بحث البنية الفرعية

8549

COC(=O)C(Cc1ccc2ccccc2c1)N1CCN(S(=O)(=O)c2ccccc2[N+](=O)[O-])C(CCCNC(=O)OCc2ccccc2)C1=O
Reaction #8624
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(SCCO)c([N+](=O)[O-])c1
Reaction #49954
2-[2,4-dinitrophenylsulfanyl]ethanol
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)c1ccc(F)cc1[N+](=O)[O-]
Reaction #53737
4-fluoro-1-methylsulfinyl-2-nitrobenzene
المردود 63.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CO[C@](C)(C(N)=O)C(F)(F)F)(NS(=O)(=O)c1ccccc1[N+](=O)[O-])c1cc(Br)ccc1F
Reaction #67513
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC1(Br)C=CC=CC1SCCCCl
Reaction #79278
1-bromo-2-[(3-chloropropyl)thio]-benzenamine
المردود 93.2%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1S(=O)(=O)N(CCCn1c2ccc(Br)cc2c2cc(Br)ccc21)c1ccccc1
Reaction #90432
white solid
المردود 35.5%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)c1cc(Br)ccc1n2CCCNc1ccccc1
Reaction #90433
colorless oil
المردود 60.9%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1S(=O)(=O)N(CCCn1c2ccc(Br)cc2c2cc(Br)ccc21)c1ccccc1
Reaction #90468
white solid
المردود 35.5%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc2c(c1)c1cc(Br)ccc1n2CCCNc1ccccc1
Reaction #90469
colorless oil
المردود 60.9%DOI: 10.6084/m9.figshare.5104873.v1
CNC[C@H](NC(=O)c1c(C)nc2c(OCC3CCCCC3)cccn12)c1ccccc1
Reaction #92761
8-(cyclohexylmethoxy)-2-methyl-N-[(1R)-2-(methylamino)-1-phenylethyl]imidazo[1,2-a]pyridine-3-carboxamide
المردود 57.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(C)c3c(-c4nc5c(c(N6CCN(S(=O)(=O)c7ccccc7[N+](=O)[O-])[C@H](C)C6)n4)CN(Cc4ccccc4)CC5)cccc32)cc1
Reaction #167990
(R)-6-benzyl-2-(3-methyl-1-tosyl-1H-indol-4-yl)-4-(3-methyl-4-((2-nitrophenyl)sulfonyl)piperazin-1-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(C)c3c(-c4nc5c(c(N6CCN(S(=O)(=O)c7ccccc7[N+](=O)[O-])[C@H](C)C6)n4)CNCC5)cccc32)cc1
Reaction #167991
(R)-2-(3-methyl-1-tosyl-1H-indol-4-yl)-4-(3-methyl-4-((2-nitrophenyl)sulfonyl)piperazin-1-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CO[C@](C)(C(N)=O)C(F)(F)F)(NS(=O)(=O)c1ccccc1[N+](=O)[O-])c1cc(Br)ccc1F
Reaction #168760
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCCCN(CCN1CCS(=O)(=O)CC1)S(=O)(=O)c1ccccc1[N+](=O)[O-]
Reaction #172743
title compound
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OCCCNCCN1CCS(=O)(=O)CC1
Reaction #172744
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(SCCO)c([N+](=O)[O-])c1
Reaction #176779
DOI: 10.1039/C8SC04228D
COCC(NS(=O)(=O)c1ccccc1[N+](=O)[O-])C(=O)NC(Cc1ccc2ccccc2c1)C(=O)OC
Reaction #179666
DOI: 10.1039/C8SC04228D
NSc1ccc([N+](=O)[O-])cc1[N+](=O)[O-]
Reaction #190137
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc2c(C3CCCCC3)c(-c3ccc(F)cc3OCC(=O)NCCCCCN(C)S(=O)(=O)c3ccccc3[N+](=O)[O-])n(C)c2c1
Reaction #194710
DOI: 10.1039/C8SC04228D
CCOC(=O)CN(CCNS(=O)(=O)c1ccc(C(F)(F)F)cc1[N+](=O)[O-])C(=O)Cn1cc(C)c(=O)[nH]c1=O
Reaction #194971
DOI: 10.1039/C8SC04228D
الصفحة 1التالي