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Synthesis and reactions of dipyrromethane-2,10-dicarboxylates
✍ Scribed by Antonio Garrido Montalban; Antonio J. Herrera; Jes Johannsen; Josephine Beck; Thomas Godet; Marianna Vrettou; Andrew J.P. White; David J. Williams
- Book ID
- 104250515
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 78 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Dipyrromethane-2,10-dicarboxylates have been prepared. While oxidation and subsequent reaction of 5b with BF 3 •OEt 2 yields the corresponding complex 10, ring-closing metathesis of 5d using (NHC)(PCy 3 )(Cl) 2 Ru CHPh 7 results in the novel hybrid macrocycle 8. The structure of 10 has been unequivocally established by an X-ray crystallographic study.
📜 SIMILAR VOLUMES
## Abstract Dimethyl 3‐[(4‐nitro)phenyl]aziridine‐2,2‐dicarboxylate (3a) represents a new, photochromic aziridine. 3a and related aziridines undergo cycloadditions with dipolarophiles to form five‐membered heterocycles and react with nucleophiles with cleavage of the C^2^C^3^ bond.
A 3 and trans-A 2 B tris-aryl corroles 1a-c have been synthesized in up to 12% yield by BF 3 •Et 2 O-catalyzed condensation of dipyrromethane-dicarbinol and 2,2%-bipyrrole (1:1 ratio) in acetonitrile at room temperature for 24 h.