C07C209/62

CARBOHYDRATE CROSSLINKER

The invention relates to a hydrogel product comprising glycosaminoglycan molecules as the swellable polymer, wherein the glycosaminoglycan molecules are covalently crosslinked via crosslinks comprising a spacer group selected from the group consisting of di-, tri-, tetra-, and oligosaccharides.

METHOD OF PRODUCING THIOURETHANE RESIN RAW MATERIAL AND APPLICATION THEREOF, METHOD OF PRODUCING POLYTHIOL COMPOSITION AND APPLICATION THEREOF, AND POLYTHIOL COMPOSITION

A method of producing a thiourethane resin raw material, the method including comprising the step of generating the thiourethane resin raw material by reacting a thiourethane resin and an active hydrogen compound with each other.

METHOD OF PRODUCING THIOURETHANE RESIN RAW MATERIAL AND APPLICATION THEREOF, METHOD OF PRODUCING POLYTHIOL COMPOSITION AND APPLICATION THEREOF, AND POLYTHIOL COMPOSITION

A method of producing a thiourethane resin raw material, the method including comprising the step of generating the thiourethane resin raw material by reacting a thiourethane resin and an active hydrogen compound with each other.

PROCESS FOR PREPARING (R)-4-AMINOINDANE AND CORRESPONDING AMIDES

A process for preparing 1,1,3-trimethylindan-4-amine of formula (I), or a salt thereof, enriched in one of its two enantiomers, in particular the (R) enantiomer,

##STR00001##

including chirally separating an optionally substituted 2,2,4-trimethyl-1,2,3,4-tetrahydroquinoline of formula (III)

##STR00002##

A process may prepare one or more optically active amides of formula (II)

##STR00003##

starting from compounds of formula (I).

PROCESS FOR PREPARING (R)-4-AMINOINDANE AND CORRESPONDING AMIDES

A process for preparing 1,1,3-trimethylindan-4-amine of formula (I), or a salt thereof, enriched in one of its two enantiomers, in particular the (R) enantiomer,

##STR00001##

including chirally separating an optionally substituted 2,2,4-trimethyl-1,2,3,4-tetrahydroquinoline of formula (III)

##STR00002##

A process may prepare one or more optically active amides of formula (II)

##STR00003##

starting from compounds of formula (I).

PROCESS FOR PREPARING (R)-4-AMINOINDANE AND CORRESPONDING AMIDES

A process for preparing 1,1,3-trimethylindan-4-amine of formula (I), or a salt thereof, enriched in one of its two enantiomers, in particular the (R) enantiomer,

##STR00001##

including chirally separating an optionally substituted 2,2,4-trimethyl-1,2,3,4-tetrahydroquinoline of formula (III)

##STR00002##

A process may prepare one or more optically active amides of formula (II)

##STR00003##

starting from compounds of formula (I).

Carbohydrate crosslinker

The invention relates to a hydrogel product comprising glycosaminoglycan molecules as the swellable polymer, wherein the glycosaminoglycan molecules are covalently crosslinked via crosslinks comprising a spacer group selected from the group consisting of di-, tri-, tetra-, and oligosaccharides.

Carbohydrate crosslinker

The invention relates to a hydrogel product comprising glycosaminoglycan molecules as the swellable polymer, wherein the glycosaminoglycan molecules are covalently crosslinked via crosslinks comprising a spacer group selected from the group consisting of di-, tri-, tetra-, and oligosaccharides.

Method for deacetylation of biopolymers
11254792 · 2022-02-22 · ·

A method for at least partial deacetylation of a biopolymer comprising acetyl groups, including: a1) providing a biopolymer including acetyl groups; a2) reacting the biopolymer including acetyl groups with hydroxylamine (NH.sub.2OH) or a salt thereof at a temperature of 100° C. or less for 2-200 hours to form an at least partially deacetylated biopolymer; and a3) recovering the at least partially deacetylated biopolymer.

Method for deacetylation of biopolymers
11254792 · 2022-02-22 · ·

A method for at least partial deacetylation of a biopolymer comprising acetyl groups, including: a1) providing a biopolymer including acetyl groups; a2) reacting the biopolymer including acetyl groups with hydroxylamine (NH.sub.2OH) or a salt thereof at a temperature of 100° C. or less for 2-200 hours to form an at least partially deacetylated biopolymer; and a3) recovering the at least partially deacetylated biopolymer.