ROHKJGMMGALLHR-UHFFFAOYSA-N
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 5VcZPdbjcuh |
|---|---|
| InChI | InChI=1S/C72H72N.F2H/c1-69(2,3)53-33-51(34-54(39-53)70(4,5)6)61-37-47-23-15-19-27-59(47)67-63(61)43-73(41-49-31-29-45-21-13-17-25-57(45)65(49)66-50(42-73)32-30-46-22-14-18-26-58(46)66)44-64-62(38-48-24-16-20-28-60(48)68(64)67)52-35-55(71(7,8)9)40-56(36-52)72(10,11)12;1-2/h13-40H,41-44H2,1-12H3;1H/q+1;-1 |
| InChIKey | ROHKJGMMGALLHR-UHFFFAOYSA-N |
| Mol Weight | 990.4 g/mol |
| Molecular Formula | C72H73F2N |
| Exact Mass | 989.571108 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
1-[2,6-DI-(NAPHTHALEN-2-YL)-3H-DINAPHTO-[2,1-C:1',2'-E]-AZEPIN-4-(5H)-YL]-3-(DIPHENYLPHOSPHINO)-PROPAN-1-ONE
(R)-6-[(1S)-1-Benzyl-2-oxo-2-(2-oxo-1,3-oxazolidin-3-yl)ethyl-4,9-dimethyl-3,4,5,6,7,8,9,10-octahydro-dinaphtho[2,1-f:1',2'-h][1,2,4,11]tetrazacyclododecine-5,8-dione
N'-[(E)-(2-methoxy-1-naphthyl)methylidene]-2-[(4-oxo-3-phenyl-3,4,5,6,7,8-hexahydro[1]benzothieno[2,3-d]pyrimidin-2-yl)sulfanyl]acetohydrazide
cis-5,6,6a,12c-Tetrahydrodibenzo[a,i]biphenylen-12c-ol
(S)-1-[2'-[[([2"-S-(2".alpha.,3a".alpha.,4".alpha.-7a".alpha.)]Octahydro-7",8",8"-trimethyl-4",7"-methanonenzofuran-2"-yl)oxy]methyl]-1'-naphthalenyl]isoquinoline
(R)-1-[2'-[[([2"-S-(2".alpha.,3a".alpha.,4".alpha.-7a".alpha.)]Octahydro-7",8",8"-trimethyl-4",7"-methanonenzofuran-2"-yl)oxy]methyl]-1'-naphthalenyl]isoquinoline
2-[(6,6-dimethyl-4-oxo-3-phenyl-3,5,6,8-tetrahydro-4H-pyrano[4',3':4,5]thieno[2,3-d]pyrimidin-2-yl)sulfanyl]-N-(2-methoxyphenyl)acetamide
3-cyano-3-(2-cyanoethyl)-4-methylene-2H-benzofuro[3,2-b]pyridine-1-carboxylic acid ethyl ester
1,4-Ethanonaphthalene-9,10-dione, 1,3-bis(1,1-dimethylethyl)-1,4-dihydro-
4,9-Diamino-5,7-dimethyl-2-p-tolyl-2H-pyrrolo[3,4-g]phthalazine-1,6,8-trione
| Title | Journal or Book | Year |
|---|---|---|
| Highly Enantioselective Michael Addition of Silyl Nitronates to α,β-Unsaturated Aldehydes Catalyzed by Designer Chiral Ammonium Bifluorides: Efficient Access to Optically Active γ-Nitro Aldehydes and Their Enol Silyl Ethers | Journal of the American Chemical Society | 2003 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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