K. Hewson

发表

Analogs of 6-methyl-9-beta-D-ribofuranosylpurine.

J. Montgomery, K. Hewson, 1968, Journal of medicinal chemistry.

The use of the wittig reaction in the modification of purine nucleosides

J. Montgomery, K. Hewson, A. G. Laseter, 1974 .

The preparation of 6-fluoropurines by the modified schiemann reaction

J. Montgomery, K. Hewson, 1967 .

Nucleosides of 2-fluoroadenine.

J. Montgomery, K. Hewson, 1969, Journal of medicinal chemistry.

Further Studies on the Alkylation of Purines1

J. Montgomery, S. J. Clayton, H. Thomas, 1966 .

1-Deaza-6-methylthiopurine ribonucleoside.

J. Montgomery, K. Hewson, 1966, Journal of medicinal chemistry.

3-Deaza-6-methylthiopurine Ribonucleoside1

J. Montgomery, K. Hewson, 1966 .

Derivatives of 2,5-anhydroallitol and 2,5-anhydroaltritol☆

J. Montgomery, K. Hewson, A. G. Laseter, 1973 .

A convenient method for the synthesis of 2-fluoroadenosine.

J. Montgomery, K. Hewson, 1968, The Journal of organic chemistry.

Synthesis of Potential Anticancer Agents. XX. 2-Fluoropurines2

J. Montgomery, K. Hewson, 1960 .

1-(Adenm-9-yl)-2,5-anhydro-1-deoxy-d-allitol, a homolog of adenosine

J. Montgomery, K. Hewson, 1970 .

Synthesis of potential anticancer agents. 34. Fluorobenzimidazoles and fluorobenzotriazoles.

J. Montgomery, K. Hewson, 1965, Journal of medicinal chemistry.

The Synthesis of Homoribose1

J. Montgomery, K. Hewson, 1964 .

SYNTHESIS OF POTENTIAL ANTICANCER AGENTS. X. 2-FLUOROADENOSINE1

J. Montgomery, K. Hewson, 1957 .

Synthesis of Potential Anticancer Agents. VII.2 Nucleosides Derived from L-Rhamnopyranose

B. R. Baker, K. Hewson, 1957 .

Analogs of tubercidin.

J. Montgomery, K. Hewson, 1967, Journal of medicinal chemistry.

Correlation of the Proton Magnetic Resonance Chemical Shifts of Substituted Purines with Reactivity Parameters. I. 2,6-Disubstituted Purines

J. Montgomery, W. C. Coburn, Martha C. Thorpe, 1965 .

SYNTHESIS OF POTENTIAL ANTICANCER AGENTS. XXX. (1-AZIRIDINYL)PURINES.

J. Montgomery, C. Temple, K. Hewson, 1962, Journal of medicinal and pharmaceutical chemistry.

2-Halo derivatives of 3'-acetamido-3'-deoxyadenosine.

J. Montgomery, K. Hewson, A. G. Laseter, 1975, Journal of Medicinal Chemistry.

An improved procedure for the preparation of 5-allyl-2′ -deoxyuridine

K. Hewson, John A. Montgomery and, 1965 .

Migration in the benzylation of 3-benzylhypoxanthine.

J. Montgomery, H. Thomas, K. Hewson, 1965, Chemistry and industry.

Synthesis of Potential Anticancer Agents. VI.2 Use of O-Benzoyl Blocking Group for Synthesis of 6-Chloropurine Nucleosides

H. Thomas, B. R. Baker, James A. Johnson, 1957 .

Synthesis of Potential Anticancer Agents. VIII.2Nucleosides Derived from L-Rhamnofuranose

B. R. Baker, K. Hewson, 1957 .

Epimerization in the preparation of purine nucleosides by the fusion reaction.

J. Montgomery, Martha C. Thorpe, K. Hewson, 1972, Journal of the American Chemical Society.

The 2'(3')-Phosphates of 6-Mercaptopurine Ribonucleoside and 8-Azaguanosine1

J. Montgomery, H. Thomas, K. Hewson, 1962 .

2-HALO DERIVATIVES OF 3′-ACETAMIDO-3′-DEOXYADENOSINE

J. Montgomery, K. Hewson, A. G. Laseter, 1975 .

Production, Purification, and Some Properties of Clostridium histolyticum Collagenase.∗

A. Tytell, K. Hewson, 1950, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

The synthesis of 2-bromoadenosine

J. Montgomery, K. Hewson, 1964 .

7-Substituted 7H-Purines1

J. Montgomery, K. Hewson, 1961 .