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. 2014 Nov 19;136(51):17738–17749. doi: 10.1021/ja510573v

Table 1. Enantioselective C–H Insertion with Diazo Ester 9a.

graphic file with name ja-2014-10573v_0019.jpg

entry catalyst solvent yield (%)a cis:trans ee, cis (%) ee, trans (%)
1 Rh2(S-PTTL)4 CH2Cl2 25 9.1:1 70 50
2 Rh2(S-PTTL)4 EtOAc trace      
3 Rh2(S-PTTL)4 hexane 34 6.7:1 51  
4 Rh2(R-PTTL)4 PhMe 47 5.9:1 −60 −33
5 Rh2(S-NTTL)4 CH2Cl2 27 9.1:1 54  
6 Rh2(S-TCPTTL)4 CH2Cl2 42   30 18
7 Rh2(R-BPTV)4 CH2Cl2 trace      
8 Rh2(S-PTTL)4 CH2Cl2c 53 10.0:1 60  
9 Rh2(S-PTAD)4 CH2Cl2c 22 3.7:1 48  
10 Rh2(R-BTPCP)4 CH2Cl2c NR      
11 Rh2(R-BPTV)4 CH2Cl2c trace      
12 Rh2(S-biTISP)2 CH2Cl2c trace 1:1    
13 Rh2(S-TCPTAD)4 CH2Cl2c 24 3:1 8  
a

Diastereomer ratios and enantiomeric excess were determined by HPLC analysis.

b

Combined isolated yield of cis-10 and trans-10.

c

At reflux.