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pro vyhledávání: '"Vidya D. Avasare"'
Phosphine‐Free Ruthenium Complex for Hydrogenation of Carbonyl Compounds: Synthesis and Applications
Autor:
Suraj B. Maldode, Suribabu Sattineni, Vidya D. Avasare, A. M. Sathiyanarayanan, K. Shashikumar, Sachinkumar Sajjanar, Sambasivam Ganesh, Amol V. Gadakh, Shivaprasad N. Hegde
Publikováno v:
ChemistrySelect. 6:8411-8415
Autor:
Vidya D. Avasare
Publikováno v:
Inorganic chemistry. 61(4)
The development of sustainable catalysts to get methanol from CO2 under milder conditions and without any additives is still considered an arduous task. In many instances, transition-metal-catalyzed carbon dioxide to formic acid formation is more fac
Publikováno v:
Tetrahedron. 64:8943-8946
Photochemical reaction between the enynes, (Z)-1-methoxybut-1-ene-3-yne, 1 or isopropenyl acetylene, 2 with CO in presence of Fe(CO)5 yields the 2,6- and 2,5-divinyl-substituted 1,4-benzoquinones: 2,6-bis{(Z)-2-methoxyvinyl}-1,4-benzoquinone (3, 42%)
Publikováno v:
IndraStra Global.
Photochemical reaction of methanol solution containing 1,4-diferrocenyl- or 1,4-diphenyl-1,3-butadiynes and iron pentacarbonyl into which CO was constantly bubbled, yielded diiron hexacarbonyl complexes of cumulene ligand systems, [η1: η3-{RCHC2CR(
Publikováno v:
ChemInform. 39
Publisher Summary This chapter focuses on mixed-metal acetylide complexes that are prepared from metal–acetylide precursor complexes. Particular emphasis is given to the aspects of variation of acetylide bonding on mixed-metal polynuclear framework
Publisher Summary This chapter focuses on mixed-metal acetylide complexes that are prepared from metal–acetylide precursor complexes. Particular emphasis is given to the aspects of variation of acetylide bonding on mixed-metal polynuclear framework
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1573b087a3dba0cd8349dd4c305717b1
https://doi.org/10.1016/s0065-3055(07)55004-5
https://doi.org/10.1016/s0065-3055(07)55004-5
Publikováno v:
IndraStra Global.
Molybdenum dithiopropiolato complexes, [(η5-C5R4R′)Mo(CO)2(η2-S2CC≡CPh)] (R=H, R=Me 1a, R=R′=H 1b; R=R′=Me 1c) react with trimethylamine-N-oxide (TMNO · 2H2O) under mild thermolysis to form 5-phenyl-1,2-dithiole-3-thione (2). The reaction