2001
DOI: 10.1023/a:1014006806909
|View full text |Cite
|
Sign up to set email alerts
|

Untitled

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
13
0

Year Published

2002
2002
2015
2015

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 17 publications
(13 citation statements)
references
References 8 publications
0
13
0
Order By: Relevance
“…The protons at C-4 of the THP ring resonated just below 4.00 ppm except in cases where phenyl group is attached to N-3, while those bonded to C-2 were more de-shielded and resonated in the vicinity of 4.50 ppm. In the 13 C nmr spectra of the THPs, the most striking signal was due to carbonyl carbon (close to 190 ppm). Subsequently, the reaction of 3 with diamines and formaldehyde was examined.…”
Section: Resultsmentioning
confidence: 99%
See 2 more Smart Citations
“…The protons at C-4 of the THP ring resonated just below 4.00 ppm except in cases where phenyl group is attached to N-3, while those bonded to C-2 were more de-shielded and resonated in the vicinity of 4.50 ppm. In the 13 C nmr spectra of the THPs, the most striking signal was due to carbonyl carbon (close to 190 ppm). Subsequently, the reaction of 3 with diamines and formaldehyde was examined.…”
Section: Resultsmentioning
confidence: 99%
“…The IR spectra were recorded on a Perkin-Elmer 983 spectrometer. 1 H NMR and 13 C NMR spectra were recorded on Bruker ACF-300 spectrometer. The chemical shifts (δ ppm) and the coupling constants (Hz) are reported in the standard fashion with reference to TMS as internal reference.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…5 However, under these conditions dehydration proceeded to the end only for di-and trifluoromethyl substituted TK, whereas with the higher substituents γ-pyrones were obtained as by-products. …”
mentioning
confidence: 99%
“…In the present paper the cyclization of bis-polyfluoroalkyl-1,3,5-triketones 1c-e,h-j (or their cyclic hydrates 1a,b,f,g) 5 to form 2,6-bis-polyfluoroalkyl-4H-pyran-4-ones by the action of various dehydrating agents has been investigated, and the selection of the optimal conditions for the dehydration has been made.…”
mentioning
confidence: 99%