部分構造検索

CCOCCl

[N-]=[N+]=NCc1ccc(C(=N)NC(=O)OCc2ccccc2)cc1
Reaction #952
4-(benzyloxycarbonylamidino) benzyl azide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCCCC1
Reaction #1172
N-Cbz-piperidine
収率 59.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1282
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1Cc2ccccc2C[C@H](NC(=O)OCc2ccccc2)C1=O
Reaction #1414
(S)-1,3,4,5-Tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CCN(C(=O)OCc2ccccc2)N1
Reaction #1426
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC=C4C[C@](O)(C(=O)OCCl)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #1502
3-(Chloromethoxycarbonyl) Cholesterol
DOI: 10.6084/m9.figshare.5104873.v1
ClCOCC[Se]c1ccccc1
Reaction #1651
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CN1C(=O)[C@@H](CC(=O)OCOC(=O)C(C)(C)C)O[C@H](c2ccccc2Cl)c2cc(Cl)ccc21
Reaction #1867
trans-7-chloro-5-(2-chlorophenyl)-1-isobutyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetic acid pivaloyloxymethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1(c2ccccc2)CCN(CCOC(CN(C)C(=O)OCc2ccccc2)c2ccc(Cl)c(Cl)c2)CC1.Cl
Reaction #1938
hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](OC(=O)OCc3ccccc3)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #2079
3β-benzyloxycarbonyloxy-5-androsten-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOCn1c(=O)c2c(ncn2Cc2ccccc2)n(C)c1=O
Reaction #2092
7-Benzyl-1-ethoxymethyl-3-methylxanthine
DOI: 10.6084/m9.figshare.5104873.v1
C#CCOCN(OC)C(=O)OC
Reaction #3499
methyl N-methoxy-N-propargyloxymethylcarbamate
収率 75.9%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOCN(OC)C(=O)c1ccccc1
Reaction #3502
N-methoxy-N-propargyloxymethylbenzamide
収率 91.9%DOI: 10.6084/m9.figshare.5104873.v1
C#CCOCN(OC)S(=O)(=O)c1ccccc1
Reaction #3503
N-methoxy-N-propargyloxymethylbenzenesulfonamide
収率 85.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(Cc1cccs1)C(=O)O)OCc1ccccc1
Reaction #3768
N-(Benzyloxycarbonyl) β-thienyl-D,L-alanine
収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc[n+](COC(=O)c2ccccc2)c1.[Cl-]
Reaction #4813
1-benzoyloxymethyl-3-carboethoxypyridinium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)OC[n+]1ccn(C)c1.[Cl-]
Reaction #4815
1-n-Dodecanoyloxymethyl-3-Methylimidazolium Chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC(=O)OC[N+]12CCC(CC1)CC2.[Cl-]
Reaction #4816
n-Dodecanoyloxymethylquinuclidinium Chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC[n+]1ccccc1)c1ccccc1.[Cl-]
Reaction #4817
Benzoyloxymethylpyridinium Chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCN(C(=O)[C@H](Cc2ccc(O)cc2)NS(=O)(=O)c2cccc3cnccc23)CC1
Reaction #5817
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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