Substructure Search

6593

O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #1036
4-bromo-3-chloro-3,4,4-trifiuorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(F)(Cl)C(F)(F)Cl
Reaction #1040
compound XI
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #61380
4-bromo-3,3,4,4-trifluorobutene
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1c[nH]c2ccc(F)c(Cl)c12
Reaction #85599
title compound
Yield 73.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)cnc1CCCCN
Reaction #255883
DOI: 10.1039/C8SC04228D
O=C(O)CC(F)(Cl)C(F)(F)Cl
Reaction #294910
DOI: 10.1039/C8SC04228D
[Ag]
Reaction #354353
silver
Yield 551.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)cnc1CCCCN
Reaction #401046
DOI: 10.1039/C8SC04228D
FC1OC(C(F)F)(C(F)(F)F)OC1(F)F
Reaction #415541
2-difluoromethyl-2-trifluoromethyl-4,4,5-trifluoro-1,3-dioxolane
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #526847
4-bromo-3-chloro-3,4,4-trifluorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(F)(Cl)C(F)(F)Cl
Reaction #526852
compound XI
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)cnc1CCCCN
Reaction #549682
4-(5-bromo-3-methyl-2-pyridyl)-butylamine
Yield 51.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)cnc1CCCCN
Reaction #549683
4-(5-bromo-3-methyl-2-pyridyl)-butylamine
Yield 46.1%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(F)C(F)(F)C(F)(F)OC(F)(F)C(F)(F)Br
Reaction #630705
FSO2CF2CF2OCF2CF2Br
DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O
Reaction #721759
Lactose
DOI: 10.6084/m9.figshare.5104873.v1
FC(Cl)C(F)(F)Sc1ccccc1
Reaction #753567
DOI: 10.1039/C8SC04228D
Cc1cc(Br)cnc1CCCCN
Reaction #760743
DOI: 10.1039/C8SC04228D
O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #813301
4-bromo-3-chloro-3,4,4-trifluorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(F)(Cl)C(F)(F)Cl
Reaction #813305
3,4-dichloro-3,4,4-trifluoro-butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CC(F)(Cl)C(F)(F)Cl
Reaction #813306
compound XI
DOI: 10.6084/m9.figshare.5104873.v1
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