The Journal of Organic Chemistry

Preparation of (R)-phenylalanine analogs by enantioselective destruction using L-amino acid oxidase

MC Pirrung, N Krishnamurthy

Index: Pirrung, Michael C.; Krishnamurthy, N. Journal of Organic Chemistry, 1993 , vol. 58, # 4 p. 957 - 958

Full Text: HTML

Citation Number: 15

Abstract

Because of the potent biological activities of naturallyoccurring amino acids and peptides and the desire for the development of therapeutics based on natural leads, methoda for preparation of unnatural amino acids have acquired great importance in medicinal chemistry.'Several of these methods are aimed specifically at the (R)-enantioniem; e acccBB to such substances provides an avenue to overcome endogenous proteolytic degradation ...

Related Articles:

Fluorinated Aromatic Amino Acids. I. o-, m-, and p-Trifluoromethylphenylalanines1

[Journal of Organic Chemistry, , vol. 25, p. 733 - 736]

Fluorinated Aromatic Amino Acids. I. o-, m-, and p-Trifluoromethylphenylalanines1

[Journal of Organic Chemistry, , vol. 25, p. 733 - 736]

Fluorinated Aromatic Amino Acids. I. o-, m-, and p-Trifluoromethylphenylalanines1

[Journal of Organic Chemistry, , vol. 25, p. 733 - 736]

Fluorinated Aromatic Amino Acids. I. o-, m-, and p-Trifluoromethylphenylalanines1

[Journal of Organic Chemistry, , vol. 25, p. 733 - 736]

Preparation of (R)-phenylalanine analogs by enantioselective destruction using L-amino acid oxidase

[Journal of Organic Chemistry, , vol. 58, # 4 p. 957 - 958]

More Articles...