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Methansulfonic acid

Holmes AJ, DP Kelly, SC Baker, AS Thompson, P de Marco, EM Kenna, JC Murrell (1997) Methylosulfonomonas methylovora gen. nov., sp. nov., and Marinosulfonomonas methylotropha gen. nov., sp. nov. novel methylotrophs able to grow on methansulfonic acid. Arch Microbiol 167 46-53. [Pg.591]

Thompson AS, NJP Owens, JC Murrell (1995) isolation and characterization of methansulfonic acid-degrading bacteria from the marine environment. Appl Environ Microbiol 61 2388-2393. [Pg.592]

Rgts Methansulfonic Acid Anhydride L-2-amino-l-propanol DMF... [Pg.75]

The proposed [45b] radical mechanism for the formation of methansulfonic acid in the 820 initiated reaction involves the steps of initiation... [Pg.340]

MOPITT measurement of pollution in the troposphere MSA methansulfonic acid... [Pg.591]

Positive-ions MALDI-TOF mass spectra of Ny6 samples (a) reacted with diaminohexamethyl-ene (b) reacted with decylamine (c) reacted with adipic acid (d) hydrolyzed with water in methansulfonic acid. (Continued)... [Pg.465]

The MAFDI spectrum of Nys hydrolyzed in aqueous methansulfonic acid (Figure 10.20d) is dominated by a series of intense peaks corresponding to sodiated ions of the Nys oligomers with NH2/COOH end-groups (peaks 4). Protonated (peaks 5) and potassiated (peaks 6) ions of these oligomers appear with low intensity. [Pg.467]

Reaction with Hydrates ofa-Keto Aldehydes and Glyoxylates. Catalytic allylations of the hydrates of a-keto aldehydes and glyoxylates with allyltrimethylsilane can be performed by using Yb(OTf)3 and Sc(OTf)3 (eq 26). TMSOMs, which is formed in situ from methansulfonic acid and allyltrimethylsilane, is also a viable catalyst for this reaction. ... [Pg.17]

The first manufacturing route of the GEM side-chain relied on a-cyanoketone 125 however, the number of chemical steps from 125 to the final side-chain was reduced by one step (Noh et ah, 2004a). The sequence began with a selective hydrogenation with Raney nickel followed by double bond migration to enamine 131 (Scheme 4.25). The amino functionality of 131 was then monoprotected, and the double bond was reduced under hydrogenation conditions to afford pyrrolidine-3-one 133. Treatment of 133 with methoxylamine yielded methoxyoxime 129. Deprotection of the carbamate functionality was achieved with methanesulfonic acid to afford the C7-side-chain as the bis-methansulfonate salt. [Pg.62]

SYNS EMS ENT 26,396 ETHYL ESTER of METHANESULFONIC ACID ETHYL ESTER of METHYLSL LFONIC ACID ETHYL ESTER of METHYLSULPHONICACID ETHYL METHANE-SULPHONATE ETHYL METHANSULFONATE ETHYL METHANSULPHONATE HALF-MYLERAN METHYNESULPHONIC ACID ETHYL ESTER METHYLSULFONIC ACID, ETHYL ESTER NSC-26805 RCRA I tYISTE NUMBER U119... [Pg.637]

SYNS as-DLMETHYL SULPHATE METHANE-SULPHONTC ACID METHYL ESTER METHYL ESTER of METHANESULFONIC ACID METHYL ESTER of METHANESULPHONIC ACID METHYL METHANE-SULFONATE n METHYL METHANESULPHONATE METHYL METHANSULFONAT (GERMAN) METHYL METHANSULFONATE METHYL METHANSULPHON-ATE MMS NSC-50256... [Pg.933]

Synonyms as-Dimethyl sulfite Methanesulfonic acid, methyl ester Methyl ester of methanesulfonic acid Methyl mesylate Methyl methansulfonate MMS... [Pg.2654]

See other pages where Methansulfonic acid is mentioned: [Pg.118]    [Pg.222]    [Pg.659]    [Pg.118]    [Pg.396]    [Pg.135]    [Pg.104]    [Pg.118]    [Pg.222]    [Pg.659]    [Pg.118]    [Pg.396]    [Pg.135]    [Pg.104]    [Pg.289]    [Pg.614]    [Pg.700]   
See also in sourсe #XX -- [ Pg.383 ]



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