(3R)-1-[(20S)-20-(Dimethylamino)-4β-hydroxy-5α-pregnan-3β-yl]-3-isopropylazetidin-2-one Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

This alkaloid, in which the pregnane keto group of the preceding base is reduced to a secondary hydroxyl group, occurs in small amounts in Pachysandra termi_x0002_nalis Sieb. et Zucco It is laevorotatory having [O:]D - 18° (CHC13). Oxidation with chromic acid yields Pachystermine A.

Einzelnachweise

Kikuchi, Uyeo., Tetrahedron Lett., 3473 (1965)
Kikuchi, Uyeo., Chern. Pharrn. Bull., 15, 549 (1967)
Partial synthesis:
Kikuchi et aZ., Tetrahedron Lett., 909 (1968)

(3R)-1-[(20S)-20-(Dimethylamino)-4β-hydroxy-5α-pregnan-3β-yl]-3-isopropylazetidin-2-one Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

(3R)-1-[(20S)-20-(Dimethylamino)-4β-hydroxy-5α-pregnan-3β-yl]-3-isopropylazetidin-2-one Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate

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• Pachystermine B
• (3R)-1-[(20S)-20-(Dimethylamino)-4β-hydroxy-5α-pregnan-3β-yl]-3-isopropylazetidin-2-one
• 2-Azetidinone, 1-[(3β,4β,5α,20S)-20-(dimethylamino)-4-hydroxypregnan-3-yl]-3-(1-methylethyl)-, (3R)-
• 6157-00-2