Alternatived Products of [ 129813-26-9 ]
Product Details of [ 129813-26-9 ]
CAS No. : | 129813-26-9 |
MDL No. : | MFCD31390411 |
Formula : |
C15H23BO2
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Boiling Point : |
- |
Linear Structure Formula : | - |
InChI Key : | - |
M.W : |
246.15
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Pubchem ID : | - |
Synonyms : |
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Safety of [ 129813-26-9 ]
Signal Word: | |
Class: | N/A |
Precautionary Statements: | |
UN#: | N/A |
Hazard Statements: | |
Packing Group: | N/A |
Application In Synthesis of [ 129813-26-9 ]
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
- Downstream synthetic route of [ 129813-26-9 ]
- 1
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[ 25015-63-8 ]
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[ 98-83-9 ]
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[ 129813-26-9 ]
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[ 280559-30-0 ]
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(E)-4,4,5,5-tetramethyl-2-(2-phenylprop-1-en-1-yl)-1,3,2-dioxaborolane
[ No CAS ]
Yield | Reaction Conditions | Operation in experiment |
0% |
In tetrahydrofuran-d8 THF-d8, room temp., 2 mol% of catalyst, 72 h; detected by NMR spectra; |
|
1: 0%
2: 0% |
In tetrahydrofuran-d8 THF-d8, room temp., 2 mol% of catalyst, 72 h; detected by NMR spectra; |
|
0% |
In tetrahydrofuran-d8 THF-d8, room temp., 2 mol% of catalyst, 72 h; detected by NMR spectra; |
|
0% |
In tetrahydrofuran-d8 THF-d8, room temp., 2 mol% of catalyst, 72 h; detected by NMR spectra; |
|
Reference:
[1]Cipot, Judy; Vogels, Christopher M.; McDonald, Robert; Westcott, Stephen A.; Stradiotto, Mark
[Organometallics, 2006, vol. 25, # 25, p. 5965 - 5968]
[2]Cipot, Judy; Vogels, Christopher M.; McDonald, Robert; Westcott, Stephen A.; Stradiotto, Mark
[Organometallics, 2006, vol. 25, # 25, p. 5965 - 5968]
[3]Cipot, Judy; Vogels, Christopher M.; McDonald, Robert; Westcott, Stephen A.; Stradiotto, Mark
[Organometallics, 2006, vol. 25, # 25, p. 5965 - 5968]
[4]Cipot, Judy; Vogels, Christopher M.; McDonald, Robert; Westcott, Stephen A.; Stradiotto, Mark
[Organometallics, 2006, vol. 25, # 25, p. 5965 - 5968]
- 2
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[ 94242-85-0 ]
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[ 145167-88-0 ]
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[ 129813-26-9 ]
- 3
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[ 25015-63-8 ]
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[ 98-83-9 ]
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[ 129813-26-9 ]
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[ 280559-30-0 ]
Yield | Reaction Conditions | Operation in experiment |
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With potassium <i>tert</i>-butylate In tetrahydrofuran at 25℃; for 5h; Inert atmosphere; Schlenk technique; Glovebox; Overall yield = 26 %Chromat.; regioselective reaction; |
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With Co((1,3-bis-(2,4,6-trimethylphenyl)imidazole-2-ylidene))<SUB>2</SUB>Cl In tetrahydrofuran at 50℃; for 6h; Inert atmosphere; Overall yield = 75 %; Overall yield = 184 mg; regioselective reaction; |
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Reference:
[1]Zhang, Guoqi; Wu, Jing; Li, Sihan; Cass, Sean; Zheng, Shengping
[Organic Letters, 2018, vol. 20, # 24, p. 7893 - 7897]
[2]Verma, Piyush Kumar; Sethulekshmi; Geetharani
[Organic Letters, 2018, vol. 20, # 24, p. 7840 - 7845]