Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ayham H. Abazid"'
Autor:
Khadijah Anwar, Francisco José Aguilar Troyano, Ayham H. Abazid, Oumayma El Yarroudi, Ignacio Funes-Ardoiz, Adrián Gómez-Suárez
Exploration of three-dimensional structural space has become crucial for the development of novel bioactive molecules. In this context, polar spirocycles have emerged as key scaffolds due to their enhanced 3D character and well-defined spatial orient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f8f8645622cd5d424346ce093d69d64
https://doi.org/10.26434/chemrxiv-2023-5jx42
https://doi.org/10.26434/chemrxiv-2023-5jx42
Publikováno v:
Angewandte Chemie. 134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecdd1e643f0ddfe48962bcf68c2c90f4
https://doi.org/10.1002/ange.202216818
https://doi.org/10.1002/ange.202216818
Publikováno v:
Angewandte Chemie International Edition. 61
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4dc711f6d09e19dce5981d83e7394957
https://doi.org/10.1002/anie.202216818
https://doi.org/10.1002/anie.202216818
Publikováno v:
Organic Letters. 23:5076-5080
This study presents an enantioselective oxidative cyclization of N-allyl carboxamides via a chiral triazole-substituted iodoarene catalyst. The method allows the synthesis of highly enantioenriched oxazolines and oxazines, with yields of up to 94% an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d163f82d3208db62ca51b04aafde7935
https://doi.org/10.1021/acs.orglett.1c01607
https://doi.org/10.1021/acs.orglett.1c01607
Publikováno v:
Angewandte Chemie. 134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::195cb6e0b1261e0192331c85c9c38219
https://doi.org/10.1002/ange.202204624
https://doi.org/10.1002/ange.202204624
Publikováno v:
ACS Catalysis. 10:8042-8048
The application of a triazole-substituted chiral iodoarene in a direct enantioselective hydroxylation of alkyl arenes is reported. This method allows the rapid synthesis of chiral benzyl alcohols i...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a7c5cb63473a9b4633281f49742caec
https://doi.org/10.1021/acscatal.0c02321
https://doi.org/10.1021/acscatal.0c02321
Publikováno v:
Angewandte Chemie (International ed. in English). 61(50)
The structure of in situ generated chiral aryl-λ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4be7b85cd1c8a83b806797be272b43e
https://pubmed.ncbi.nlm.nih.gov/35570718
https://pubmed.ncbi.nlm.nih.gov/35570718
Autor:
Ayham H. Abazid, Boris J. Nachtsheim
Publikováno v:
Chemical communications (Cambridge, England). 57(70)
A catalytic highly enantioselective synthesis of spirooxazolines is presented. Starting from readily available 2-naphthol-substituted benzamides and using catalytic amounts of a chiral triazole-substituted iodoarene catalyst, a variety of spirooxazol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60f83e08f7e2200776d5378061ef4324
https://pubmed.ncbi.nlm.nih.gov/34382967
https://pubmed.ncbi.nlm.nih.gov/34382967
Autor:
Ayham H. Abazid, Boris J. Nachtsheim
Publikováno v:
Angewandte Chemie (International Ed. in English)
A widely applicable triazole‐substituted chiral aryl iodide is described as catalyst for enantioselective oxidation reactions. The introduction of a substituent in ortho‐position to the iodide is key for its high reactivity and selectivity. Besid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f3e5594bf79f737bd534d0b15341d6e
https://doi.org/10.1002/ange.201912023
https://doi.org/10.1002/ange.201912023
Publikováno v:
Organic letters. 23(13)
This study presents an enantioselective oxidative cyclization of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc534139520eef9c535da868b4466c96
https://pubmed.ncbi.nlm.nih.gov/34138574
https://pubmed.ncbi.nlm.nih.gov/34138574