Recherche de Sous-structure

446602

CCCCCCCCOC(=O)F
Reaction #93267
n-octyl fluoroformate
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCl)OCC1CCCO1
Reaction #174024
DOI: 10.1039/C8SC04228D
CC(OC(=O)CCOc1ccccc1N(C)C(=O)c1ccc(Cl)c(-c2cnc(C(F)(F)F)cc2C#N)c1)OC(=O)OC1CCCCC1
Reaction #174967
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(CCOC(=O)OCCl)CC1
Reaction #207639
DOI: 10.1039/C8SC04228D
CC1(OC(=O)OCI)CCCCC1
Reaction #208118
DOI: 10.1039/C8SC04228D
COc1cc(OCCO)c(F)c(C(Nc2ccc(C(N)=NC(=O)c3ccccc3)cc2)c2nc(OC(C)OC(=O)OC3CCCCC3F)n(-c3ncccn3)n2)c1
Reaction #222471
DOI: 10.1039/C8SC04228D
CCCCCCOC(=O)OC(C)OC(=O)c1c(I)c(NC(C)=O)c(I)c(N(C)C(C)=O)c1I
Reaction #226993
DOI: 10.1039/C8SC04228D
CC(Cl)OC(=O)OC1CCCCC1
Reaction #228508
DOI: 10.1039/C8SC04228D
CC(Cl)OC(=O)OCCCCC(CO[N+](=O)[O-])O[N+](=O)[O-]
Reaction #237039
DOI: 10.1039/C8SC04228D
CCCCOC(=O)OCCl
Reaction #251303
DOI: 10.1039/C8SC04228D
CC(OC(=O)OC1CCCCC1)OC(=O)c1ccc(-c2ccccc2C(C)OCC(O)CNC(C)(C)Cc2ccc3ccccc3c2)cc1
Reaction #253290
DOI: 10.1039/C8SC04228D
CCCCc1nc(Cl)c(C(=O)OC(C)OC(=O)OCCCC(O[N+](=O)[O-])C(C)O[N+](=O)[O-])n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #271527
DOI: 10.1039/C8SC04228D
CCCCCCCCOC(=O)OCCl
Reaction #280383
DOI: 10.1039/C8SC04228D
CCCCCCCCOC(=O)F
Reaction #283615
DOI: 10.1039/C8SC04228D
O=C(OCI)OCC1CCCO1
Reaction #287270
DOI: 10.1039/C8SC04228D
C=CC(=O)OCCCCOC(=O)OC(C)Cl
Reaction #300175
DOI: 10.1039/C8SC04228D
CC(Cl)OC(=O)OCCC(C)C(O[N+](=O)[O-])C(C)O[N+](=O)[O-]
Reaction #301649
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N[C@@H](CC(=O)N1CCn2c(C(F)(F)F)nc(C(=O)OCCOC(=O)OC3CCCCC3)c2C1)Cc1cc(F)c(F)cc1F
Reaction #308686
(R)-7-[3-tert-butoxycarbonylamino-4-(2,4,5-trifluoro-phenyl)-butyryl]-3-trifluoromethyl-5,6,7,8-tetrahydro-imidazo[1,5-a]pyrazine-1-carboxylic acid (1-cyclohexyloxycarbonyloxy)-ethyl ester
Rendement 69.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(Cl)c(C(=O)O[C@H](C)OC(=O)O[C@H]2CO[C@H]3[C@@H]2OC[C@H]3O[N+](=O)[O-])n1Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1
Reaction #309712
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(OCCOC(=O)c1cccc2c1CC(=CCCN1CCC(O)(c3ccc(Cl)cc3)CC1)c1cccnc1O2)OC1CCCCC1
Reaction #329723
titled compound
Rendement 116.7%DOI: 10.6084/m9.figshare.5104873.v1
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