2003
DOI: 10.1002/chin.200308168
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and Antimicrobial Activity of Novel 2‐Alkyl/Arylcarbamato‐6‐ (1,1‐dimethylethyl) ‐3‐cyclohexyl‐3,4‐dihydro‐2H‐1,3,2‐benzoxazaphosphorine‐2‐oxides.

Abstract: Organo-phosphorus compoundsOrgano-phosphorus compounds S 0080 Synthesis and Antimicrobial Activity of Novel 2-Alkyl/Arylcarbamato-6-(1,1-dimethylethyl)-3-cyclohexyl-3,4-dihydro-2H-1,3,2-benzoxazaphosphorine-2-ox-ides. -Some of the compounds presented show significant antibacterial and antifungal activity. -(BABU, Y. H.; REDDY, P. V. G.; REDDY*, C. S.; REDDY, C. D.; DEVI*, P. U. M.; J.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2007
2007
2018
2018

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 3 publications
0
2
0
Order By: Relevance
“…Compounds 2a-2e and 2a 0 -2e 0 were prepared via an intermediary step that involved -(3-chloro-4-fluoroanilino)-2-cresol [13], 2-(cyclohexylaminomethyl)-4-tert-butylphenol [14] and 5,5 0 -dichloro-2,2 0 -dihydroxydiphenyl sulfide [15], 2,2 0 -dihydroxy (1,1 0 -binaphthol) [12], and their corresponding cyclic phosphorochloridates (1a-1e) and cyclic phosphorothiochloridates (1a 0 -1e 0 ). These intermediary compounds were prepared according to the procedures reported by Kiran et al [16] and Kasthuraiah et al [17].…”
Section: Synthetic Proceduresmentioning
confidence: 99%
“…Compounds 2a-2e and 2a 0 -2e 0 were prepared via an intermediary step that involved -(3-chloro-4-fluoroanilino)-2-cresol [13], 2-(cyclohexylaminomethyl)-4-tert-butylphenol [14] and 5,5 0 -dichloro-2,2 0 -dihydroxydiphenyl sulfide [15], 2,2 0 -dihydroxy (1,1 0 -binaphthol) [12], and their corresponding cyclic phosphorochloridates (1a-1e) and cyclic phosphorothiochloridates (1a 0 -1e 0 ). These intermediary compounds were prepared according to the procedures reported by Kiran et al [16] and Kasthuraiah et al [17].…”
Section: Synthetic Proceduresmentioning
confidence: 99%
“…According the results, the cyclohexyl and 3'nitrophenyl groups we encoded in 3a and 3b were found to have higher antitumor and antimicrobial activity. It has been shown in the literature [35][36][37][38] that cyclohexyl and nitrophenyl groups in the structure of the compounds show an effective antitumor and antimicrobial effect. Other compounds (3c-e) have shown modarate effect on the microorganisms.…”
Section: Resultsmentioning
confidence: 99%