C. Brosa

发表

BRASSINOSTEROIDS : A NEW WAY TO DEFINE THE STRUCTURAL REQUIREMENTS

I. Zamora, C. Brosa, Joan Miquel Capdevila, 1996 .

β-Phenyl quenching of 9-phenylphenalenones: a novel photocyclisation reaction with biological implications.

S. Nonell, C. Flors, G. Bucher, 2014, Physical chemistry chemical physics : PCCP.

Synthesis of 4-methylumbelliferyl-β-d-glucan oligosaccharides as specific chromophoric substrates of (1 → 3),(1 → 4)-β-d-glucan 4-glucanohydrolases

A. Planas, J. Viladot, C. Brosa, 1995 .

Biological effects of brassinosteroids.

C. Brosa, 1999, Critical reviews in biochemistry and molecular biology.

New synthetic brassinosteroids: a 5α-hydroxy-6-ketone analog with strong plant growth promoting activity

J. Ferrer, C. Brosa, E. Terricabras, 1998 .

Synthesis of new brassinosteroids with epoxy functions: The effect on the regioselectivity of the Baeyer-Villiger reaction

X. Miró, C. Brosa, 1997 .

The cathodic reduction of activated olefins. Experimental conditions allowing the specific hydrogenation of the enone derived from ergosterol

J. Simonet, C. Brosa, C. Rodríguez-Santamarta, 2001 .

A brassinosteroid derivative useful to provide more information about the importance of the C2 group in the brassinosteroid-receptor interaction

M. Piqué, C. Brosa, M. Amoros, 2002 .

Brassinosteroids: A New Way to Define the Structural Requirements.

I. Zamora, C. Brosa, Joan Miquel Capdevila, 1996 .

Synthesis and bioactivity of C-29 brassinosteroid analogues with different functional groups at C-6.

J. Ramirez, L. Galagovsky, C. Brosa, 2005, Phytochemistry.

Use of dihydroquinidine 9-O-(9'-phenanthryl) ether in osmium-catalyzed asymmetric dihydroxylation in the synthesis of brassinosteroids

R. Peracaula, M. Ventura, C. Brosa, 1992 .

Synthesis and molecular modeling: Related approaches to progress in brassinosteroid research

I. Zamora, R. Peracaula, C. Brosa, 1997, Lipids.

The synthesis of androstane brassinosteroid analogues with α-azido acid ester groups in position 17β

L. Kohout, Barbora Slavı́ková, C. Brosa, 2010, Steroids.

New brassinosteroid analogs having nitrogenated functionalities at C3 to provide more information about the brassinosteroid–receptor interaction

C. Brosa, Xaviera Hernández, M. Amoros, 2004 .

Stereochemical course and structure of the products of the enzymic action of endo-1,3-1,4-beta-D-glucan 4-glucanohydrolase from Bacillus licheniformis.

A. Planas, M. Bernabé, C. Brosa, 1993, The Biochemical journal.

Photo‐oxygenation of Styrenic Estrogens: Structural Analysis of 8,9‐Didehydro‐, 6,7‐Didehydro‐, and 9,11‐Didehydroestrone Derivatives and Their Reactivity towards Singlet Oxygen

J. Rius, A. Planas, J. F. Piniella, 1991 .

A new efficient procedure for the reduction of Δ7 ergostane derivatives

C. Brosa, C. Rodríguez-Santamarta, 1999 .

New synthetic strategy for the synthesis of 24-epibrassinolide

X. Comas, C. Brosa, C. Fernandez, 1996, Steroids.

Short step synthesis of (22E, 24R)-5α-ergosta-2,22-dien-6-one, a key intermediate for the preparation of 24-epibrassinolide

J. Ferrer, O. Saavedra, C. Brosa, 1990 .

The Effect of Electrostatic Properties and Abibility to Form Hydrogen-Bonds on the Activity of Brassinosteroid Side-Chain Analogs

L. Kohout, I. Zamora, C. Brosa, 1998 .