A 1% crosslinked divinylbenzene-styrene copolymer was used in the preparation of the unsymmetrical 2-(6'-hydroxyhexoxy)-9,16,23-triisopropoxyphthalocyanine, soluble in common organic solvents.
The synthesis of oligodeoxyprimidines on a polymer support
β Scribed by M.D. Matteucci; M.H. Caruthers
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- French
- Weight
- 274 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A polymer supported method for synthesizing deoxypolynucleotides is described . Two nonanucleotides were synthesized . Yields exceeding 90% were obtained for each condensation . The time per nucleotide addition was four hours .
Attempts to develop a successful methodology for synthesizing sequence defined oligonucleotides have been numerous l ' 2 . However despite these achievements the stepwise synthesis of oligonucleotides still remains a difficult and time consuming task . We are developing procedures which should solve this problem . This communication outlines our initial results on adapting the phosphite coupling procedure 3 to polymer supported polynucleotide synthesis .
Classically a major problem with polymer supported synthetic strategies has been the polymer support . Various polymers have been shown to be inadequate for reasons such as slow diffusion rates into the support, excessive swelling of various macroporous, low crosslinked polymers and
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A highly hydrophobic N-methoxytrityloxyethylaniline(MTEA) was introduced for the protection of 5 '-phosphate of thymidine. A MTEA group at the phosphodiester level is cleaved by aqueous acetic acid. By using MTEA group, 5'-phosphorylated hexadecadeoxyribonucleotide was rapidly synthesized on a polym
A number of feasible approaches for the solid-phase synthesis of oligosaccharides, using protecting group chemistry, have been published in recent years [l-4]. Nevertheless, a widespread use of these approaches suffers from the fact that there is no chemical glycosylation method that is generally a