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. 2022 May 16;61(38):e202204535. doi: 10.1002/anie.202204535

Table 1.

Exploration of reaction conditions.

graphic file with name ANIE-61-0-g003.jpg

Entry

Variation from “standard condtions”[a]

Yield [%][b]

1

None

85

2

Pd(OAc)2

70

3

Si i Pr3‐protected bromoalkyne (3′)

<5

4

t BuO2C‐ instead of PA (1a′)

<5

5

1a′, 3′

<5

6

1a′, Pd(dba)2, DPE‐Phos, NaOtBu, PhMe

<5

7

1a′, 3′, Pd(dba)2, DPE‐Phos, NaOtBu, PhMe

<5

[a] Reactions conducted using 0.1 mmol 1a at 0.1 M. [b] Yield determined by 1H NMR analysis of unpurified reaction mixture. DPE‐Phos=Bis[(2‐diphenylphosphino)phenyl] ether.