Substructure Search

3304

CCCN(CCC)CCC(P(=O)(OCC)OCC)P(=O)(OCC)OCC
Reaction #2065
title compound
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNCCC(P(=O)(O)O)P(=O)(O)O
Reaction #2069
Compound
Yield 109.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOP(=O)(OCC)C(CCCCNCc1ccccc1)P(=O)(OCC)OCC
Reaction #2071
title compound
Yield 45.8%DOI: 10.6084/m9.figshare.5104873.v1
c1cc2n(c1)Cc1ccsc1NC2
Reaction #3581
9,10-dihydro-4H-pyrrolo[1,2-a]thieno[2,3-e][1,4]diazepine
DOI: 10.6084/m9.figshare.5104873.v1
c1cc2n(c1)Cc1ccsc1NC2
Reaction #3638
desired product
DOI: 10.6084/m9.figshare.5104873.v1
c1cc2n(c1)Cc1sccc1NC2
Reaction #3643
4,10-Dihydro-5H-pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)NCCc1nncn1-2
Reaction #3653
desired product
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2c(c1)NCCc1cccn1-2
Reaction #3665
colorless oil
Yield 99.9%DOI: 10.6084/m9.figshare.5104873.v1
NCC(O)C1Cc2ccccc2N1C(=O)OCc1ccccc1
Reaction #6327
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C[S+](Cc2ccc(C)cc2)Cc2ccc(C)cc2)cc1.[F][Sb-]([F])([F])([F])([F])[F]
Reaction #6381
tris(p-methylbenzyl)sulfonium hexafluoroantimonate
Yield 87.3%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cccc(Cl)c1C[S+](Cc1c(Cl)cccc1Cl)Cc1c(Cl)cccc1Cl.[F][Sb-]([F])([F])([F])([F])[F]
Reaction #6383
tris(2,6-dichlorobenzyl)sulfonium hexafluoroantimonate
Yield 67.4%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C[S+](Cc2ccc(Cl)cc2)c2ccc(Cl)cc2)cc1.F[B-](F)(F)F
Reaction #6384
4-chlorophenylbis(4-chlorobenzyl)sulfonium tetrafluoroborate
Yield 77.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)CCN
Reaction #6913
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nn2c(OB(O)O)cccc2c1NC(=O)OC(C)(C)C
Reaction #9292
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)c1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12045
6-((1S)-1-hydroxy-ethyl)-(4R,9aR)-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)CC(O)c1ccc(NC(=O)c2ccccn2)cc1F
Reaction #41705
N-(4-(1,4-dihydroxy-3-methylbutyl)-3-fluorophenyl)pyridine-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)cc(CO)c1
Reaction #42399
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCNc2ccc(C(=O)OC)cc21
Reaction #42478
title compound
Yield 45.8%DOI: 10.6084/m9.figshare.5104873.v1
NC[C@@H]1CN(Cc2ccccc2)CC[C@@H]1O
Reaction #43618
(cis)-3-(aminomethyl)-1-(phenylmethyl)-4-piperidinol
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OC2CCSCC2)cc(C)c1B(O)O
Reaction #43904
title compound
Yield 71.0%DOI: 10.6084/m9.figshare.5104873.v1
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