부분 구조 검색

C#CCO

C#CCOCN(OC)C(=O)OC
Reaction #3499
methyl N-methoxy-N-propargyloxymethylcarbamate
수율 75.9%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(C)(O)CCC=C(C)CCC=C(C)COC(C)=O
Reaction #5756
3,7,11-trimethyl-12-acetoxy-6,10-dodecadien-1-in-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccccc1C#CC(C)(C)O
Reaction #42159
4-(N,N-dimethylaminophenyl)-2-methyl-3-butyne-2-ol
수율 86.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccccc1C#CC(C)(C)O
Reaction #42178
4-(N,N-dimethylaminophenyl)-2-methyl-3-butyne-2-ol
수율 86.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOCO[C@H]1CC[C@@]2(C)[C@H](CC[C@@H]3[C@@H]2CC[C@]2(C)C(O)(CCC(=O)O)CC[C@]32O)C1
Reaction #50277
17-hydroxy-17-(2-carboxyethyl)-3beta-ethoxymethoxy-14-hydroxy-5beta,14beta-androstane
DOI: 10.6084/m9.figshare.5104873.v1
C#CC(C)(COc1ccccc1)O[Si](C)(C)C
Reaction #54548
3-methyl-3-trimethylsilyloxy-4-phenoxy-1-butyne
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
COC(=O)CCCC#CC(O)C1C(=O)C=CC1C=CC(O)C1CCCC1
Reaction #63768
4-(3-hydroxy-3-cyclopentyl-1-propenyl)-5-(1-hydroxy-6-methoxycarbonyl-2-hexyn-yl)-2-cyclopentenone
수율 79.3%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
수율 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
수율 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
수율 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
수율 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#CCOCN(OC)C(=O)OC
Reaction #202765
DOI: 10.1039/C8SC04228D
C#CCOc1ccc(C(=O)NC(C)C(C)(C)C)cc1F
Reaction #206393
DOI: 10.1039/C8SC04228D
Cc1cccc(OCC#CCC#CCC#CCC#CCCCC(=O)O)c1
Reaction #208062
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(COCC#CC(=O)O)NC(C)=C(C(=O)OC)C1c1cccc(Cl)c1Cl
Reaction #210664
DOI: 10.1039/C8SC04228D
CCC[CH2][Sn]([CH]=CC(COc1ccc(F)cc1)O[Si](C)(C)C)([CH2]CCC)[CH2]CCC
Reaction #213306
DOI: 10.1039/C8SC04228D
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