Detail of "10430-90-7"

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Solid-phase synthesis of 2-amino-5-sulfanylthiazoles: Solid-phase synthesis of 2-amino-5-sulfanylthiazoles. Grimstrup, Marie; Zaragoza, Florencio (MedChem Research, Novo Nordisk A/S, Malov 2760, Den.). European Journal of Organic Chemistry, (17), 2953-2960 (English) 2002 Wiley-VCH Verlag GmbH & Co. KGaA.Some chemicals with cas registry numbers like 10430-90-7 are also used. CODEN: EJOCFK. ISSN: 1434-193X. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) A solid-phase synthesis that provides easy access to 2-amino-5-sulfanylthiazoles with variable substituents at C-2, C-4, and C-5 has been developed. The key step of this synthesis is a new C-sulfanylation of resin-bound 2-aminothiazoles by mixts. 10430-90-7 are also occured in this study. of various sulfur-contg. building blocks and iodine. The resulting 2-amino-5-sulfanylthiazoles were obtained in high purities and yields after cleavage from the support. This synthesis could also be conducted as a multicomponent reaction, in which treatment of resin-bound thioureas with mixts. of aryl bromomethyl ketones and sulfanylating reagents yielded 2-amino-5-sulfanylthiazoles directly. ..

Solid-phase synthesis of 2-amino-5-sulfanylthiazoles: Solid-phase synthesis of 2-amino-5-sulfanylthiazoles. Grimstrup, Marie; Zaragoza, Florencio (MedChem Research, Novo Nordisk A/S, Malov 2760, Den.). European Journal of Organic Chemistry, (17), 2953-2960 (English) 2002 Wiley-VCH Verlag GmbH & Co. KGaA.Some chemicals with cas registry numbers like 10430-90-7 are also used. CODEN: EJOCFK. ISSN: 1434-193X. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) A solid-phase synthesis that provides easy access to 2-amino-5-sulfanylthiazoles with variable substituents at C-2, C-4, and C-5 has been developed. The key step of this synthesis is a new C-sulfanylation of resin-bound 2-aminothiazoles by mixts. 10430-90-7 are also occured in this study. of various sulfur-contg. building blocks and iodine. The resulting 2-amino-5-sulfanylthiazoles were obtained in high purities and yields after cleavage from the support. This synthesis could also be conducted as a multicomponent reaction, in which treatment of resin-bound thioureas with mixts. of aryl bromomethyl ketones and sulfanylating reagents yielded 2-amino-5-sulfanylthiazoles directly. ..