Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Patrik Krumlinde"'
Publikováno v:
Propellants, Explosives, Pyrotechnics. 42:78-83
Propellants containing nitrocellulose (NC) continuously decompose. The decomposition products released in the process increase the rate of the decomposition and a self-accelerating behavior is obtained. To prevent the autocatalysis, stabilizers are a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c9bdd5fecd9d72a4f3b20a50fc542d7
https://doi.org/10.1002/prep.201600122
https://doi.org/10.1002/prep.201600122
Publikováno v:
European Journal of Organic Chemistry
Ruthenium-catalysed epimerisation of secondary carbohydrate alcohols was used to determine the thermodynamic equilibrium between non-anomeric epimers of partially protected glucose, mannose and allose derivatives. A cyclopentadienylruthenium catalyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9550f19c6b29e12c0a79221af4ec232b
https://doi.org/10.1002/ejoc.201100504
https://doi.org/10.1002/ejoc.201100504
Publikováno v:
European Journal of Organic Chemistry. 2011:4409-4414
Wilkinson’s catalyst [RhCl(PPh3)3] was heterogenized on common silica by the use of a grafting/anchoring technique. The immobilized catalyst showed high activity and selectivity in transfer hydroge ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c8cb433b786b16fed6cddf3439a7809
https://doi.org/10.1002/ejoc.201100339
https://doi.org/10.1002/ejoc.201100339
Publikováno v:
The Journal of Organic Chemistry
Chemoenzymatic dynamic kinetic resolution (DKR) via combined ruthenium and enzyme catalysis was used in the key step of a synthesis of a neonicotinoid pesticide derivative (S)-3. The DKR was carried out under mild conditions with low catalyst loading
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d32c4ed2677671d92c1e372662eb1873
https://doi.org/10.1021/jo9014276
https://doi.org/10.1021/jo9014276
Publikováno v:
ChemInform. 42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b8e35f9e5a0ead2e39779654e14f834
https://doi.org/10.1002/chin.201151030
https://doi.org/10.1002/chin.201151030
Publikováno v:
Chemistry-A European Journal
Enzyme- and ruthenium-catalyzed dynamic kinetic asymmetric transformation (DYKAT) of bicyclic diols to their diacetates was highly enantio- and diastereoselective to give the corresponding diacetates in high yield with high enantioselectivity (99.9 %
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22d4e2dbec223793424d9657f2eb7064
https://pubmed.ncbi.nlm.nih.gov/20196154
https://pubmed.ncbi.nlm.nih.gov/20196154
Publikováno v:
ChemInform. 38
Primary alcohols with an unfunctionalized stereogenic center in the β-position undergo an enzyme- and metal-catalyzed dynamic kinetic resolution (DKR). The in situ racemization of the primary alcohol, required for the DKR, takes place via: (i) ruthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31b58c33247fd64ea309470bcf6b963c
https://doi.org/10.1002/chin.200746060
https://doi.org/10.1002/chin.200746060
Publikováno v:
ChemInform. 38
An efficient method for the preparation of beta,gamma-unsaturated delta-lactones has been developed. The starting materials for the synthesis of these compounds are allene-substituted malonates which undergo gold-catalyzed cyclization by means of nuc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39bd754e808b1cd52740bf11362ef07e
https://doi.org/10.1002/chin.200739117
https://doi.org/10.1002/chin.200739117
Autor:
José Daniel Carballeira, Marco Bocola, Jan-Erling Bäckvall, Patrik Krumlinde, Manfred T. Reetz, Andreas Vogel
Publikováno v:
Chemical communications (Cambridge, England). (19)
Directed evolution of Pseudomonas aeruginosa lipase by the use of combinatorial active site saturation test (CAST) criteria provided a highly enantioselective mutant (Leu162Phe) for kinetic resolution of an axially chiral allene, p-nitrophenyl 4-cycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e36906c213ca3dad68c34c08366bee3
https://pubmed.ncbi.nlm.nih.gov/17695227
https://pubmed.ncbi.nlm.nih.gov/17695227
Publikováno v:
Journal of Organic Chemistry; 10/2/2009, Vol. 77 Issue 19, p7407-7410, 4p, 1 Graph