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55699-10-0
4-tert-Butyl-3-hydroxy-2,6-dimethylphenylacetonitrile
55699-10-0
C₁₄H₁₉NO
217.31
White to Pale Yellow Solid
Chloroform (Sparingly), Ethyl Acetate (Slightly, Heated, Sonicated)
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文献和实验4-tert-Butyl-3-hydroxy-2,6-dimethylphenylacetonitrile
55699-10-0
C₁₄H₁₉NO
217.31
White to Pale Yellow Solid
Chloroform (Sparingly), Ethyl Acetate (Slightly, Heated, Sonicated)
Synthesis of Peptidomimetic Conjugates of Cyclic Nucleoside Phosphonates
to 200 mesh, 1% cross‐linked, typical loading 1.0 to 1.8 mmol/g; Aldrich) Methyl O‐[tert‐butyl(dimethyl)silyl]‐(L )‐serinate ( S.6 a , see protocol
Natural Product Chemistry in Action: The Synthesis of Melatonin Metabolites K1 and K2
melatonin, the kynurenamines N1-acetyl-N2 -formyl-5-methoxykynurenine (K1 ) and N -acetyl-5-methoxykynurenamine (K2 ). The four key synthetic transformations involve (a) conversion of 4-methoxy aniline into the tert -butyl (4-methoxyphenyl)carbamate, (b
Enzymes Acting on d-Amino Acid Containing Peptides
aminopeptidase and endopeptidase activities. The enzyme was active toward (d -Phe) n , Boc-(d -Phe) n , (d -Phe) n methyl ester, d -Phe-NH2 , Boc-(d -Phe) n methyl ester, and Boc-(d -Phe) n tert -butyl ester, but not toward (d -Ala) n (n = 2–4), (d
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