C. H. M. Verdegaal

Synthesis of oligonucleotides with sequences identical with or analogous to the 3′ - end of I6S ribosomal RNA of Escherichia coli: preparation of A-C-C-U-C-C via the modified phosphotriester method¹

Jacques H. van Boom, Peter Burgers, G. van der Marel et al. · Nucleic Acids Research · 1977 · 70 citations · Full text

Biosynthesis, Bioorganic Chemistry, Engineering +15

Acid-catalysed isomerization of the tetraisopropyldisiloxane-1,3-diyl group. Simultaneous protection of two secondary alcoholic functions.

C. H. M. Verdegaal, P. L. Jansse, J.F.M. de Rooij et al. · Tetrahedron Letters · 1980 · 61 citations

Acid-catalysed Isomerization, Secondary Alcoholic Functions, Engineering +9

Synthesis of oligonucleotides with sequences identical with or analogous to the 3'-end of 16s ribosomal rna of escherichia coli: preparation op U-C-C-U-U-A and A-C-C-U-C-C-U-U-A via the modified phosphotriester method

Jacques H. van Boom, Peter Burgers, C. H. M. Verdegaal et al. · Tetrahedron · 1978 · 20 citations

Biosynthesis, Engineering, Ribosomal Rna +13

4,4‐(Ethylenedithio)pentanoyl: A masked levulinoyl protective group in the synthesis of oligosaccharides

H. J. Koeners, C. H. M. Verdegaal, J. H. VAN BOOM · Recueil des Travaux Chimiques des Pays-Bas · 1981 · 13 citations

Biosynthesis, Bioorganic Chemistry, Biomanufacturing +15

A convenient synthesis of 2′‐<i>O</i>‐acetal‐<i>N</i>²‐acyl derivatives of riboguanosine

C. H. M. Verdegaal, P. L. Jansse, J.F.M. de Rooij et al. · Recueil des Travaux Chimiques des Pays-Bas · 1981 · 10 citations

Derivatives, Engineering, Biochemistry +12