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S 4-nitro

S-[2-nitro-l-(2-thienyl)ethyl]-N-tert-butoxycorbonyl-L-cysteine (VII)... [Pg.1983]

The Newman-Kuart rearrangement is an example of a high-temperature reaction [34]. With the use of a microreactor, the reaction temperature could be extended up to 200 °C. 0-(2-Nitrophenyl)-N,N-dimethylthiocarbamate was converted to S-(2-nitro-phenyl)-N,N-dimethylcarbamothioate at 170 °C in 14 min at 90% yield. Quantitative conversion with a throughput of 34 g/h was achieved with sulfolane as solvent at the same temperature and reaction time. [Pg.235]

S-(2-Nitro-l-phenyl)ethyl, 678 S-2-(2,4-Dinitrophenyl)ethyl, 678 S-2-(4 -Pyridyl)ethyl, 679 S-2-Cyanoethyl, 679 S-2-(Trimethylsilyl)ethyl, 680 S-2,2-Bis(carboethoxy)ethyl, 681 S- (1-w -N itrophenyl-2- benzoyl) ethyl, 681 S-2-Phenylsulfonylethyl, 681... [Pg.648]

S-(2-Nitro-l-phenyl)ethyl Thioether RSCH(C6H5)CH2N02 (Chart 7)... [Pg.678]

S-(2-nitro-pheny tester) 60% 2-Hydroxy-thiobenzoesdure-S-phenylester 52%... [Pg.861]

Dichlor-benzol-thio8ulfonB ure-(l ) S-[2-nitro-phenyleeter] 11II38. [Pg.613]

N-Methyl-N-phenyl-S-[2-nitro-4-m9thyl-phen l-tiiiohydroxylainiii IS 16. N-o-TolyI>S-[2-Atro-4>mathyl-pheiiyl]-thiohydronlamin IS 17. N-p-Tolyl-S-[2-iiltro-4-methyl-phenyl]. [Pg.873]

CnM.,N.( S 2 -Nitro- toluol-suUons ure- (4) [2.3.o-trinitro-4- tiiChty-aBilid] 13II 296. CuH P S N PhenyHT -[l-phMyI-1.2.4-tn asolyl-(5)J-thioliamstra 26II 77. [Pg.956]

C,]iHMAaGlN, S [2-Nitro-phenylmttoapto]-tria. [4-dimetbylamino-piMDyl -aneD> ohloiid 10 n 441. [Pg.1663]

S-[2-Nitro-phenyl]-N is(qpropyliden-thio liydroxylamin C1158. [Pg.1986]

C HjoNsOgS S- [2-Nitro-phenyl] N-ben liden thiohydroxylamin 111z2. S [4-Nitro-phenyl]-N-benzyliden-thio h3rdr( 7]aiDm 7 1122. o-Cyan-benzolsulfons uie-anilid 12, 571. p-Cyan-benzolsuUons ure-anilid 12, 572. teenzoleulfonyl-phenyl-eyanamid 1 577. Thiobenzoe8 ure-[4-nitio-aiiilid] 12II391. [Pg.2312]

S- (2-Nitro-J -carboxyphenyl) -6-mercaptopurine Riboside. 5,5 -Dithio-bis-(2-nitrobenzoic acid) (DTNB, Ellman s reagent) 3.96 g (10 mmoles)... [Pg.291]

N-Methylmorpholine added with stirring to N- m-butoxycarbonyl-L-cysteine and / -nitrostyrene in anhydrous, Ng-satd. ethanol, and the product isolated after 10 min. N-methylmorpholinium N-tert-butoxycarbonyl-S-(2-nitro-l-phenethyl-L-cysteinate. Y 70%. G. Jung, H. Fouad, and G. Heusel, Ang. Ch. 87, 876 (1975). [Pg.435]

See other pages where S 4-nitro is mentioned: [Pg.455]    [Pg.534]    [Pg.143]    [Pg.246]    [Pg.2427]    [Pg.998]    [Pg.998]    [Pg.998]    [Pg.998]    [Pg.1110]    [Pg.5]    [Pg.463]    [Pg.743]    [Pg.772]    [Pg.964]    [Pg.1063]    [Pg.338]    [Pg.98]    [Pg.631]    [Pg.1026]    [Pg.1028]    [Pg.1502]    [Pg.1808]    [Pg.1850]    [Pg.1987]    [Pg.2077]    [Pg.2227]    [Pg.240]    [Pg.244]    [Pg.1652]   
See also in sourсe #XX -- [ Pg.15 , Pg.30 ]



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Nitro groups s. a. under Replacement)

S-3-Nitro-2-pyridinesulfenyl sulfide

S-Nitro-2-acetylaminonaphthalene

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