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Galaverna, Gianni; Corradini, Roberto; Dossena, Arnaldo; Marchelli, Rosangela (1993). "Diaminomethane dihydrochloride, a novel reagent for the synthesis of primary amides of amino acids and peptides from active esters".
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Robert A. Smiley "Phenylene- and
Toluenediamines" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim.
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435:
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Xylylenediamines are classified as alkylamines since the amine is not directly attached to an aromatic ring.
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138:(diaminomethane) of theoretical interest only, but its hydrochloride can be used in the synthesis of amides.
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Karsten Eller; Erhard Henkes; Roland
Rossbacher; Hartmut Höke (2005). "Amines, Aliphatic".
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112:(1,2-diamines) are a structural motif in many biological compounds and are used as
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145:(1,2-diaminoethane). Related derivatives include the N-alkylated compounds,
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10.1002/(SICI)1521-3773(19981016)37:19<2580::AID-ANIE2580>3.0.CO;2-L
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Various N-methylated derivatives of the phenylenediamines are known:
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is related to PPD but contains a methyl group on the ring.
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Examples with two aromatic rings include derivatives of
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6 carbons: hexamethylenediamine (hexane-1,6-diamine),
516:
International
Journal of Peptide and Protein Research
492:Lucet, D., Le Gall, T. and Mioskowski, C. (1998),
584:
462:Ullmann's Encyclopedia of Industrial Chemistry
235:Derivatives of ethylenediamine are prominent:
26:General structure of (primary) diamines. The
93:diamines, as those are the most reactive.
570:at the U.S. National Library of Medicine
496:. Angew. Chem. Int. Ed., 37: 2580–2627.
42:R is a divalent organic radical (e.g. a
585:
258:, two diastereomers, one of which is C
248:, two diastereomers, one of which is C
123:
393:N,N'-di-2-butyl-1,4-phenylenediamine
323:
292:
13:
528:10.1111/j.1399-3011.1993.tb00349.x
436:"Nucleophilicity Trends of Amines"
14:
609:
561:
494:The Chemistry of Vicinal Diamines
104:) is most important, followed by
96:In terms of quantities produced,
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280:
208:
171:
19:
159:tetrakis(dimethylamino)ethylene
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428:
1:
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225:trimethylhexamethylenediamine
17:
15:
7:
387:dimethyl-4-phenylenediamine
230:
151:1,2-dimethylethylenediamine
147:1,1-dimethylethylenediamine
10:
614:
266:
128:
572:Medical Subject Headings
554:10.1002/14356007.a19_405
470:10.1002/14356007.a02_001
440:Master Organic Chemistry
464:. Weinheim: Wiley-VCH.
319:-xylylenediamine or PXD
304:-xylylenediamine or OXD
246:diphenylethylenediamine
69:. Diamines are used as
417:1,8-diaminonaphthalene
256:1,2-diaminocyclohexane
118:coordination chemistry
578:Synthesis of diamines
287:1,4-Diazacycloheptane
273:1,4-Diazacycloheptane
202:(pentane-1,5-diamine)
188:(propane-1,3-diamine)
412:4,4'-diaminobiphenyl
195:(butane-1,4-diamine)
377:p-phenylenediamine
362:2,5-diaminotoluene
242:, which is chiral.
240:1,2-diaminopropane
186:1,3-diaminopropane
124:Aliphatic diamines
395:, an antioxidant.
358:-phenylenediamine
349:-phenylenediamine
340:-phenylenediamine
330:phenylenediamines
324:Aromatic diamines
98:1,6-diaminohexane
89:refers mostly to
65:with exactly two
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311:-xylylenediamine
293:Xylylenediamines
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136:methylenediamine
110:Vicinal diamines
100:(a precursor to
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30:amino groups (NH
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178:Ethylenediamine
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143:ethylenediamine
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106:ethylenediamine
48:phenylene group
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444:. Retrieved
442:. 2018-05-07
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389:, a reagent.
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67:amino groups
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405:naphthalene
332:are known:
262:-symmetric.
252:-symmetric.
198:5 carbons:
191:4 carbons:
184:3 carbons:
141:2 carbons:
85:. The term
73:to prepare
587:Categories
446:2019-08-18
423:References
216:Cadaverine
200:cadaverine
193:putrescine
155:ethambutol
134:1 carbon:
79:polyimides
75:polyamides
536:0367-8377
102:Nylon 6-6
83:polyureas
598:Monomers
593:Diamines
568:Diamines
401:biphenyl
360:or PPD.
231:Branched
71:monomers
114:ligands
91:primary
87:diamine
59:diamine
28:primary
574:(MeSH)
534:
476:
351:or MPD
342:or OPD
328:Three
313:or MXD
267:Cyclic
129:Linear
81:, and
61:is an
163:TMEDA
63:amine
532:ISSN
474:ISBN
403:and
44:para
37:blue
550:doi
524:doi
498:doi
466:doi
116:in
589::
530:.
520:42
518:.
472:.
438:.
407::
161:,
157:,
153:,
149:,
120:.
108:.
77:,
57:A
50:).
552::
538:.
526::
500::
482:.
468::
449:.
356:p
347:m
338:o
317:p
309:m
302:o
260:2
250:2
165:.
46:-
40:,
32:2
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
