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6464

[N-]=[N+]=CC(=O)COc1ccccc1Oc1cc(Oc2ccc(Cl)cc2Cl)ccc1[N+](=O)[O-]
Reaction #49802
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)C=[N+]=[N-]
Reaction #64789
(S)-3-[[[(1,1-Dimethylethyl)oxy]carbonyl]amino]-2-oxo-1-diazo-4-phenylbutane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)C(=O)C=[N+]=[N-]
Reaction #64809
(S)-3-[[[(1,1-Dimethylethyl)oxy]carbonyl]amino]-2-oxo-1-diazo-4-phenylbutane
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)[C@H](C)[C@H]12
Reaction #65560
4-nitrobenzyl (4R, 5R, 6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3, 7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)[C@H](C)[C@@H]12
Reaction #65563
4-nitrobenzyl (4R, 5S, 6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3, 7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](n2ccc(=O)[nH]c2=O)C(=O)C1=[N+]=[N-]
Reaction #65678
title compound
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=C(c1ccccc1)c1ccc(CO)cc1
Reaction #68729
5
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOCc1ccc(C(=[N+]=[N-])c2ccccc2)cc1
Reaction #68732
11
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCC(C1CCCC1)n1cc(-c2ncnc3c2ccn3COCC[Si](C)(C)C)cn1
Reaction #69285
4-[1-(1-Cyclopentylbut-3-yn-1-yl)-1H-pyrazol-4-yl]-7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
C#CCC(C1CCCC1)n1cc(-c2ncnc3c2ccn3COCC[Si](C)(C)C)cn1
Reaction #73316
4-[1-(1-Cyclopentylbut-3-yn-1-yl)-1H-pyrazol-4-yl]-7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@H]1C(=O)C=[N+]=[N-]
Reaction #73863
title compound
Выход 69.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC1CCC(S(=O)(=O)C(=[N+]=[N-])S(=O)(=O)C2CCC(CCCCC)CC2)CC1
Reaction #79465
bis(4-n-pentylcyclohexylsulfonyl)diazomethane
Выход 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1CCC(S(=O)(=O)C(=[N+]=[N-])S(=O)(=O)C2CCC(CCCC)CC2)CC1
Reaction #79467
bis(4-n-butylcyclohexylsulfonyl)diazomethane
Выход 20.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)Oc1ccc(C[C@H](NC(=O)OCc2ccccc2)C(=O)C=[N+]=[N-])cc1
Reaction #82351
benzyl [2-(4-tert.butoxyphenyl)-1(S)-(2-diazoacetyl)ethyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
C#C[C@H](C)NC(=O)OC(C)(C)C
Reaction #85686
(S)-tert-butyl but-3-yn-2-ylcarbamate
Выход 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(C)(C)C)cc(C)c1C1C(=O)CC(C)(C)CC1=O
Reaction #93556
2-(2',6'-dimethyl-4'-t-butylphenyl)-5,5-dimethyl-1,3-cyclohexanedione
Выход 11.0%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=CC(=O)c1ccc(Br)c2ccccc12
Reaction #159003
1-(4-bromonaphthalen-1-yl)-2-diazoethanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CBr)c1ccc(Br)c2ccccc12
Reaction #159004
2-bromo-1-(4-bromo-naphthalen-1-yl)-ethanone
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1cnc(C2CCCN2C(=O)OC(C)(C)C)n1COCC[Si](C)(C)C
Reaction #159024
2-[5-Ethynyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc(OC(C)C)cn1
Reaction #163306
2-Ethynyl-5-isopropoxypyridine
DOI: 10.6084/m9.figshare.5104873.v1
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