An Efficient Synthesis of N-tert-Butoxycarbonyl-O-cyclohexyl-L-tyrosine.-Reference-Cited by-同舟云学术

An Efficient Synthesis of N-tert-Butoxycarbonyl-O-cyclohexyl-L-tyrosine.

Published:2001 Issue:2 Volume:49 Page:233-235
ISSN:0009-2363
Container-title:Chemical and Pharmaceutical Bulletin
language:en
Short-container-title:CHEMICAL & PHARMACEUTICAL BULLETIN

Author:

NISHIYAMA Yasuhiro¹,ISHIZUKA Sou¹,SHIKAMA Suguru¹,KURITA Keisuke¹

Affiliation:

1. Department of Industrial Chemistry, Faculty of Engineering, Seikei University

Publisher

Pharmaceutical Society of Japan

Subject

Drug Discovery,General Chemistry,General Medicine

Link

http://www.jstage.jst.go.jp/article/cpb/49/2/49_2_233/_pdf

Reference9 articles.

1. 1) Present adress: Department of Pathology and Laboratory Medicine, The University of Texas-Houston Medical School, 6431 Fannin. Houston, Texas 77030, U.S.A.

2. IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). Nomenclature and symbolism for amino acids and peptides. Recommendations 1983

3. 3) Stewart J.M. “The Peptides, Vol. 3., Protection of Functional Groups in Peptide Synthesis,” ed. by Gross E., Meienhofer J., Academic Press, New York, 1981, pp.169-201.

4. Acid stability of several benzylic protecting groups used in solid-phase peptide synthesis. Rearrangement of O-benzyltyrosine to 3-benzyltyrosine

5. Protection of tyrosine in solid-phase peptide synthesis

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