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Morin reaction

Color reactions are more or less clearly defined reactions of the substances with suitable reagents. Substance-specific reactions are not usually available, e. g. many compounds with aromatic skeletons give both a positive Vitali-Morin reaction [1 -4] and a positive Marquis reaction [4]. Again, numerous aldehydes react with electron-rich compounds in acidic medium to yield colored substances (cf. Chapters 2 and 3.1). [Pg.36]

Conversion of semisynthetic penicillins, e.g. 9, into 7-acylamino-3-methyl-8 oxoceph-3-em-4-carboxylic ester 12 (penicillin rearrangement, Morin reaction 1969) [135]. [Pg.391]

Morin reaction. The dried chromatograms are sprayed with a 0.05% solution of morin (3,5,7,2 ,4-pentahydroxy flavone) in methanol, and heated for 2 min at 100°C. The N-protected amino... [Pg.435]

Methaemoglobin 555 Methaqualon 498 Methotrexat 490 Methoxatin 406,613 2-Methoxyazocine 547 Methylene Blue 447 Methyloxiran 24 Methylphenobarbital 473 l-Methylpyrrolidin-2-one 160 Methylreticulol 588 Metribuzin 508 Metronidazole 228 Mitomycin 36 Mobam 103 Monensin 89 Morin reaction 456 Morpholine 447,448 Mtinchnone 175 Murrayanine 149 Muscaflavin 539 Muscarine 88 Muscimol 190 Muscone 100... [Pg.626]

Madelung synthesis (indole) 137 Marckwald cleavage, of furans 79 Marckwald synthesis (imidazole) 224 Meth-Cohn synthesis (quinoline) 402 Meyer s oxazoline method 183 Morin reaction 456 Mukaiyama reaction 380 Mukaiyama reagents 53, 380... [Pg.631]

Photooxidation of the dGuo-5 -lysine ester leads to Z cross-linked to the lysine moiety (Morin and Cadet 1995), indicating that DNA-protein cross-links may also occur via such a process in case this amino acid happens to be in a proper position for the reaction to proceed. [Pg.308]

Moorthy PN, Hayon E (1975) Free-radical intermediates produced from the one-electron reduction of purine, adenine and guanine derivatives in water. J Am Chem Soc 97 3345-3350 Mori M, Teshima S-l, Yoshimoto H, Fujita S-l, Taniguchi R, Hatta H, Nishimoto S-l (2001) OH Radical reaction of 5-substituted uracils pulse radiolysis and product studies of a common redox-ambivalent radical produced by elimination of the 5-substituents. J Phys Chem B 105 2070-2078 Morin B, Cadet J (1995) Chemical aspects of the benzophenone-photosensitized formation of two lysine - 2 -deoxyguanosine cross-links. J Am Chem Soc 117 12408-12415 Morita H, Kwiatkowski JS,TempczykA(1981) Electronic structures of uracil and its anions. Bull Chem Soc Jpn 54 1797-1801... [Pg.324]

Baranac, J. M., Petranovic, N. A., Dimitric-Markovic, J. M. (1997b). Spectrophotometric study of anthocyan copigmentation reactions.3. Malvin and the nonglycosidized flavone morin. J. Agric. Food Chem., 45, 1698-1700. [Pg.561]


See other pages where Morin reaction is mentioned: [Pg.69]    [Pg.127]    [Pg.732]    [Pg.49]    [Pg.50]    [Pg.51]    [Pg.1979]    [Pg.471]    [Pg.599]    [Pg.459]    [Pg.69]    [Pg.127]    [Pg.732]    [Pg.49]    [Pg.50]    [Pg.51]    [Pg.1979]    [Pg.471]    [Pg.599]    [Pg.459]    [Pg.293]    [Pg.504]    [Pg.91]    [Pg.322]    [Pg.328]    [Pg.65]    [Pg.67]    [Pg.83]    [Pg.83]    [Pg.215]    [Pg.215]    [Pg.197]    [Pg.390]    [Pg.293]    [Pg.293]    [Pg.552]    [Pg.661]    [Pg.456]    [Pg.490]    [Pg.314]    [Pg.398]    [Pg.468]    [Pg.313]    [Pg.191]    [Pg.119]   
See also in sourсe #XX -- [ Pg.391 ]




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Morine

Vitali-Morin reaction

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