Busqueda de Subestructura

304367

CCCCCCCCCCCC1=NC(CC)(CO)CO1
Reaction #371252
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCC1=NC(C)CO1
Reaction #1173603
product
Rendimiento 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC1=NC(CC)CO1
Reaction #1173604
product
Rendimiento 89.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC1=NC(C)(C)CO1
Reaction #1173605
product
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC1=NC(C)(C)CO1
Reaction #1173607
product
Rendimiento 79.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC1=NC(C)(CO)CO1
Reaction #1173608
4-hydroxymethyl-4-methyl-2-undecyl-2-oxazoline
Rendimiento 84.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC1=NC(CC)(CO)CO1
Reaction #1173609
product
Rendimiento 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCC(C1=NC(C)(C)CO1)C(C)C
Reaction #1173612
disubstituted product
Rendimiento 14.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCC1=NC(CC)CO1
Reaction #1297951
DOI: 10.1039/C8SC04228D
CC[C@H](C)[C@H]1COC(CCC2OC(C)(C)N(C(=O)OC(C)(C)C)[C@H]2CC2CCCCC2)=N1
Reaction #1809448
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2cc(C=O)cc(OCc3ccccc3)c2C1
Reaction #2088460
DOI: 10.1038/s41557
COc1ccc(CNC(C)c2cnccn2)cc1
Reaction #2093356
DOI: 10.1038/s41557
C[C@@H]1CC=C(O[Si](C)(C)C(C)(C)C)CC1
Reaction #2093502
DOI: 10.1038/s41557
CC(c1ccccc1)c1cc(Cl)nnc1N
Reaction #2093705
DOI: 10.1038/s41557
O=C(O)CC(c1ccccc1)C(F)(F)F
Reaction #2094193
DOI: 10.1038/s41557
O=C(O)CC(c1ccccc1)C(F)(F)F
Reaction #2094231
DOI: 10.1038/s41557
CC(c1ccccc1)c1cc(Cl)nnc1N
Reaction #2094909
DOI: 10.1038/s41557
CC1C(=O)CC1c1ccccc1
Reaction #2095356
DOI: 10.1038/s41557
CC1C(=O)CC1c1ccccc1
Reaction #2095492
DOI: 10.1038/s41557
CC1CNC(=O)c2ccccc21
Reaction #2095668
DOI: 10.1038/s41557
Página 1Siguiente