Zobrazeno 1 - 10
of 32
pro vyhledávání: '"A. I. Arkhypchuk"'
Publikováno v:
ChemPlusChem.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dec7b93cc5492e0a851818b91e721bed
https://doi.org/10.1002/cplu.202300067
https://doi.org/10.1002/cplu.202300067
Autor:
Nicolas D'Imperio, Valentina Pelliccioli, Sara Grecchi, Alberto Bossi, Francesca Vasile, Silvia Cauteruccio, Anna I. Arkhypchuk, Arvind Kumar Gupta, Andreas Orthaber, Sascha Ott, Emanuela Licandro
Publikováno v:
European Journal of Organic Chemistry. 26
The first examples of a pi-conjugated benzo[b]phosphole P-oxide in which two phosphole P-oxide units are connected by a carbon-carbon double bond are described. The molecules are synthesized as E isomers with respect to the carbon-carbon double bond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21359dbd6617562bb6515ae4ccb61958
https://doi.org/10.1002/ejoc.202201209
https://doi.org/10.1002/ejoc.202201209
Publikováno v:
Chemical science. 13(41)
Procedures for the reductive coupling of carbonyl compounds to alkenes in the literature rely either on a radical coupling strategy, as in the McMurry coupling, or ionic pathways, sometimes catalysed by transition metals, as in more contemporary cont
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba2f9ed6d051960d55be24a9e281f4d6
https://pubmed.ncbi.nlm.nih.gov/36349090
https://pubmed.ncbi.nlm.nih.gov/36349090
Current methodologies for the direct reductive coupling of two aldehydes to alkenes afford almost exclusively the thermodynamically favoured E-isomer. Recent efforts to find phosphorus-based reagents as replacements for the low-valent Ti species in M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e19a70a7fba8de3569cbe1ecd662d5f
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-490320
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-490320
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 23:589-598
Unlike N-confused porphyrins which are well-known and extensively studied tetrapyrroles, N-confused hydroporphyrins are almost unknown, largely because so far they have resisted attempts at rational synthesis. Here, we report our efforts towards the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3aac2c360b12ed67072d6f62a9bf7c1
https://doi.org/10.1142/s1088424619500524
https://doi.org/10.1142/s1088424619500524
Publikováno v:
European Journal of Inorganic Chemistry. 2019:1562-1566
Triphenylphosphaalkenes 1a-c were prepared in good to excellent yields in a modified phospha-Peterson reaction between PhP(Li)TMS and benzophenones with different para-substituents at the C-phenyl ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::884bb6b22d4ac5af6ee26ce2e41f2eaf
https://doi.org/10.1002/ejic.201801322
https://doi.org/10.1002/ejic.201801322
Publikováno v:
European Journal of Organic Chemistry. 2018:7051-7056
A simple protocol for the controlled preparation of mono- and diprotonated hydroporphyrins (chlorins) is presented. The chlorins carried 10-aryl groups with electron-neutral (phenyl), electron-dona ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0a3072a1472b4a1950aaa0559e3034b
https://doi.org/10.1002/ejoc.201801472
https://doi.org/10.1002/ejoc.201801472
Autor:
Martin Obermeier, Anna I. Arkhypchuk
Publikováno v:
The Journal of organic chemistry. 84(6)
The reactivity of phosphanyl phosphonates toward diacetylenic ketones was studied. Reactions resulted in the selective formation of phospholones via phosphaalkene intermediates. Phospholones were obtained in yields of 37-96% depending on the substitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::305c2cbbf01f42f1de6d2cdb51d61f8d
https://pubmed.ncbi.nlm.nih.gov/30788966
https://pubmed.ncbi.nlm.nih.gov/30788966
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
The de novo syntheses of chemically stable chlorins with five‐membered heterocyclic (furane, thiophene, formylfurane and formylthiophene) substituents in selected meso‐ and β‐positions are reported. Heterocycle incorporation in the 3‐ and 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a7199502d5368f54722a7c23009efc3
https://doi.org/10.1002/chem.201604655
https://doi.org/10.1002/chem.201604655