Application of combinatorial techniques in the synthesis of unsymmetrically substituted 5,15-diphenylporphyrins
β Scribed by Kerry J Elgie; Martin Scobie; Ross W Boyle
- Book ID
- 104210115
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 206 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Combinatorial techniques, both solid and solution phase, have been applied to the synthesis of unsymmetrically substituted 5,15-diphenylporphyrins. 5-(4-Hydroxyphenyl)-15-pentafluorophenylporphyrin can be loaded onto solid supports and substituted on the pentafluorophenyl ring with thiols. Diversity is then expanded by cleavage and solution phase substitution of the second phenyl ring using a solid supported base.
π SIMILAR VOLUMES
The synthesis of Boc-or Fmoc-monoprotected propylenediamine derivatives is reported starting from N-protected a-amino acids. The introduction of these building blocks on solid support via the formation of a urea moiety leads to a new pseudopeptide family (Ca-CHe-CH~-Na(R)-CO-NH-Ca). Two carbonylati