Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nicholas H. Angello"'
Autor:
Songsong Li, Edward R. Jira, Nicholas H. Angello, Jialing Li, Hao Yu, Jeffrey S. Moore, Ying Diao, Martin D. Burke, Charles M. Schroeder
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-8 (2022)
Development of organic electronic materials relies on understanding structure-function relationships in conjugated polymers but the synthetic workload to make large numbers of new compounds presents a practical barrier to properly survey conjugated o
Externí odkaz:
https://doaj.org/article/f200d886cfc34aad996269b8addf8d6e
Publikováno v:
Molecules, Vol 25, Iss 15, p 3358 (2020)
A new extension for the ‘one pot’ construction of diverse 1-azafluorene derivatives featuring a Diels–Alder/retro-Diels–Alder cycloaddition is reported. Conditions were also determined for oxidation to the derived azafluorenones. The spectrop
Externí odkaz:
https://doaj.org/article/c90b7eef9f914a718e7ec1a2f85b5917
Autor:
Nicholas H. Angello, Vandana Rathore, Wiktor Beker, Agnieszka Wołos, Edward R. Jira, Rafał Roszak, Tony C. Wu, Charles M. Schroeder, Alán Aspuru-Guzik, Bartosz A. Grzybowski, Martin D. Burke
Publikováno v:
Science (New York, N.Y.). 378(6618)
General conditions for organic reactions are important but rare, and efforts to identify them usually consider only narrow regions of chemical space. Discovering more general reaction conditions requires considering vast regions of chemical space der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af305c40468a1531480b1dd61be0ae75
https://pubmed.ncbi.nlm.nih.gov/36302014
https://pubmed.ncbi.nlm.nih.gov/36302014
Autor:
Wiktor Beker, Rafał Roszak, Agnieszka Wołos, Nicholas H. Angello, Vandana Rathore, Martin D. Burke, Bartosz A. Grzybowski
Publikováno v:
Journal of the American Chemical Society. 144(11)
Applications of machine learning (ML) to synthetic chemistry rely on the assumption that large numbers of literature-reported examples should enable construction of accurate and predictive models of chemical reactivity. This paper demonstrates that a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85e3a36c53809c24311f3f7b8ad46eba
https://pubmed.ncbi.nlm.nih.gov/35258973
https://pubmed.ncbi.nlm.nih.gov/35258973
Publikováno v:
Molecules, Vol 25, Iss 3358, p 3358 (2020)
Molecules
Volume 25
Issue 15
Molecules
Volume 25
Issue 15
A new extension for the &lsquo
one pot&rsquo
construction of diverse 1-azafluorene derivatives featuring a Diels&ndash
Alder/retro-Diels&ndash
Alder cycloaddition is reported. Conditions were also determined for oxidation to the d
one pot&rsquo
construction of diverse 1-azafluorene derivatives featuring a Diels&ndash
Alder/retro-Diels&ndash
Alder cycloaddition is reported. Conditions were also determined for oxidation to the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25970eea13f318548348aa91f9b02b26
https://www.mdpi.com/1420-3049/25/15/3358
https://www.mdpi.com/1420-3049/25/15/3358
A new domino reaction sequence for the construction of 2-pyridone structures is reported. The reaction sequence begins with diacetyldiketopiperazine and proceeds via aldol condensation, alkene isomerization, and intramolecular Diels–Alder cycloaddi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4958bf66abb4be27bf18d1cf8d81206f
https://europepmc.org/articles/PMC6220673/
https://europepmc.org/articles/PMC6220673/
