Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Peter Hammar"'
Autor:
Peter Hammar
Publikováno v:
SMPTE Motion Imaging Journal. 131:59-59
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::420ee01c74926f8ed1e4770c8c295195
https://doi.org/10.5594/jmi.2022.3164415
https://doi.org/10.5594/jmi.2022.3164415
Publikováno v:
2017 Workshop on Research, Education and Development of Unmanned Aerial Systems (RED-UAS).
We address the issue of autonomously planning a flight path for a remotely controlled surveillance aircraft when control is lost due to jamming. An optimization problem arises where we want the aircraft to continue surveying in the jammed area so tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3f7e63d43a097b1e578ae529764f446
https://doi.org/10.1109/red-uas.2017.8101647
https://doi.org/10.1109/red-uas.2017.8101647
Publikováno v:
SMC
This paper provides an example of using genetic programming for engendering computational creativity in computer generated forces, i.e. simulated entities used to represent own, opponent and neutral forces in military training or decision support app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b8fc57cad8f334ad805986a4c52e110
https://doi.org/10.1109/smc.2016.7844707
https://doi.org/10.1109/smc.2016.7844707
Publikováno v:
Advances in Intelligent Systems and Computing ISBN: 9783319274775
KICSS
KICSS
We describe a decision support system for hypothesis assessment in which exploration is supported by computational creativity. A software tool for morphological hypothesis analysis and evidence handling is extended with a creative assistant that on d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f50f4cc063051cc9e43959c6b808a15
https://doi.org/10.1007/978-3-319-27478-2_6
https://doi.org/10.1007/978-3-319-27478-2_6
Autor:
Peter Hammar
Publikováno v:
SMPTE Motion Imaging Journal. 127:108-108
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::088e77a8ebaf9cc90c6125bca86c9776
https://doi.org/10.5594/jmi.2018.2856639
https://doi.org/10.5594/jmi.2018.2856639
Autor:
Peter Hammar, Cynthia Ghobril, Sanjeevarao Kodepelly, Fahmi Himo, Bernard Spiess, Alain Wagner, Rachid Baati
Publikováno v:
ChemCatChem. 2:1573-1581
Structure-reactivity studies are performed to explore the reaction mechanism of the guanidine-catalyzed intramolecular aldol reaction of ketoaldehydes. A large number of guanidine and guanidine-lik ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08a201d4fb24e4214ae327d08df4ee1b
https://doi.org/10.1002/cctc.201000227
https://doi.org/10.1002/cctc.201000227
Publikováno v:
Advanced Synthesis & Catalysis. 351:525-529
The reason for enantioselectivity in thereductive amination of α-branched aldehydes wasinvestigated. The relative energies of all the diastereomeric transition states for hydride transfer of a suit ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0454050e873ec58016b4f96315b3291b
https://doi.org/10.1002/adsc.200800613
https://doi.org/10.1002/adsc.200800613
Autor:
Peter Hammar
Publikováno v:
SMPTE Motion Imaging Journal. 118:16-19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f65e932c4294902442490f91962aca1a
https://doi.org/10.5594/j14986
https://doi.org/10.5594/j14986
Publikováno v:
Chemistry - A European Journal. 14:8562-8571
The phosphoric acid catalyzed reaction of 1,4-dihydropyridines with N-arylimines has been investigated by using density functional theory. We first considered the reaction of acetophenone PMP-imine (PMP=p-methoxyphenyl) with the dimethyl Hantzsch est
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d0138122e535be690967ef19c3c9105
https://doi.org/10.1002/chem.200800890
https://doi.org/10.1002/chem.200800890
Publikováno v:
Tetrahedron: Asymmetry. 19:1617-1621
The origins of the stereoselection of the dipeptide-catalyzed intermolecular aldol reaction are explored by means of hybrid density functional theory. Transition states were located for the (S)-ala-(S)-ala-catalyzed aldol reaction with cyclohexanone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f350043fd8a473ac814e5d4655245114
https://doi.org/10.1016/j.tetasy.2008.06.014
https://doi.org/10.1016/j.tetasy.2008.06.014