بحث البنية الفرعية

131484

CCC#Cc1cccc[n+]1N.Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1
Reaction #9275
N-amino-2-(1-butynyl)pyridinium mesitylenesulfonate
المردود 39.1%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc2ccccn2n1
Reaction #9276
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(S(=O)(=O)Cl)cc1
Reaction #43888
white solid
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cccc(Oc2ccc(C(=O)C(=O)c3ccccc3)cc2)c1
Reaction #54306
4-(3-ethynylphenoxy)benzil
المردود 65.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cccc(Oc2ccc(C(=O)OC(=O)c3ccc(Oc4cccc(C#C)c4)c4ccccc34)c3ccccc23)c1
Reaction #55251
4-(3-ethynylphenoxy)naphthalic anhydride
المردود 80.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cccc(Oc2ccc(C(=O)OC(=O)c3ccc(Oc4cccc(C#C)c4)c4ccccc34)c3ccccc23)c1
Reaction #55252
4-(3-ethynylphenoxy)naphthalic anhydride
المردود 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn2ccccc2c1C(=O)c1ccc(Br)cc1
Reaction #65482
(4-bromophenyl) (2-butyl pyrazolo(1,5-a) pyridin-3-yl) methanone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn2c(C)cccc2c1C(=O)c1ccc(Br)cc1
Reaction #65493
(4-bromophenyl) (2-butyl 7-methyl pyrazolo(1,5-a) pyridin-3-yl) methanone
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1.N[n+]1ccc(Cl)cc1Cl
Reaction #72326
1-amino-2,4-dichloropyridinium 2,4,6-trimethylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
C[N+](C)(CCOC(=O)Oc1ccccc1)CCOC(=O)Oc1ccccc1.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #80267
5
DOI: 10.6084/m9.figshare.5104873.v1
C#C[C@@H](C)N(OC(=O)Oc1ccccc1)C(=O)Oc1ccccc1
Reaction #80471
(R)-N,O-bis(phenoxycarbonyl)-N-(3-butyn-2-yl)hydroxylamine
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ncccc1OCCCl
Reaction #83825
sulfonamide
المردود 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCn1cc[n+](CCCCc2ccc(NC(C)=O)cc2)c1.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #93524
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](C)/C=C/[C@@H](C)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #96101
ergosterol tosylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H](C)/C=C/[C@@H](C)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #96102
ergosterol tosylate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C[N+](C)(C)c2ccccc2)cc1
Reaction #255021
DOI: 10.1039/C8SC04228D
CNCCCCCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)F
Reaction #265172
DOI: 10.1039/C8SC04228D
CN(CCCCCOc1ccc(C2=C(c3ccccc3)CCCc3cc(OC4CCCCO4)ccc32)cc1)CCCC(F)(F)C(F)(F)F
Reaction #279251
DOI: 10.1039/C8SC04228D
Cc1cc(C)c(S(=O)(=O)[O-])c(C)c1.N[n+]1ccc(Cl)cc1Cl
Reaction #306550
1-amino-2,4-dichloropyridinium 2,4,6-trimethylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c([nH]1)-c1ccccc1N(C(=O)c1ccc(CNC(=O)C3CC3)c(C)c1)CC2
Reaction #308173
title compound
المردود 53.0%DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي