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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
216319-90-3

Boc-L-Val-nitrile synthesis

5synthesis methods
35150-08-4 Synthesis
BOC-VAL-NH2

35150-08-4
82 suppliers
$11.00/250mg

Boc-L-Val-nitrile

216319-90-3
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Yield:216319-90-3 86%

Reaction Conditions:

with pyridine;trifluoroacetic anhydride in tetrahydrofuran at -10 - 0; for 2 h;

References:

Sureshbabu, Vommina V.;Naik, Shankar A.;Nagendra [Synthetic Communications,2009,vol. 39,# 3,p. 395 - 406] Location in patent:experimental part

N-Boc-L-valine

13734-41-3
548 suppliers
$8.00/1g

Boc-L-Val-nitrile

216319-90-3
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References
72-18-4 Synthesis
L-Valine

72-18-4
833 suppliers
$5.00/25g

Boc-L-Val-nitrile

216319-90-3
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References
24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
834 suppliers
$13.50/25G

Boc-L-Val-nitrile

216319-90-3
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References
L-Valine, N-[(1,1-dimethylethoxy)carbonyl]-, anhydride with ethyl hydrogen carbonate (9CI)

98807-40-0
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Boc-L-Val-nitrile

216319-90-3
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References

Boc-L-Val-nitrile Related Search:

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