B. Clare

发表

Carbonic anhydrase activators. 3: structure-activity correlations for a series of isozyme II activators.

C. Supuran, B. Clare, C T Supuran, 1994, Journal of pharmaceutical sciences.

QSAR of Aromatic Substances: Protein Tyrosine Kinase Inhibitory Activity of Flavonoid Analogues

O. Deeb, B. Clare, Brian W. Clare, 2007, Chemical biology & drug design.

Carbonic anhydrase inhibitors. Part 61. Quantum chemical QSAR of a group of benzenedisulfonamides

Claudiu T. Supuran, Brian W. Clare, C. Supuran, 1999 .

Carbonic anhydrase inhibitors - Part 57 : Quantum chemical QSAR of a group of 1,3,4-thiadiazole- and 1,3,4-thiadiazoline disulfonamides with carbonic anhydrase inhibitory properties

C. Supuran, B. Clare, B. W. Clare, 1999 .

The enhanced stability of endo isomers of C60F60

B. Clare, B. W. Clare, D. Kepert, 1996 .

The structures of atom clusters. Nido, arachno, hypho and planar aromatic molecules

B. Clare, D. Kepert, 1984 .

Electron-rich boranes and related molecules

B. Clare, D. Kepert, 1987 .

Protease inhibitors: synthesis and QSAR study of novel classes of nonbasic thrombin inhibitors incorporating sulfonylguanidine and O-methylsulfonylisourea moieties at P1.

C. Supuran, A. Scozzafava, B. Clare, 2000, Journal of medicinal chemistry.

Evidence for the S(N)2' mechanism in hydrolysis of C60F48: origin of the stability of trannulenes.

R. Taylor, B. Clare, B. W. Clare, 2003, Organic & biomolecular chemistry.

In the first proven SN2' fullerene reaction, both C3 and C1 C60F36 hydrolyse to C1 isomers of C60F35OH that eliminate HF to give epoxides C60F34O; C60F36O oxides are shown to be ethers, and a fourth isomer of C60F36 exists.

R. Taylor, B. Clare, B. W. Clare, 2003, Organic & biomolecular chemistry.