2013
DOI: 10.1007/s10870-013-0408-z
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Syntheses and Crystal Structures of 1,5-Dioxaspiro[5.5]undecane-2,4-dione Derivatives

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Cited by 9 publications
(5 citation statements)
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“…The double bond length C10-C8 (1.371(7) Å) in (1), (C7-C9) (1.366(2) Å) (2), is likewise in agreement with those described earlier reported (1.3454(2) Å, 1.336(2) Å) [15]. The double bond C10-N1 in (1) (1.308(7) Å), C7-N2 (2) (1.3248(18) Å) is typical C-N single bond.…”
Section: Spectroscopic Propertiessupporting
confidence: 91%
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“…The double bond length C10-C8 (1.371(7) Å) in (1), (C7-C9) (1.366(2) Å) (2), is likewise in agreement with those described earlier reported (1.3454(2) Å, 1.336(2) Å) [15]. The double bond C10-N1 in (1) (1.308(7) Å), C7-N2 (2) (1.3248(18) Å) is typical C-N single bond.…”
Section: Spectroscopic Propertiessupporting
confidence: 91%
“…The selected bond distances and bond angles of 1 and 2 are listed in Table 1 described earlier reported (1.3454(2) Å, 1.336(2) Å) [15]. The double bond C10-N1 in (1) (1.308(7) Å), C7-N2 (2) (1.3248(18) Å) is typical C-N single bond.…”
Section: Crystal Structuresmentioning
confidence: 79%
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“…The presence of oxaspirocyclic compounds in various natural products has also emerged, increasing interest due to their important biological activities, such as antimicrobial [9,10], antitumor [11] ,antiproliferative [12], antiviral [13], antiplasmodial [14] and antihistamic [15] activity etc. Based on these reasons, our group began to synthesize various oxaspirocyclic compounds and study their chemical properties [16][17][18][19]. In addition, to the best of our knowledge, oxaspirocyclic compounds derived from 6,10-dioxaspiro [4.5]decane-7,9-dione are very rare.…”
Section: Introductionmentioning
confidence: 99%