7-Amino-7-carboxy

Amino-, carboxy- and endo peptidase which cleave peptides at specific amino acid linkages... 

COOH Zn NH3 konz. 3 h, 50° 2- ( Amino-carboxy-methyl) -5-carboxymethyl- 50 171-172 l... 

Amino-carboxy-methyl )-2-methyl-. [bzw. -2,4-dimethyl-... bzw. 2-methyl-4-phenyl-...]-/, 2-oxazol (X = H, CH CSHS)... 

L-CCG 1, selective group II mGluR agonist, 2-(Amino-carboxy-methyl)-cyclopropane-carboxylic acid... 

Curry, K. Novel amino carboxy alkyl derivatives of barbituric acid, WO 0179185. 

Scheme 3 Simple Amino, Carboxy, and Hydroxy Cores and Templates...

Covalent binding of amino, carboxy, and nitro-substituted aminopropyltriethoxysilanes to oxidized silicon surfaces and their interaction with octadecanamine and octadecanoic acid studied by X-ray photoelectron spectroscopy and ellipsometry... 

Keywords Silanization silanes (amino, carboxy, and nitro-alkyl functionalized) adhesion ocia-decanoic acid octadecanamine X-ray photoelectron spectroscopy ellipsometry. 

Page 238, lines 10 and 11. For amino-carboxy-deoxynonuloses read aminocarboxydideoxyoctuloses. ... 

There is a separate table for each class of pyrazine with one type of substituent, a table for each combination containing two types of substituents, and appropriate tables for three and four types of substituents. Thus, for example, 2-amino-3-ethoxypyrazine is listed in Table A. 12 (amino oxypyrazines), 3-amino-2-methoxy-carbonyl-5-methylsulfinylpyrazine in Table A. 16 (amino carboxy sulfonylpyra-zines), and 2-amino-5-chloro-6-ethoxy-3-ethoxycarbonylpyrazine in Table A.20 (amino carboxy halogenopyrazines with other functional groups). 

TABLE A.20 AMINO-CARBOXY-HALOGENOPYRAZINES WITH OTHER FUNCTIONAL GROUPS... 

The silane crosslinker contains a wide range of reactive substituents e.g. amino-, carboxy-, carbonamido-, oxime-, carbonyl- and/or alkoxy-groups. 

Bei Trivialnamen von Verbindungen aus zwei verschiedenen Aminosauren wird die Konfiguration des a-C-Atoms der kiirzeren Aminosaure zur Bezeichnung beniitzt (z. B. D-Cystathionin fur S-D-jJ-Amino- -carboxy-athyl-L-hcmccystein). 

Intramolecular cyclisation of A-substituted phthalimides continues to attract interest. Product formation from a series of A-phthaloylcysteine derivatives (141) has been shown to be multiplicity dependent. y-Hydrogen abstraction occurs predominantly from the singlet excited state to yield products derived from the intermediate azetidine (140). In contrast, triplet excited (141) initiates SET from the sidechain sulfur to the excited carbonyl. Deprotonation at the s-carbon and cyclisation produces thiazinoisoindoles (142). A -Phthalimido-co-amino carboxy-... 

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