1999
DOI: 10.1002/(sici)1098-1071(1999)10:6<475::aid-hc7>3.0.co;2-s
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Synthesis and quantitative structure-activity relationship of a new series of chiral 4-alkoxycarbonyl-2-(alkylamino)-1,3,2-oxa or thiazaphospholidine-2-ones

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Cited by 6 publications
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“…In the literature it has been reported that reaction of L-cysteine ethyl ester hydrochloride with carbon disulfide in the presence of triethyl amine in CH 2 Cl 2 at room temperature yielded a five membered ring [14]. Similarly, esterification of L-(R)-cysteine followed by reaction with phosphoryl chloride and two moles of triethylamine, yielded cyclic phosphoramidothiolic chloride [15], a five membered ring.…”
Section: Introductionmentioning
confidence: 99%
“…In the literature it has been reported that reaction of L-cysteine ethyl ester hydrochloride with carbon disulfide in the presence of triethyl amine in CH 2 Cl 2 at room temperature yielded a five membered ring [14]. Similarly, esterification of L-(R)-cysteine followed by reaction with phosphoryl chloride and two moles of triethylamine, yielded cyclic phosphoramidothiolic chloride [15], a five membered ring.…”
Section: Introductionmentioning
confidence: 99%