Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Masao WADA"'
Publikováno v:
Computers and Geotechnics. 160:105548
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d7a631735ce884de4ce162f5d65e123
https://doi.org/10.1016/j.compgeo.2023.105548
https://doi.org/10.1016/j.compgeo.2023.105548
Publikováno v:
Japanese Geotechnical Journal. 15:67-79
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::138ceb0931f4a5c5330aebdafcc6dce5
https://doi.org/10.3208/jgs.15.67
https://doi.org/10.3208/jgs.15.67
Autor:
Masao Wada
Publikováno v:
Marine Engineering. 52:744-746
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7da009b68c13f4810b6f66885691c6c8
https://doi.org/10.5988/jime.52.744
https://doi.org/10.5988/jime.52.744
Publikováno v:
Tetrahedron. 69:4325-4330
Hydrazones obtained from α-diazo esters were converted to pyrroles when heated with thionyl chloride in alcohol. Among hydrazones, those substituted with a benzene ring on the β-carbon to the ester are likely to give pyrroles in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d3d3f911d7eac2182b39a7d6caa6029
https://doi.org/10.1016/j.tet.2013.03.037
https://doi.org/10.1016/j.tet.2013.03.037
Publikováno v:
Tetrahedron Letters. 50:4762-4765
We have developed a novel method for the synthesis of 3,4-diarylpyrrole-2,5-dicarboxylates via α-diazo esters, which are easily obtained from phenylalanine derivatives. Utilizing this method, intermediates of bioactive compounds having the structure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e500006995f11b02f86e3770223be310
https://doi.org/10.1016/j.tetlet.2009.06.012
https://doi.org/10.1016/j.tetlet.2009.06.012
Publikováno v:
Tetrahedron. 65:461-468
Aryl hydrazones, the precursor of Fischer indole synthesis, were easily obtained by nucleophilic addition of aryllithium reagents to diazo esters. The aryl hydrazones were converted into indoles in good yields by heating with thionyl chloride in alco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9fd7ebeddfcecb2d9747b1c379918cc
https://doi.org/10.1016/j.tet.2008.11.028
https://doi.org/10.1016/j.tet.2008.11.028
Publikováno v:
PROCEEDINGS OF CIVIL ENGINEERING IN THE OCEAN. 24:885-890
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40387be3166e5b5a6bcbffc91f71f626
https://doi.org/10.2208/prooe.24.885
https://doi.org/10.2208/prooe.24.885
Autor:
Masaaki Sakuraba, Masao Wada, Junichi Nakahira, Taro Arikawa, Tsutomu Sakakiyama, Atsuhito Inoue
Publikováno v:
PROCEEDINGS OF CIVIL ENGINEERING IN THE OCEAN. 24:867-872
CADMAS-SURF is a useful numerical model to design maritime structure. Applicability of CADMAS-SURF for predictions of breaking waves or irregular waves has been studied. However, there are not many studies about the wave run-up problems. It is necess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c68b325ececeb68cc17ce54b48624aa5
https://doi.org/10.2208/prooe.24.867
https://doi.org/10.2208/prooe.24.867
Publikováno v:
Tetrahedron Letters. 47:743-746
A novel method for synthesizing arylhydrazones, the precursor for Fischer indole synthesis, using aryllithium reagents and α-diazo esters that are easily obtained from α-amino acid esters, is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1edb8214726dd801dfb8364c4b915e1b
https://doi.org/10.1016/j.tetlet.2005.11.126
https://doi.org/10.1016/j.tetlet.2005.11.126
Publikováno v:
Journal of Electron Microscopy. 52:153-159
A variable-pressure scanning electron microscopy (VP-SEM) with a cooling stage permits long hours of observation of water-containing specimens in their natural or close to natural state, without the conventional specimen preparations of fixation, deh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ff95449cb00521db411ceb980014ab7
https://doi.org/10.1093/jmicro/52.2.153
https://doi.org/10.1093/jmicro/52.2.153