DIAD

O=[N+]([O-])c1ccc(OCc2cccc(F)c2)c(Br)c1
Reaction #6912
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc(-c2nn3c(c2-c2ccnc4cc(OCc5ccncc5)ccc24)CCC3)nc1
Reaction #8378
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN1CC[C@@H](Oc2cc(N)ccc2Cl)C1
Reaction #8727
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN1CCN(c2c(C(=O)C(C)(C)C)oc3nc(-c4ccccc4Cl)c(-c4ccc(Cl)cc4)cc23)C(=O)C1=O
Reaction #8903
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N1Cc2cc3c(cc2C[C@H]1C(=O)O)NC(=O)C(c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1)O3
Reaction #41848
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)[C@H](Cc1ccc2c(c1)NC(=O)[C@H](c1ccc(OCc3ccc(Cl)c(Cl)c3)cc1)O2)NC(=O)OC(C)(C)C
Reaction #41850
(S)-2-tert-Butoxycarbonylamino-3-{(S)-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl}-propionic acid methyl ester
Ausbeute 56.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)[C@H](Cc1ccc2c(c1)N(C)C(=O)[C@H](c1ccc(OCc3ccc(Cl)c(Cl)c3)cc1)O2)NC(=O)OC(C)(C)C
Reaction #41851
(S)-2-tert-Butoxycarbonylamino-3-{(S)-2-[4-(3,4-dichloro-benzyloxy)-phenyl]-4-methyl-3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl}-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(S(=O)(=O)OCC2Cc3c(Cl)cc4c(c3O2)CCC4)cc1
Reaction #42227
(±)-(4-chloro-3,6,7,8-tetrahydro-2H-indeno[4,5-b]furan-2-yl)methyl 4-methylbenzenesulfonate
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
[N-]=[N+]=NCC1Cc2cc(Cl)c3ccccc3c2O1
Reaction #42248
(±)-(5-chloro-2,3-dihydronaphtho[1,2-b]furan-2-yl)methyl azide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(COc2cnc(COC(C)=O)cc2OCc2ccccc2)cc1
Reaction #43435
oil
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1cc2c(n[nH]1)OCC2
Reaction #43456
product
Ausbeute 16.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(Nc2ccc(Br)cc2F)c(-c2nnnn2CCC#N)cn(C)c1=O
Reaction #44201
desired product
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@H](Oc1ccc(Cl)cc1B(O)O)C(=O)O
Reaction #44376
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C[C@@H](OC(=O)c1ccc([N+](=O)[O-])cc1)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44633
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCOC(=O)N(Cc1ccc(OC)cc1)S(=O)(=O)NCC(=O)OCC
Reaction #45245
ethyl 2-((N-(butyloxycarbonyl)-N-(p-methoxybenzyl)sulfamoyl)amino)acetate
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCOC(=O)N(C)S(=O)(=O)NCC(=O)OCC
Reaction #45253
ethyl 2-((N-(butyloxycarbonyl)-N-methylsulfamoyl)amino)acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCN3CCOCC3)cc2C1=O
Reaction #46156
title compound
Ausbeute 128.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(O[C@@H](C)CO[Si](C)(C)C(C)(C)C)c1
Reaction #48767
title compound
Ausbeute 87.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC[C@H](C)Oc1cc(OCc2ccccc2)cc(C(=O)OC)c1
Reaction #48778
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1cc(OCc2ccccc2)cc(O[C@@H](C)CO[Si](C)(C)C(C)(C)C)c1
Reaction #48785
title compound
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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