Chemotherapy of hookworm infections

Sharma, Satyavan; Charles, Elizabeth S.

doi:10.1007/978-3-0348-7111-2_1

Cited by 2 publications

(7 citation statements)

References 133 publications

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“…In this case, the cyclization took place only to the nitrogen at position 3 in the pyrimidine system. Similarly, ethyl 5-oxo-2,3,6,9-tetrahydro-5H-pyrido [4 ,3 :4,5]thieno [2,3-d] [1,3]thiazolo[3,2-a]pyrimidine-8(7H)-carboxylate 10 was obtained from the reaction of 2 with aminoethanethiol hydrochloride in pyridine (Scheme 1).…”

Section: Resultsmentioning

confidence: 99%

“…• C. IR: ν = 3400, 3300, 3200, 3000, 2850, 1700, 1680, and 1600 cm [4 ,3 :4,5]thieno [3,2-e] [1,2,3,4…”

Section: Ethyl 3-amino-2-methyl-10-oxo-38910-tetrahydropyrido[4 3mentioning

confidence: 99%

“…• C. IR : ν = 3200-3300, 3000, 2900, 1700, 1680, and 1620 cm Ethyl 2-Hydrazino-10-oxo-8,9-dihydro-10H-pyrido [4 ,3 :4,5]thieno [2,3-d]- [1,3,4]…”

Section: -Thiadiazolo[32-a]-pyrimidine-7(6h)-carboxylate (12)mentioning

confidence: 99%

“…• C. IR: ν = 3100, 2990, 2940, 1750, 1710, 1680, and 1640 cm Ethyl 5-Oxo-2,3,6,9-tetrahydro-5H-pyrido [4 ,3 : 4,5]thieno [2,3-d] [1,3]…”

Section: D]pyrimidine-8(5h)-carboxylate (9)mentioning

confidence: 99%

“…The antiparasitic properties exhibited by a variety of isothiocyanates have been very well documented [1]. Furthermore, various substituted thioureas also have been reported to possess broad-spectrum anthelmintic activity [2].…”

Section: Introductionmentioning

confidence: 99%

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