Weight | 112.176 g/mol |
---|---|
Formula | C6H12N2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
1,4-diazabicyclo[3.2.1]octane (5167-08-8)
Alternate Names
- 5167-08-8
- 1,4-diazabicyclo[3.2.1]octane
-
SMILESC1CN2CCNC1C2
-
InChIKeyKYCAEEFYFFBAAP-UHFFFAOYSA-N
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Most-cited Publications
- Quantification of singlet oxygen generated by thermolysis of 3,3'-(1,4-naphthylene)dipropionate endoperoxide. Monomol and dimol photoemission and the effects of 1,4-diazabicyclo[2.2.2]octane (Journal of the American Chemical Society, 1989)
- Synthesis of chiral 2,3-disubstituted 1,4-diazabicyclo [2.2.2] octane. New ligand for the osmium-catalyzed asymmetric dihydroxylation of olefins (Tetrahedron Letters, 1992)
- Synthesis of substituted chromenes through the DABCO-catalyzed reaction of but-3-yn-2-one and methyl propiolate with salicyl N-tosylimines (DABCO = 1,4-diazabicyclo[2.2.2]octane). (Chemistry: A European Journal, 2006)
- 1,3-Dipolar cycloaddition reactions of imines of -amino-acid esters: X-ray crystal and molecular structure of methyl 4-(2-furyl)-2,7-diphenyl-6,8-dioxo-3,7-diazabicyclo[3.3.0]octane-2-carboxylate (Journal of The Chemical Society, Chemical Communications, 1978)
- Synthesis and antiproliferative properties of N3/8-disubstituted 3,8-diazabicyclo[3.2.1]octane analogues of 3,8-bis[2-(3,4,5-trimethoxyphenyl)pyridin-4-yl]methyl-piperazine. (European Journal of Medicinal Chemistry, 2007)
- Self-assembly of cage structures. Paper 12: The synthesis and crystal structures of 2,5-diazabicyclo[2.2.2]octane-3,6-dione-1,4-dicarboxylic acids and their diesters (Tetrahedron, 2002)
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