnless otherwise specified, all reactions were carried out with 1a (0.2 mmol), 2a (0.8 mmol, 4 eq.), a [Pd] source (0.01 mmol, 5 mol%), N-Me-Xiang-phos (0.024 mmol, 12 mol%), base (0.8 mmol, 4 eq.), and H2O (7.2 μL, 2 eq.) in a solvent (1 mL, 0.2 M).

bYield of isolated product 3aa.

cDetermined by chiral HPLC.

d2 eq. H2O were removed.