M. Greenlee

发表

Ibrexafungerp: an orally active β-1,3-glucan synthesis inhibitor.

P. Liberator, M. Motyl, M. Peel, 2020, Bioorganic & medicinal chemistry letters.

MK-5204: An orally active β-1,3-glucan synthesis inhibitor.

P. Liberator, M. Motyl, M. Peel, 2020, Bioorganic & medicinal chemistry letters.

Discovery of betamethasone 17alpha-carbamates as dissociated glucocorticoid receptor modulators in the rat.

Amjad Ali, M. Forrest, G. Harris, 2008, Bioorganic & medicinal chemistry.

Novel orally active inhibitors of β-1,3-glucan synthesis derived from enfumafungin.

P. Liberator, M. Motyl, M. Peel, 2015, Bioorganic & medicinal chemistry letters.

Inhibition of IMP-1 metallo-beta-lactamase and sensitization of IMP-1-producing bacteria by thioester derivatives.

B. Leiting, D. Pompliano, J. Balkovec, 1999, FEMS microbiology letters.

Dicationic 2-fluorenonylcarbapenems: potent anti-MRS agents with improved solubility and pharmacokinetic properties.

M. Greenlee, M. Hammond, J. Huber, 1999, Bioorganic & medicinal chemistry letters.

Succinic Acids as Potent Inhibitors of Plasmid-borne IMP-1 Metallo-β-lactamase*

N. Sharma, P. Fitzgerald, S. Olson, 2001, The Journal of Biological Chemistry.

Triazolo-tetrahydrofluorenones as selective estrogen receptor beta agonists.

S. Nilsson, A. Thorsell, L. Colwell, 2006, Bioorganic & medicinal chemistry letters.

Selective glucocorticoid receptor nonsteroidal ligands completely antagonize the dexamethasone mediated induction of enzymes involved in gluconeogenesis and glutamine metabolism

Amjad Ali, W. Geissler, G. Harris, 2004, The Journal of Steroid Biochemistry and Molecular Biology.

2-Naphthylcarbapenems: broad spectrum antibiotics with enhanced potency against MRSA.

C. Jaworsky, M. Greenlee, F. Dininno, 1999, Bioorganic & medicinal chemistry letters.

A highly efficient method for the preparation of 2-aryl substituted carbapenems exploiting a Pd(0) mediated cross-coupling reaction.

T. Rano, M. Greenlee, F. Dininno, 1990 .

Estrogen receptor beta-subtype selective tetrahydrofluorenones: use of a fused pyrazole as a phenol bioisostere.

S. Nilsson, A. Thorsell, L. Colwell, 2006, Bioorganic & medicinal chemistry letters.

Synthetic Study toward Total Synthesis of (±)-Germine: Synthesis of (±)-4-Methylenegermine.

A. Clark, P. Parsons, M. Kitamura, 2017, Organic letters.

The synthesis and anti-MRSA activity of amidinium-substituted 2-dibenzofuranylcarbapenems.

M. Greenlee, J. Huber, J. Sundelof, 1999, Bioorganic & medicinal chemistry letters.

Synthesis and SAR of thioester and thiol inhibitors of IMP-1 Metallo-β-Lactamase

David L. Pompliano, James M. Balkovec, D. Pompliano, 1999 .

Synthesis and biological evaluation of antifungal derivatives of enfumafungin as orally bioavailable inhibitors of β-1,3-glucan synthase.

P. Liberator, G. J. Pacofsky, M. Peel, 2012, Bioorganic & medicinal chemistry letters.

X-RAY AND THEORETICAL ANALYSIS OF THE RELATIONSHIP BETWEEN SUBSTITUENT STERIC EFFECTS AND THE STRUCTURE OF BICYCLO(1.1.0)BUTANE. THE UNEXPECTED FLEXIBILITY OF THE BICYCLO(1.1.0)BUTANE SKELETON

P. G. Gassman, D. Dixon, S. Richtsmeier, 1983 .

X-ray and theoretical analysis of the relationship between substituents steric effects and the structure of bicyclo[1.1.0]butane: the unexpected flexibility of the bicyclo[1.1.0]butane skeleton

P. G. Gassman, D. Dixon, S. Richtsmeier, 1983 .

Use of fluoroalkyl as a latent group for internal alkylation: application to the synthesis of bridged tetrahydrofluorenones.

D. Parker, D. Meng, M. Greenlee, 2008, Organic letters.

TOTAL SYNTHESIS OF (.+-.)-TRIHYDROXYDECIPIADIENE

M. Greenlee, 1981 .