بحث البنية الفرعية

30547

Cc1ccc(NC(=O)c2ccc(CN3CC[C@H](NC(=O)OC(C)(C)C)C3=O)c(C(F)(F)F)c2)cc1Nc1nccc(-c2cncnc2)n1
Reaction #42071
objective compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCNC(=O)OC(C)(C)C)OP(=O)(OC)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #58021
2-[(1-benzyloxycarbonylamino-2-methyl-propyl)-methoxy-phosphinoyloxy]-5-tert-butoxycarbonylamino-pentanoic acid methyl ester
المردود 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CNC(=O)c2ccc(C(C)=O)cc2)c1
Reaction #60017
(4-acetylphenyl)-N-[(3-methoxyphenyl)methyl]carboxamide
المردود 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)ccc1Nc1c(C(=O)NOCC2CC2)cc2nc[nH]c2c1F
Reaction #60245
pure desired product
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCn1cnc2c(F)c(Nc3ccc(Br)cc3C)c(C(=O)NOCC3CC3)cc21
Reaction #60265
pure desired product
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(CNC(=O)c2cc3cc(F)cc(Br)c3[nH]2)c1
Reaction #60609
6
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccoc1C(N)=O
Reaction #60873
title compound
المردود 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)OP(=O)(CC=CCC(CC(C)=CCc1c(OC)c(C)c2c(c1OCC[Si](C)(C)C)C(=O)OC2)C(=O)OCC[Si](C)(C)C)OC
Reaction #61238
desired product
المردود 74.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)OP(=O)(COCC(C)=CCc1c(O)c2c(c(C)c1OC)COC2=O)Oc1ccccc1
Reaction #61253
desired product
المردود 34.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)OP(=O)(CC(C)=CCc1c(OC)c(C)c2c(c1OCC[Si](C)(C)C)C(=O)OC2)Oc1ccccc1
Reaction #61297
desired product
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)OP(=O)(CC=CCC(CC(C)=CCc1c(OC)c(C)c2c(c1OCC[Si](C)(C)C)C(=O)OC2)C(=O)OCC[Si](C)(C)C)OC
Reaction #61902
desired product
المردود 74.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)OP(=O)(COCC(C)=CCc1c(O)c2c(c(C)c1OC)COC2=O)Oc1ccccc1
Reaction #61917
desired product
المردود 34.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)OP(=O)(CC(C)=CCc1c(OC)c(C)c2c(c1OCC[Si](C)(C)C)C(=O)OC2)Oc1ccccc1
Reaction #61961
desired product
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(NC(=O)NS(=O)(=O)c2ccc(Cl)s2)ccc1NCc1ccccc1
Reaction #66428
{[(5-chloro(2-thienyl))sulfonyl]amino}-N-{3-methyl-4-[benzylamino]phenyl}carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)Nc2ccccc2)cc1)NS(=O)(=O)c1ccc(Cl)s1
Reaction #66430
{[(5-chloro(2-thienyl))sulfonyl]amino}-N-[4-(N-phenylcarbamoyl)phenyl]carboxamide
المردود 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1cc(OC)cc2c1ccc(=O)n2CCN1CCC(N(Cc2ccc3c(c2)OCCO3)C(=O)OC(C)(C)C)CC1
Reaction #68142
tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(7-methoxy-5-((methylamino)carbonyl)-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate
المردود 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)COc1cccc2c1ccc(=O)n2CCN1CCC(N(Cc2ccc3c(c2)OCCO3)C(=O)OC(C)(C)C)CC1
Reaction #68205
tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(5-((methylamino)carbonylmethyloxy)-2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1C[C@@H](C(=O)N[C@H](C(=O)O)C(C)C)C[C@@H]1O[N+](=O)[O-]
Reaction #69439
title compound
المردود 90.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(NC(=O)C1CC2CCCCC2N1C(=O)C(NC(=O)C(NC(=O)c1cnccn1)C1CCCCC1)C(C)(C)C)C(O)C(=O)OCC
Reaction #70196
32
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2cc(Oc3ncnc4c3CCN(C(=O)OC(C)(C)C)C4)ccc2[nH]1
Reaction #73348
title compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي