Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Bushi Chen"'
Publikováno v:
IEEE Robotics and Automation Letters. 8:1571-1578
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c9838fdec272563827de42d80cf41b1
https://doi.org/10.1109/lra.2023.3240372
https://doi.org/10.1109/lra.2023.3240372
Publikováno v:
ChemInform. 23
Syntheses of Rh(II) carboxylate salts of terminally funcfionalized polyethylene carboxylic acids arc described. These polymer-bound transition metals are homogeneous catalysts for cyclopropanation of alkenes at 100°C and have activities and selectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f3a84d02c9a0c4fbe1284c517750277
https://doi.org/10.1002/chin.199213157
https://doi.org/10.1002/chin.199213157
Publikováno v:
Scopus-Elsevier
The use of soluble triphenylphosphine ligands to activate Pd(0) catalysts for allylic substitution of allyl esters or ethers by amines and stabilized carbanion nucleophiles and carboalkoxylation of aryl iodides and decar☐ylation of allylic β-keto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08763ef81723dacf569182fd3e7a7e0b
https://doi.org/10.1016/0304-5102(92)80258-i
https://doi.org/10.1016/0304-5102(92)80258-i
Publikováno v:
The Journal of Organic Chemistry. 48:4179-4186
Reaction de derives organometalliques de metal alcalin reactifs du polystyrene reticule avec des solutions de dichloro (cyclooctadiene-1,5) palladium (II) pour former des catalyseurs palladium/polystyrene. Caracterisation par ESCA et microscopie elec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9b00f90a2ae2c5faf894c111847b6b9
https://doi.org/10.1021/jo00171a005
https://doi.org/10.1021/jo00171a005
Publikováno v:
Journal of Macromolecular Science: Part A - Chemistry. 24:289-300
Palladium complex-catalyzed double carbonylation is a recently discovered reaction in organotransition metal chemistry. In this paper, some polymer-bound palladium complexes-polystyrylphosphine-palladium(0) complexes, poly-2-vinylpyridine-palladium(I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aefc1d9c5c4238166d8c0a29d4d36d21
https://doi.org/10.1080/00222338708074446
https://doi.org/10.1080/00222338708074446
Publikováno v:
The Journal of Organic Chemistry. 48:5366-5368
Methode tres simple et commode pour la formation de derives metal alcalin de polystyrenes reticules par le divinylbenzene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6324e28c9ae1fe08b11bb67210bb5482
https://doi.org/10.1021/jo00174a044
https://doi.org/10.1021/jo00174a044
Autor:
Bushi Chen, David E. Bergbreiter
Publikováno v:
Chemischer Informationsdienst. 15
Allylic substitution of the acetoxy group of allylic acetates by various nucleophiles is catalysed by heterogeneous palladium catalysts in the presence of triphenylphosphine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6270c49d9851809ed516591e6da1098f
https://doi.org/10.1002/chin.198410090
https://doi.org/10.1002/chin.198410090
Publikováno v:
Scopus-Elsevier
Syntheses of Rh(II) carboxylate salts of terminally funcfionalized polyethylene carboxylic acids arc described. These polymer-bound transition metals are homogeneous catalysts for cyclopropanation of alkenes at 100°C and have activities and selectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aff3e77197b2b1bcabf72ede2615cb4c
http://www.scopus.com/inward/record.url?eid=2-s2.0-0025877971&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0025877971&partnerID=MN8TOARS
Autor:
Bushi Chen, David E. Bergbreiter
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :1238
Allylic substitution of the acetoxy group of allylic acetates by various nucleophiles is catalysed by heterogeneous palladium catalysts in the presence of triphenylphosphine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08eae8a69042eba76bdc8b4b13229500
https://doi.org/10.1039/c39830001238
https://doi.org/10.1039/c39830001238
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