M. Kotick

发表

The mRNA for a proteinase inhibitor related to the HI-30 domain of inter-α-trypsin inhibitor also encodes α-1-microgiobulin (protein HC

J. Polazzi, J. Kaumeyer, M. Kotick, 1986 .

Synthesis and properties of poly 2'-fluoro-2'-deoxyuridylic acid.

D. P. Wilson, B. Janik, R. Sommer, 1972, Biochemical and biophysical research communications.

8β-Substituted dihydrocodeinones having heteroatoms in the side chain†

J. Polazzi, M. Kotick, 1981 .

Crystal and molecular structure of 5-[1-(2′-deoxy-α-d-ribofuranosyl)uracilyl] disulfide

E. Shefter, T. Bardos, M. Kotick, 1967 .

Synthesis, cloning and expression of recombinant aprotinin.

W. Schröder, E. A. Auerswald, M. Kotick, 1987, Biological Chemistry Hoppe-Seyler.

The mRNA for a proteinase inhibitor related to the HI-30 domain of inter-alpha-trypsin inhibitor also encodes alpha-1-microglobulin (protein HC).

J. Polazzi, J. Kaumeyer, M. Kotick, 1986, Nucleic acids research.

Analgesic narcotic antagonists. 8. 7 alpha-Alkyl-4,5 alpha-epoxymorphinan-6-ones.

J. Polazzi, J. Howes, M. Kotick, 1981, Journal of medicinal chemistry.

ANALGESIC NARCOTIC ANTAGONISTS. 8. 7α-ALKYL-4,5α-EPOXYMORPHINAN-6-ONES

J. Polazzi, J. Howes, M. Kotick, 1982 .

Analgesic narcotic antagonists. 3. Preparation of 7.beta.-methyldihydrothebaine-.vphi.

J. Polazzi, M. Kotick, D. Leland, 1980 .

Analgesic narcotic antagonists. 5. 7,7-Dimethyldihydrocodeinones and 7,7-dimethyldihydromorphinones.

M. Kotick, D. Leland, 1981, Journal of medicinal chemistry.

Synthesis of 5-S-substituted 2'-deoxyuridines. Study of the factors influencing stereoselectivity of the silyl modification of the Hilbert-Johnson reaction.

C. Szántay, T. Bardos, M. Kotick, 1969, The Journal of organic chemistry.

ANALGESIC NARCOTIC ANTAGONISTS. 3. PREPARATION OF 7β-METHYLDIHYDROTHEBAINE-φ

J. Polazzi, M. Kotick, D. Leland, 1981 .

Interconversion of methyl 2,3-O-isopropylidene-β-D-ribo-and α-L-lyxo-pentofuranosiduronate methyl esters

M. Kotick, D. Leland, 1976 .

Nucleosides. 73. Ribosyl analogs of chloramphenicol.

K. Watanabe, R. Klein, J. Fox, 1971, The Journal of organic chemistry.

Studies on 4-C-(hydroxymethyl)pentofuranoses. Synthesis of 9-[4-C-(hydroxy-methyl)-α-L-threo-pentofuranosyl]adenine

M. Kotick, D. Leland, 1974 .

Rearrangement of anhydropyrimidine nucleosides in liquid hydrogen fluoride. Mechanism, scope, and synthetic studies.

J. Polazzi, M. Kotick, D. Leland, 1974, The Journal of organic chemistry.

Stereoselective synthesis of the anomeric 5-mercapto-2′-deoxyuridines and of some other α- and β-deoxyribonucleosides

C. Szántay, T. Bardos, M. Kotick, 1966 .

Nucleosides. LXXI. 3'-Amino-3'-deoxyhexopyranosyl nucleosides. VI. Reactions of some mesyloxy nucleosides.

K. Watanabe, R. J. Cushley, J. Fox, 1971, The Journal of organic chemistry.

REARRANGEMENT OF ANHYDROPYRIMIDINE NUCLEOSIDES IN LIQUID HYDROGEN FLUORIDE, MECHANISM, SCOPE, AND SYNTHETIC STUDIES

J. Polazzi, M. Kotick, D. Leland, 1975 .

Nucleosides: Part LXII. Synthetic studies on nucleoside antibiotics. 2.syntheses of methyl 4-amino-4-deoxy-d-glucosiduronic acid derivatives related to the carbohydrate moiety of gougerotin☆

R. Klein, Kyoichi A. Watanabe, J. Fox, 1969 .

Nucleosides. 63. Synthetic studies on nucleoside antibiotics. 3. Total synthesis of 1-(4-amino-4-deoxy-beta-d-glucopyranosyluronic acid)cytosine, the nucleoside moiety of gougerotin.

K. Watanabe, J. Fox, M. Kotick, 1970, The Journal of organic chemistry.

Nucleosides. LIX. Synthetic studies on nucleoside antibiotics. 1. Synthesis of 1-(4-amino-4-deoxy-beta-D-glucopyranosyl)cytosines and their identity with products derived from Gougerotin.

K. Watanabe, J. Fox, M. Kotick, 1969, Chemical & pharmaceutical bulletin.

Analgesic narcotic antagonists. 6. 7 beta, 8 beta-Methano- and 7 beta, 8 beta-epoxydihydrocodeinone.

M. Kotick, 1981, Journal of medicinal chemistry.

Analgesic narcotic antagonists. 1. 8 beta-Alkyl-, 8 beta-acyl-, and 8 beta-(tertiary alcohol)dihydrocodeinones and -dihydromorphinones.

J. Polazzi, M. Kotick, D. Leland, 1980, Journal of medicinal chemistry.