بحث البنية الفرعية

CCOC(=O)N1c2ccccc2C=CC1OCC

CC(C)Nc1nc(Cl)nc(N2CC3CCC(C2)O3)c1NC(=O)CCN(C)C

Reaction #162625

N-(4-(8-oxa-3-azabicyclo[3.2.1]octan-3-yl)-2-chloro-6-(isopropylamino)pyrimidin-5-yl)-3-(dimethylamino)propanamide

DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)NNC(=O)c1cnc2[nH]ccc2c1N1CCN(C(=O)OC(C)(C)C)CC1

Reaction #166743

tert-butyl 4-(5-(2-acetylhydrazinecarbonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazine-1-carboxylate

المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)NNC(=O)c1cnc2[nH]ccc2c1N1CCN(C(=O)OC(C)(C)C)CC1

Reaction #166759

tert-butyl 4-(5-(2-acetylhydrazinecarbonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazine-1-carboxylate

المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1

O=C(Nc1ccc(N2CCOCC2=O)cc1)C1CC(O)CN1C(=O)Cc1ccc(Cl)cc1

Reaction #184265

DOI: 10.1039/C8SC04228D

CCOC(=O)Nc1ccc(C(=O)NNC(=O)CSCCOc2ccccc2)cc1

Reaction #185127

DOI: 10.1039/C8SC04228D

COC(=O)c1ccc(C(=O)NN)cn1

Reaction #190419

DOI: 10.1039/C8SC04228D

CC1(C)OC2C(C(=O)NNC(=O)C(C)(C)C)OC(n3cnc4c(Cl)ncnc43)C2O1

Reaction #197237

DOI: 10.1039/C8SC04228D

NC(=O)c1c(-c2cnccn2)ssc1=S

Reaction #203994

DOI: 10.1039/C8SC04228D

c1ccc2c(c1)oc1ccccc12

Reaction #215695

DOI: 10.6084/m9.figshare.5104873.v1

$CC/C=C(\C)C(=O)N1C(=O)OC[C@@H]1c1ccccc1$

Reaction #219831

titled compound

المردود 89.2%DOI: 10.6084/m9.figshare.5104873.v1

$CCC/C=C(\C)C(=O)N1C(=O)O[C@H](c2ccccc2)[C@@H]1c1ccccc1$

Reaction #219839

titled compound

المردود 94.7%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)N1CCCC1C(=O)Nc1ccc(Cl)cc1

Reaction #260937

DOI: 10.1039/C8SC04228D

NN(C(=O)COCCCOc1ccccc1)C(=O)c1ccc(O)cc1

Reaction #262847

DOI: 10.1039/C8SC04228D

COC1CC(C(=O)Nc2ccc(N3CCCCC3=O)cc2F)N(C(=O)OC(C)(C)C)C1

Reaction #267013

DOI: 10.1039/C8SC04228D

CC(C)(C)OC(=O)N1CCC[C@H]1C(=O)Nc1ccccc1

Reaction #313421

BOC-proline anilide

المردود 129.3%DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)NCCSC1CC(=O)OC1(C(=O)OCc1ccc([N+](=O)[O-])cc1)N1OC[C@H](NC(=O)Cc2ccccc2)C1=O

Reaction #319401

subject Compound ( 71 )

المردود 57.3%DOI: 10.6084/m9.figshare.5104873.v1

C=CCOC(=O)COc1cccc(NC(=O)[C@@H]2C[C@H](SC(C)=O)CN2C(=O)OCC=C)c1

Reaction #347492

المردود 111.5%DOI: 10.6084/m9.figshare.5104873.v1

C=CCOC(=O)c1cccc(NC(=O)[C@@H]2C[C@H](SC(C)=O)CN2C(=O)OCC=C)c1

Reaction #354025

(2S,4S)-4-acetylthio-1-allyloxycarbonyl-2-(3-allyloxycarbonylphenylcarbamoyl)pyrrolidine

المردود 101.1%DOI: 10.6084/m9.figshare.5104873.v1

C=CCOC(=O)c1cccc(NC(=O)[C@@H]2C[C@H](SC(C)=O)CN2C(=O)OCc2ccc([N+](=O)[O-])cc2)c1

Reaction #354028

(2S,4S)-4-acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-(3-allyloxycarbonylphenylcarbamoyl)pyrrolidine

المردود 85.6%DOI: 10.6084/m9.figshare.5104873.v1

CCCCCCCCCCCCCC(=O)O[C@H](CCCCCCCCCCC)CC(=O)NC(=O)[C@@H](N)CO

Reaction #364780

N-[(R)-3-tetradecanoyloxytetradecanoyl]-L -serinamide

المردود 71.3%DOI: 10.6084/m9.figshare.5104873.v1

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