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Controlled formation of dipyranoside derivatives through C6 and O4: pyranosidic homologation. VIIMOLINO, B. F; FRASER-REID, B.Canadian journal of chemistry (Print). 1987, Vol 65, Num 12, pp 2834-2842, issn 0008-4042Article

Pyranosidic homologation. I: Extending the carbohydrate template via C6 and C4MOLINO, B. F; MAGDZINSKI, L; FRASER-REID, B et al.Tetrahedron letters. 1983, Vol 24, Num 52, pp 5819-5822, issn 0040-4039Article

Constrained β-alanine based GpIIb/IIIa antagonistsKLEIN, S. I; CZEKAJ, M; MOLINO, B. F et al.Bioorganic & medicinal chemistry letters (Print). 1997, Vol 7, Num 13, pp 1773-1778, issn 0960-894XArticle

Conformationally flexible platelet aggregation inhibitors based on the tetrapeptide Arg-Gly-Asp-ArgKLEIN, S. I; CZEKAJ, M; MOLINO, B. F et al.European journal of medicinal chemistry. 1997, Vol 32, Num 10, pp 833-839, issn 0223-5234Article

Dipyranoside precursors for ansamycins. Pyranosidic homologation. 5FRASER-REID, B; MAGDZINSKI, L; MOLINO, B. F et al.Journal of organic chemistry. 1987, Vol 52, Num 20, pp 4495-4504, issn 0022-3263Article

Tripyranoside precursors for ansamycins. Pyranosidic homologation. VIFRASER-REID, B; MOLINO, B. F; MAGDZINSKI, L et al.Journal of organic chemistry. 1987, Vol 52, Num 20, pp 4505-4511, issn 0022-3263Article

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