817-80-1Relevant academic research and scientific papers
PROCESS FOR THE MANUFACTURING OF A POLYMER WITH URETHANE GROUPS
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Page/Page column 27-28, (2019/03/05)
Object of the invention is a process for the manufacturing of a polymer with urethane groups, wherein in a first alternative A)a five-membered cyclic monothiocarbonate B)a compound with at least two amino groups, selected from primary or secondary amino groups, and C)a compound which at least two functional groups that react with a group -SH or, in case of a carbon-carbon triple bond as functional group that react with a group -SH, a compound with at least one carbon-carbon triple bond are reacted or wherein in a second alternative A)a five-membered cyclic monothiocarbonate and D)a compound with at least one primary or secondary amino group and at least one functional group that reacts with a group -SH.
PROCESS FOR THE MANUFACTURING OF A POLYMER WITH URETHANE GROUPS
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Page/Page column 31-33, (2019/03/05)
Process for the manufacturing of a polymer with urethane groups, wherein in a first alternative a compound A) with at least two five-membered cyclic monothiocarbonate groups and a compound B) with at least two amino groups, selected from primary or second
METHOD FOR THE PREPARATION OF THIOCARBONATES
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Page/Page column 21-22, (2019/03/05)
Process for the preparation of a compound with at least one five-membered cyclic monothiocar- bonate group wherein a) a compound with at least one epoxy group is used as starting material b) the compound is reacted with phosgene or an alkyl chloroformate
Imidazopyridine azolidinones
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, (2008/06/13)
PCT No. PCT/EP95/02954 Sec. 371 Date Jan. 28, 1997 Sec. 102(e) Date Jan. 28, 1997 PCT Filed Jul. 26, 1995 PCT Pub. No. WO96/03405 PCT Pub. Date Feb. 8, 1996Imidazopyridine-azolidinones are useful for treating or preventing amenable gastro-intestinal ailme
Reaction of Epoxides with Chlorocarbonylated Compounds Catalyzed by Hexaalkylguanidinium Chloride
Gros, P.,Perchec, P. Le,Senet, J. P.
, p. 4925 - 4930 (2007/10/02)
Silica-supported guanidinium chloride (PBGSiCl) exhibits efficient chemo- and regiospecific catalytic activity in the ring opening of epoxides with various electrophiles.This reaction allows the preparation of β-chloro esters and β-chloro chloroformates in high yield under neutral conditions which offer product stability and ease of product isolation.
