(6R,9R)-9-TERT.-BUTYL-3-ETHOXYCARBONYL-6-METHOXYCARBONYL-2,5-DIOXO-1-AZA-8-OXABICYClO-[3.3.0]-NONANE
Compound with spectra: 1 NMR
![(6R,9R)-9-TERT.-BUTYL-3-ETHOXYCARBONYL-6-METHOXYCARBONYL-2,5-DIOXO-1-AZA-8-OXABICYClO-[3.3.0]-NONANE](/api/compound/B9si5qpG5Nz.png?ph=true&h=300&w=458 "(6R,9R)-9-TERT.-BUTYL-3-ETHOXYCARBONYL-6-METHOXYCARBONYL-2,5-DIOXO-1-AZA-8-OXABICYClO-[3.3.0]-NONANE")
| SpectraBase Compound ID | B9si5qpG5Nz |
|---|---|
| InChI | InChI=1S/C16H23NO7/c1-6-23-12(20)9-7-10(18)16(14(21)22-5)8-24-13(15(2,3)4)17(16)11(9)19/h9,13H,6-8H2,1-5H3/t9?,13-,16-/m1/s1 |
| InChIKey | COEURVGANINDTG-FVYDNSIJSA-N |
| Mol Weight | 341.36 g/mol |
| Molecular Formula | C16H23NO7 |
| Exact Mass | 341.147452 g/mol |
| Enantiomer InChIKey | COEURVGANINDTG-LCQZPTMYSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3S,6R,7aR)-3-tert-Butyl-1,6,7,7a-tetrahydro-6-methyl-5-oxopyrrolo[1,2-c]oxazolidine-6,7a-dicarboxylic acid 7a-methyl ester
isopropyl 4-(2,3-dichlorophenyl)-2-methyl-5-oxo-1,4,5,6,7,8-hexahydro-3-quinolinecarboxylate
10-ACETYL-7-BENZYLOXY-4,12,13-TRIOXA-10-AZATETRACYCLO[7,3,1(3,6).0(2,8)]TRIDECAN-11-ONE
DULCISXANTHONE_B;1,6,7-TRIHYDROXY-3-METHOXY-2,8-BIS-(3-METHYL-2-BUTENYL)-XANTHONE
4-(2-Chloro-5-nitro-phenyl)-5-keto-2-methyl-4,6,7,8-tetrahydro-1H-quinoline-3-carboxylic acid methyl ester
3-ALPHA-ACETOXYMETHYL-3-BETA-HYDROXY-1-OXACEPHAM-BENZHYDRYLESTER
pyrano[2,3-c]pyrazole-5-carbonitrile, 6-amino-1,4-dihydro-4-(1-methyl-1H-pyrrol-2-yl)-3-phenyl-
(3R,3aR,9bS)-8-Bromo-1-methyl-3-phenyl-1,3,3a,9b-tetrahydro-2,5-dioxa-4-thia-1-aza-cyclopenta[a]naphthalene 4,4-dioxide
6-Diazo-7-(3,4,5-trimethoxyphenyl)-5H-indeno[5,6-d]-1,3-dioxol-5-one
8.alpha.,13-Epoxylabdane-2,20-diyl Chlorophosphate
| Title | Journal or Book | Year |
|---|---|---|
| Regioselective Dieckmann cyclisations leading to enantiopure highly functionalised tetramic acid derivatives | Journal of the Chemical Society, Perkin Transactions 1 | 1998 |