(1R,5R,6R,8R,9R,10R,11R,13R)-3-ALLYL-6,13-DIBUTYL-9,10-BIS-METHOXYMETHYL-8,11-DIMETHYL-2,4-DIOXA-3-BORA-TRICYCLO-[7.4.0.0(5,10)]-TRIDECANE
Compound with spectra: 1 NMR
![(1R,5R,6R,8R,9R,10R,11R,13R)-3-ALLYL-6,13-DIBUTYL-9,10-BIS-METHOXYMETHYL-8,11-DIMETHYL-2,4-DIOXA-3-BORA-TRICYCLO-[7.4.0.0(5,10)]-TRIDECANE](/api/compound/KEV8E8KmZ62.png?ph=true&h=300&w=458 "(1R,5R,6R,8R,9R,10R,11R,13R)-3-ALLYL-6,13-DIBUTYL-9,10-BIS-METHOXYMETHYL-8,11-DIMETHYL-2,4-DIOXA-3-BORA-TRICYCLO-[7.4.0.0(5,10)]-TRIDECANE")
| SpectraBase Compound ID | KEV8E8KmZ62 |
|---|---|
| InChI | InChI=1S/C26H47BO4/c1-7-10-12-21-16-20(5)26(18-29-6)24-22(13-11-8-2)15-19(4)25(26,17-28)23(21)30-27(31-24)14-9-3/h9,19-24,28H,3,7-8,10-18H2,1-2,4-6H3/t19?,20?,21?,22?,23-,24-,25+,26?/m1/s1 |
| InChIKey | YKJQXFLSXFYTCT-HVSQCNKISA-N |
| Mol Weight | 434.5 g/mol |
| Molecular Formula | C26H47BO4 |
| Exact Mass | 434.35674 g/mol |
| Enantiomer InChIKey | YKJQXFLSXFYTCT-GGJZFFHISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3-Formyl-4-furyl-2-hydroxy-2-methyl-5-nitro-6-phenylcyclohexanecarboxylic acid methyl ester
Aureolacetat
Methyl (4R,5S,7R,8R,9S)-8,9-Isopropylidenedioxy-2-benzyl-7-[(methoxymethoxy)methyl]-1,6-dioxa-2-azaspiro[4.4]nonane-4-carboxylate
1-Amino-3-[3-(2,4-dichlorobenzyl)oxyphenyl]pyrido[1,2-a]benzimidazole-2,4-dicarbonitrile
Methyl (4S,5S,7R,8R,9S)-8,9-Isopropylidenedioxy-2-benzyl-7-[(methoxymethoxy)methyl]-1,6-dioxa-2-azaspiro[4.4]nonane-4-carboxylate
Indeno[1,2-b]oxireno[c]pyridazin-9-ol, 9-ethyl-1a,2,3,9-tetrahydro-, (1a.alpha.,9.beta.,9aS*)-(.+-.)-
LESPECYRTIN_E_1
1,3,6-Methenocyclopenta[cd]pentalen-5(1H)-one, octahydro-7-phenyl-
3,6,11,14-TETRAMETHYL-17-(4-METHYLPHENYL)-17H-CYCLOPENTA-[1,2-L:3,4-L']-DIPHENANTHRENE
4,5-Dicarbomethoxy-2,7-epoxy-anti, syn-tetracyclo(6.2.2.1/3,6/.0/2,7/)dodeca-4,9-diene
| Title | Journal or Book | Year |
|---|---|---|
| Computer-Aided Design of Chiral Ligands. Part III. A Novel Ligand for Asymmetric Allylation Designed Using Computational Techniques | Organic Letters | 2002 |