W. Anderson

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A Simplified Procedure for the Efficient Conversion of Aromatic Aldehydes into Esters

G. Lai, W. Anderson, 1997 .

Antitumor activity and cross-resistance of carmethizole hydrochloride in preclinical models in mice

J. Plowman, W. Waud, D. Dykes, 2004, Cancer Chemotherapy and Pharmacology.

Synthesis, molecular modeling, and evaluation of nonphenolic indole analogs of mycophenolic acid.

R. Bernacki, G. Makara, P. Pera, 2004, Bioorganic & medicinal chemistry.

Synthesis of 3,9b‐dihydro‐5H‐pyrrolo[2,1‐a]isoindoles and 3,5,6,10b‐tetrahydropyrrolo[2,1‐a]isoquinolines with 1,3‐dipolar cycloaddition reactions

F. R. Kinder, W. Anderson, 1990 .

Synthesis, chemical reactivity, and antitumor evaluation of congeners of carmethizole hydrochloride, an experimental "acylated vinylogous carbinolamine" tumor inhibitor.

M. Jarosinski, W. Anderson, P. S. Reddy, 1993, Journal of medicinal chemistry.

Synthesis and evaluation of furan, thiophene, and azole bis[(carbamoyloxy)methyl] derivatives as potential antineoplastic agents.

W. Anderson, A. Jones, 1984, Journal of medicinal chemistry.

BORON TRIFLUORIDE-DIETHYL ETHER COMPLEX CATALYZED AROMATIC AMINO-CLAISEN REARRANGEMENTS

G. Lai, W. Anderson, 1995 .

Synthesis, chemistry, and antineoplastic activity of alpha-halopyridinium salts: potential pyridone prodrugs of acylated vinylogous carbinolamine tumor inhibitors.

D. Dean, W. Anderson, T. Endo, 1990, Journal of medicinal chemistry.

The synthesis of polycyclic benz-fused pyrroles†

W. Anderson, Howard L. Mcpherson Jr. and, N. J. Stewart, 1980 .

Synthesis and antileukemic activity of bis[[(carbamoyl)oxy]methyl]- substituted pyrrolo[2,1-a]isoquinolines, pyrrolo[1,2-a]quinolines, pyrrolo[2,1-a]isobenzazepines, and pyrrolo[1,2-a]benzazepines.

N. Raju, W. Anderson, A. Heider, 1988, Journal of medicinal chemistry.

Synthesis and structure-activity relationship studies of cytotoxic epoxide derivatives of 7-oxabicyclo[2.2.1]heptane.

W. Anderson, R. Dewey, 1977, Journal of medicinal chemistry.

1,3-Dipolar cycloaddition reactions with tetrafluoroborate and trifluoromethanesulfonate salts of 1,2-dihydro- and 1,2,3,4-tetrahydroquinoline Reissert compounds

W. Anderson, A. Heider, J. D. Ruiter, 1985 .

Synthesis of Novel Indole Analogues of Mycophenolic Acid as Potential Antineoplastic Agents

G. Lai, W. Anderson, 2000 .

Design, synthesis, antineoplastic activity, and chemical properties of bis(carbamate) derivatives of 4,5-bis(hydroxymethyl)imidazole.

D. Bhattacharjee, W. Anderson, D. Houston, 1989, Journal of medicinal chemistry.

Nuclear magnetic resonance and molecular modeling study on mycophenolic acid: implications for binding to inosine monophosphate dehydrogenase.

G. Keserű, G. Makara, M. Kajtár-Peredy, 1996, Journal of medicinal chemistry.

A Simple Efficient Synthesis of 5,8-Isoquinolinedione

W. Anderson, B. P. Connarty, Toni El-hajj, 1986 .

A retro Diels-Alder synthesis of 3-pyrrolines

W. Anderson, A. S. Milowsky, 1985 .

Synthesis, antitumor activity, and chemical properties of silaplatin and related platinum (II) and platinum (IV) complexes derived from beta-silyl amines.

J. Plowman, V. Narayanan, R. Haugwitz, 1995, Journal of medicinal chemistry.

Synthesis of 2-methylbenzo[b]furans and 2-methylbenzo[b]thiophens

E. LaVoie, W. Anderson, 1974 .

Use of 2,3-dichloropropene and 1,3-dichlorobut-2-ene as synthons for heterocyclic compounds: synthesis of 2-methylbenzo[b]furans, 2-methylbenzo[b]thiophens, and 4-methyl-2H-chromen

E. LaVoie, J. Bottaro, W. Anderson, 1976 .

Facile acyl migration in 6-O-acylcastanospermine

A. Gopalsamy, W. Anderson, 1991 .

A Simple Efficient Synthesis of 3-Pyrrolines Using A 1,3-Dipolar Cycloadoition Reaction with An Ylioe Generated by Thermal Desilylation of An α-Silylimminium Salt

T. T. Dabrah, W. Anderson, 1986 .

Synthesis of 4-(2-chloroethyl)-2,3-dihydro[1,4]oxazino[2,3- b ]quinoline and 4-(2-chloroethyl)2,3-dihydropyrido[2,3- b ][1,4]oxazine

D. Dalvie, W. Anderson, 1993 .

Synthesis and antileukemic activity of 1-methyl-2,5-diphenyl-3,4-bis(hydroxymethyl)-, 1,2,3-triphenyl-4,5-bis(hydroxymethyl)-, and 1-methyl-2,3-diphenyl-4,5-bis(hydroxymethyl)pyrrole bis(N-methylcarbamate).

M. J. Halat, W. Anderson, A. C. Rick, 1980, Journal of medicinal chemistry.

Synthesis of erbstatin, a naturally occurring inhibitor of tyrosine-specific protein kinase

T. T. Dabrah, W. Anderson, D. Houston, 1987 .

Synthesis, chemical reactivity, and antileukemic activity of 5-substituted 6,7-bis(hydroxymethyl)pyrrolo[1,2-c]thiazole biscarbamates and the corresponding sulfoxides and sulfones.

R. Mach, W. Anderson, 1987, Journal of Medicinal Chemistry.

Synthesis and chemical reactivity of c-5 substituted 6,7-bis-(hydroxymethyl)-1H-pyrrolizine biscarbamate tumor inhibitors †

R. Mach, W. Anderson, 1990 .

Vinylogous Carbinolamine Tumor Inhibitors. Part 21. Synthesis, Chemical Reactivity, and Antileukemic Activity of 5-Substituted 6,7-Bis(hydroxymethyl)pyrrolo(1,2-c)thiazole Biscarbamates and the Corresponding Sulfoxides and Sulfones.

R. Mach, W. Anderson, 1988 .

A simple procedure for the epoxidation of acid-sensitive olefinic compounds with m-chloroperbenzoic acid in an alkaline biphasic solvent system.

W K Anderson, T Veysoglu, W. Anderson, 1973, The Journal of organic chemistry.

3-Pyrroline N-oxide bis(carbamate) tumor inhibitors as analogues of indicine N-oxide.

W. Anderson, A. S. Milowsky, 1987, Journal of medicinal chemistry.

Oxidative Degradation of Castanospermine

W. Anderson, P. Tan, 1994 .

Oxidative Degradation of Castanospermine.

W. Anderson, P. Tan, 1995 .

A facile selective acylation of castanospermine

A. Gopalsamy, T. Howe, R. A. Coburn, 1990 .

A Facile Selective Acylation of Castanospermine.

A. Gopalsamy, T. Howe, R. A. Coburn, 1990 .

Chloroacetylation of 1-Azaphenothiazine

J. Steele, W. Anderson, W. Tracer, 1972 .

The Use of N-Ethyl-N'-Dimethylamincfropylcarbodiimide or Silicon Tetrachloride in Pyrrole Syntheses

W. Anderson, A. Heider, 1986 .

Synthesis of 3-pyrrolines by an intramolecular wittig reaction

M. Jarosinski, F. R. Kinder, W. Anderson, 1991 .

Antileukemic activity of derivatives of 1-phenyl-2,5-dimethyl-3,4-bis(hydroxymethyl)pyrrole bis(N-methylcarbamate).

W. Anderson, P. Corey, 1977, Journal of medicinal chemistry.

Synthesis and antileukemic activity of 5-substituted 2,3-dihydro-6,7-bis(hydroxymethyl)-1H-pyrrolizine diesters.

W. Anderson, P. Corey, 1977, Journal of medicinal chemistry.

Synthesis of 3-Pyrrolines by an Intramolecular Wittig Reaction.

M. Jarosinski, F. R. Kinder, W. Anderson, 1992 .

Synthesis of Methyl 2,3-bis(hydroxymethyl)-5-phenyl-7-oxabicyclo[2.2.1]hepta-2,5-diene- 6-carboxylate bis(N-methylcarbamate) derivatives as potential antitumor agents.

W. Anderson, B. Mulumba, 1984, Journal of Pharmacy and Science.

Activity of bis-carbamoyloxymethyl derivatives of pyrroles and pyrrolizines against human tumor xenografts in nude mice.

W. Anderson, 1982, Cancer research.

SYNTHESIS AND ANTILEUKEMIC ACTIVITY OF 5-SUBSTITUTED 2,3-DIHYDRO-6,7-BIS(HYDROXYMETHYL)-1H-PYRROLIZINE DIESTERS

W. Anderson, P. Corey, 1977 .

Mass spectral studies on mesoionic imidazo [1,2‐a] pyrid‐2 and ‐3‐one derivatives

A. Friedman, W. Anderson, 1972 .

A Facile Synthesis of an (E)-4-Methyl-4-Hexenoic Acid Substituted Pyridine Analogue of Mycophenolic Acid

Jeewoo Lee, W. Anderson, 1992 .

Stability of carmethizole hydrochloride (NSC-602668), an experimental cytotoxic agent

V. Stella, R. Killion, W. Anderson, 1991 .

Antileukemic activity of derivatives of 1,2-dimethyl-3,4-bis(hydroxymethyl)-5-phenylpyrrole bis(N-methylcarbamate).

M. J. Halat, W. Anderson, 1979, Journal of medicinal chemistry.

SYNTHESIS OF METHYL 2,3-BIS(HYDROXYMETHYL)-5-PHENYL-7-OXABICYCLO(2.2.1)HEPTA-2,5-DIENE-6-CARBOXYLATE BIS(N-METHYLCARBAMATE) DERIVATIVES AS POTENTIAL ANTITUMOR AGENTS

W. Anderson, B. Mulumba, 1985 .

Allylic esters as potential antitumor agents. Derivatives and analogues of 2,3-bis(hydroxymethyl)-7-oxabicyclo[2.2.1]hept-2-ene.

W. Anderson, R. Dewey, B. Mulumba, 1979, Journal of medicinal chemistry.

1,3-Dipolar cycloaddition reactions with isatin-N-acetic acids. Synthesis of dimethyl 9-oxo-9H-pyrrolo[1,2-a]indole-1,2-dicarboxylates

W. Anderson, P. Corey, 1977 .

Synthesis of 1-Substituted Derivatives of Anhydro(3-chloroacety1-2-hydroxyimidazo [1,2-a]pyridinium Hydroxide)

A. Friedman, W. Anderson, 1971 .

[Bis(aminomethyl)dimethylsilane]platinum(II) dichloride: A potential antitumor agent

J. Plowman, V. Narayanan, R. Haugwitz, 1990 .

SYNTHESIS OF 6,9-BISNORMETHYL-8-METHOXY-12,13-EPOXY-6,8,10-TRICHOTHECATRIENE

George E. Lee, E. LaVoie, W. Anderson, 1977 .

An Improved Synthesis of 5,7-Dimethoxy-4-methylphthalide, A Key Intermediate in the Synthesis of Mycophenolic Acid

G. Makara, K. Klubek, W. Anderson, 1996 .

Tumor inhibitors. XXXIX. Active principles of Acnistus arborescens. Isolation and structural and spectral studies of withaferin A and withacnistin.

A. Burlingame, S. M. Kupchan, H. Schnoes, 1969, Journal of Organic Chemistry.

Steric and electronic factors which effect the thermal cyclization of metasubstituted aryl propargyl ethers. Synthesis of 5- and 7-substituted 3-chromenes

E. LaVoie, P. G. Whitkop, W. Anderson, 1974 .

Synthesis, physical properties, and antitumor activity of tetraplatin and related tetrachloroplatinum(IV) stereoisomers of 1,2-diaminocyclohexane.

V. Narayanan, R. Haugwitz, W. Anderson, 1986, Cancer treatment reports.

AN EFFICIENT SYNTHESIS OF 5,7-DIMETHOXY-4-METHYLPHTHALIDE, A KEY INTERMEDIATE IN THE SYNTHESIS OF MYCOPHENOLIC ACID

G. Makara, W. Anderson, 1995 .

Design, synthesis, and study of 9-substituted ellipticine and 2-methylellipticinium analogues as potential CNS-selective antitumor agents.

A. Gopalsamy, W K Anderson, A Gopalsamy, 1994, Journal of medicinal chemistry.

A One-Pot Method for the Efficient Preparation of Aromatic Nitriles from Aldehydes Using Ammonia, Magnesium Sulfate, and Manganese Dioxide

G. Lai, W. Anderson, N. Bhamare, 2001 .

In vivo and in vitro evaluation of the alkylating agent carmethizole.

D. W. Fry, W. Elliott, W. Leopold, 1991, Cancer research.

Structure, synthesis, and antitumor activity of the hydrolysis product of the antitumor agent carmethizole

M. Jarosinski, P. Van Roey, F. R. Kinder, 1993 .

Vinylogous Carbinolamine Tumor Inhibitors. Part 22. Design, Synthesis, Antineoplastic Activity, and Chemical Properties of Bis(carbamate) Derivatives of 4,5-Bis(hydroxymethyl)imidazole.

D. Bhattacharjee, W. Anderson, D. Houston, 1989 .

Selective Reduction of Carboxylic Acid Esters in the Presence of a Five-Membered Cyclic Sulfone

R. Mach, W. Anderson, 1986 .

Selective Reduction of Carboxylic Acid Esters in the Presence of a Five-Membered Cyclic Sulfone.

R. Mach, W. Anderson, 1987 .

The Synthesis of Amidine Acetals as Intermediates for the Preparation of Naturally Occurring Cyclic Amidine Antibiotics

W. Anderson, N. Raju, 1989 .

Preparation of noncondensed 2-substituted 1-methylimidazoles via ipso substitution reaction on 2-sulfinyl or 2-sulfonyl derivatives of 4,5-disubstituted 1-methylimidazoles

M. Jarosinski, W. Anderson, 1991 .

Preparation of Noncondensed 2‐Substituted 1‐Methylimidazoles via Ipso Substitution Reaction on 2‐Sulfinyl or 2‐Sulfonyl Derivatives of 4,5‐ Disubstituted 1‐Methylimidazoles.

M. Jarosinski, W. Anderson, 1991 .

Synthesis and murine antineoplastic activity of bis[(carbamoyloxy)methyl] derivatives of pyrrolo[2,1-a]isoquinoline.

J. New, W. Anderson, H. Mcpherson, 1984, Journal of Medicinal Chemistry.

SYNTHESIS AND MURINE ANTINEOPLASTIC ACTIVITY OF BIS(CARBAMOYLOXYMETHYL) DERIVATIVES OF PYRROLO(2,1-A)ISOQUINOLINE

J. New, W. Anderson, H. Mcpherson, 1985 .

Synthesis and modeling studies with monocyclic analogues of mycophenolic acid.

T. Boehm, G. Makara, W. Anderson, 1996, Journal of medicinal chemistry.