Deacylation reactions of 20-acetyl dinorcholanic lactones and 20,23-diacetyl furost-22-enes-Reference-Cited by-同舟云学术

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Deacylation reactions of 20-acetyl dinorcholanic lactones and 20,23-diacetyl furost-22-enes

Published:2010-03 Issue:3 Volume:75 Page:240-244
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Hernández-Linares Ma. Guadalupe,Sandoval-Ramírez Jesús,Meza-Reyes Socorro,Montiel-Smith Sara,Fernández-Herrera María A.,Bernès Sylvain

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

Reference21 articles.

1. Medicinal natural products. A biosynthetic approach;Dewick,2002

2. Steroid studies. VI. Studies on the constitution of sargasterol;Tsuda;J Am Chem Soc,1958

3. New sources of steroid sapogenins. XIX. 20S-Hydroxyvespertilin, a new steroid lactone from Solanum vespertilio;Gonzalez;Tetrahedron,1973

4. Sterols of scallop. Part II. Structure of unknown sterols by combination gas–liquid chromatography and mass spectrometry;Idler;Steroids,1976

5. Minor and trace sterols in marine invertebrate. Part 3. Novel marine sterols with modified bile acid side chain from the sea pen Ptilosarcus gurneyi;Vanderah;Tetrahedron Lett,1977

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1. A synthesis of cephalostatin 1;Tetrahedron;2019-03

2. The synthesis and antifungal activity of (20 S )-3β-acetoxy-5α-pregnane-20,16β-carbolactone against fluconazole – Resistant Candida cells;Steroids;2017-02

3. Total Synthesis of Linckosides A and B, the Representative Starfish Polyhydroxysteroid Glycosides with Neuritogenic Activities;Journal of the American Chemical Society;2015-12-01

4. Synthesis and biological evaluation of the glycoside (25R)-3β,16β-diacetoxy-22-oxocholest-5-en-26-yl β-d-glucopyranoside: A selective anticancer agent in cervicouterine cell lines;European Journal of Medicinal Chemistry;2011-09

5. Synthesis of the steroidal glycoside (25R)-3β,16β-diacetoxy-12,22-dioxo-5α-cholestan-26-yl β-d-glucopyranoside and its anti-cancer properties on cervicouterine HeLa, CaSki, and ViBo cells;European Journal of Medicinal Chemistry;2010-11

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