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ANTI,ANTI-2,14-DIBROMO-8,20-METHANO-BIS-(6-H,12-H-5,11-METHANO-[B,F]-[1,5]-DIAZOCINE)-[2,1-B;8,7-F]-[1,5]-DIAZOCINE

Compound with spectra: 2 NMR

ANTI,ANTI-2,14-DIBROMO-8,20-METHANO-BIS-(6-H,12-H-5,11-METHANO-[B,F]-[1,5]-DIAZOCINE)-[2,1-B;8,7-F]-[1,5]-DIAZOCINE
SpectraBase Compound ID BYJYCmIUArI
InChI InChI=1S/C33H28Br2N6/c34-22-1-3-28-20(9-22)11-36-17-38(28)13-24-26-15-40-19-41(32(26)7-5-30(24)36)16-27-25-14-39-18-37(31(25)6-8-33(27)40)12-21-10-23(35)2-4-29(21)39/h1-10H,11-19H2
InChIKey QRCAVPGWSZBNPW-UHFFFAOYSA-N
Mol Weight 668.4 g/mol
Molecular Formula C33H28Br2N6
Exact Mass 666.074221 g/mol

View Spectrum of ANTI,ANTI-2,14-DIBROMO-8,20-METHANO-BIS-(6-H,12-H-5,11-METHANO-[B,F]-[1,5]-DIAZOCINE)-[2,1-B;8,7-F]-[1,5]-DIAZOCINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of ANTI,ANTI-2,14-DIBROMO-8,20-METHANO-BIS-(6-H,12-H-5,11-METHANO-[B,F]-[1,5]-DIAZOCINE)-[2,1-B;8,7-F]-[1,5]-DIAZOCINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • SYN,ANTI-2,14-DIBROMO-8,20-METHANO-BIS-(6-H,12-H-5,11-METHANO-[B,F]-[1,5]-DIAZOCINE)-[2,1-B;8,7-F]-[1,5]-DIAZOCINE
JJPUUEUDVFXUQJ-UHFFFAOYSA-N
FGOJAYGURUTNMI-UHFFFAOYSA-N
WLEBEMZLVXZJCC-UHFFFAOYSA-N
N-(2-chlorobenzyl)-3-(1-(mesitylmethyl)-2,4-dioxo-1,4-dihydro-3(2H)-quinazolinyl)propanamide
2,8-dimethyl-13-(2-furyl)-6H,12H-5,11-methanedibenzo[b,f][1,5]diazocine
N-(2-chlorobenzyl)-4-(1-(mesitylmethyl)-2,4-dioxo-1,4-dihydro-3(2H)-quinazolinyl)butanamide
2H-1,3-benzoxazine-2,4(3H)-dione, 6,8-dibromo-3-(2-ethylphenyl)-
N-(2-chlorobenzyl)-4-[(1-[2-(4-methoxyanilino)-2-oxoethyl]-2,4-dioxo-1,4-dihydro-3(2H)-quinazolinyl)methyl]benzamide
3',3''-Dimethyl-1,5-(endo)-{[(.alpha.-methoxycarbonyl)ethyl]methylene}-1,5-diaza-dibenzo[3,4-c : 7,8-c']cyclooctane
N-(2-chlorobenzyl)-4-[(1-[2-(dipropylamino)-2-oxoethyl]-2,4-dioxo-1,4-dihydro-3(2H)-quinazolinyl)methyl]benzamide
Title Journal or Book Year
A Desymmetrization Route to Fused Tröger's Base Analogues:  Synthesis, Isolation, and Characterization of the First Anti-Anti Diastereomer of a Fused Tris-Tröger's Base Analogue Organic Letters 2005
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