TW466255B - Photoactivatable nitrogen-contained bases on Α-amino alkenes - Google Patents

Info

Publication number

TW466255B

TW466255B TW087105322A TW87105322A TW466255B TW 466255 B TW466255 B TW 466255B TW 087105322 A TW087105322 A TW 087105322A TW 87105322 A TW87105322 A TW 87105322A TW 466255 B TW466255 B TW 466255B

Authority

TW

Taiwan

Prior art keywords

group

alkyl

patent application

page

cns

Prior art date

1997-03-18

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• 239000000203 mixture Substances 0.000 claims abstract description 47
• 238000006243 chemical reaction Methods 0.000 claims abstract description 29
• 238000000034 method Methods 0.000 claims abstract description 23
• 125000003118 aryl group Chemical group 0.000 claims abstract description 17
• 238000006555 catalytic reaction Methods 0.000 claims abstract description 9
• 150000002894 organic compounds Chemical class 0.000 claims abstract description 8
• -1 fluorene compound Chemical class 0.000 claims description 200
• 125000000217 alkyl group Chemical group 0.000 claims description 43
• 229910052739 hydrogen Inorganic materials 0.000 claims description 28
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 28
• 229920000642 polymer Polymers 0.000 claims description 28
• 238000000576 coating method Methods 0.000 claims description 27
• 239000001257 hydrogen Substances 0.000 claims description 24
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 21
• NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims description 19
• 239000011248 coating agent Substances 0.000 claims description 18
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 15
• 150000002367 halogens Chemical class 0.000 claims description 13
• 229920000647 polyepoxide Polymers 0.000 claims description 13
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• 125000001624 naphthyl group Chemical group 0.000 claims description 10
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• 125000000304 alkynyl group Chemical group 0.000 claims description 9
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• JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims 1
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• 125000001931 aliphatic group Chemical group 0.000 claims 1
• 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims 1
• 229910052797 bismuth Inorganic materials 0.000 claims 1
• JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims 1
• HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol group Chemical group [C@@H]1(CC[C@H]2[C@@H]3CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)[C@H](C)CCCC(C)C HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims 1
• 239000000385 dialysis solution Substances 0.000 claims 1
• POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 claims 1
• 229910052735 hafnium Inorganic materials 0.000 claims 1
• VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims 1
• 125000001188 haloalkyl group Chemical group 0.000 claims 1
• 238000010438 heat treatment Methods 0.000 claims 1
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• 239000011975 tartaric acid Substances 0.000 claims 1
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
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