بحث البنية الفرعية

496102

C#CCOCN(OC)C(=O)OC
Reaction #3499
methyl N-methoxy-N-propargyloxymethylcarbamate
المردود 75.9%DOI: 10.6084/m9.figshare.5104873.v1
OC1(C#CCOC2CCCCO2)CCOCC1
Reaction #50176
4-hydroxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran
المردود 88.3%DOI: 10.6084/m9.figshare.5104873.v1
COC1(C#CCOC2CCCCO2)CCOCC1
Reaction #50177
4-methoxy-4-[3-(tetrahydropyran-2-yloxy)prop-1-ynyl]tetrahydropyran
المردود 96.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1cccc(OC)c1)n1ccc2cc(OCCc3ccc4c(n3)N(C(=O)OC(C)(C)C)CCC4)ccc21
Reaction #52292
title compound
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1ccccc1)n1ccc2cc(OCCc3cccc(N(C)C(=O)OC(C)(C)C)n3)ccc21
Reaction #52312
title compound
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=C(c1ccccc1)n1ccc2cc(CCCc3ccc4cccnc4n3)ccc21
Reaction #52325
title product
المردود 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCOc1ccc2c(c1)C(C#CC1CC1)(C(F)(F)F)OC(=O)N2
Reaction #57294
11
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCOc1ccc2c(c1)C(C#CC1CC1)(C(F)(F)F)OC(=O)N2)ON1C(=O)CCC1=O
Reaction #57295
12
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1ccc2c(c1)sc1nc(=O)cc(-c3ccccc3)n12
Reaction #62812
ethyl 2-oxo-4-phenyl-2H-pyrimido[2,1-b]benzothiazole-8-acetate
المردود 26.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(OC(=O)C(c1cnc(C(C)(C)C)nc1)C(C)C)c1cccc(Oc2ccccc2)c1
Reaction #62877
(RS)-1-ethynyl-1-(3-phenoxyphenyl)methyl (RS)-2-[2-(2-methylprop-2-yl)-pyrimidin-5-yl]-3-methylbutyrate
المردود 90.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1C#CC(=O)O)C(=O)c1c([nH]c3cc(C#N)ccc13)C2(C)C
Reaction #90067
title compound
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCO[C@H]1CC[C@@]2(C)C(CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCCC(C)CO)[C@@]4(C)CC[C@@H]32)C1
Reaction #162018
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@H](O[C@@H]2[C@H](OC(C)=O)[C@@H](O[C@@H]3[C@@H](OCCCn4cc(CO[C@H]5CC[C@@]6(C)C(CC[C@H]7[C@@H]8CC[C@H]([C@H](C)CCCC(C)C)[C@@]8(C)CC[C@@H]76)C5)nn4)O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@@H]3OC(C)=O)O[C@H](COC(C)=O)[C@H]2OC(C)=O)[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #162019
triazole
المردود 81.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](OCc5cn(CCCO[C@H]6O[C@H](COC(=O)c7ccccc7)[C@@H](OC(=O)c7ccccc7)[C@H](O[C@H]7O[C@H](COC(=O)c8ccccc8)[C@@H](OC(=O)c8ccccc8)[C@H](O[C@H]8O[C@H](COC(=O)c9ccccc9)[C@@H](OC(=O)c9ccccc9)[C@H](OC(=O)c9ccccc9)[C@@H]8OC(=O)c8ccccc8)[C@@H]7OC(=O)c7ccccc7)[C@@H]6OC(=O)c6ccccc6)nn5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #162024
triazole
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](n2cc(CO[C@H]3CC[C@@]4(C)C(CC[C@H]5[C@@H]6CC[C@H]([C@H](C)CCCC(C)C)[C@@]6(C)CC[C@@H]54)C3)nn2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1O[C@H]1O[C@H](COC(C)=O)[C@@H](O[C@H]2O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]2OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O
Reaction #162029
triazole
المردود 68.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC=CC#CCOC1CCCCO1
Reaction #176091
DOI: 10.1039/C8SC04228D
NS(=O)(=O)c1cccc(C#CCOCCCCCCCBr)c1
Reaction #183901
DOI: 10.1039/C8SC04228D
C#CCOc1cc(-c2cccc(F)c2F)ncn1
Reaction #184372
DOI: 10.1039/C8SC04228D
C#CCOCN(OC)C(=O)OC
Reaction #202765
DOI: 10.1039/C8SC04228D
COC(=O)C#CC(=O)c1ccc2c(c1)OCO2
Reaction #202930
DOI: 10.1039/C8SC04228D
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