ORGANOTIN SUBSTITUTED CHOLESTERYL ETHERS AND ESTERS
Author:
Publisher
Walter de Gruyter GmbH
Subject
Materials Chemistry,Metals and Alloys,Condensed Matter Physics,General Chemistry
Link
https://www.degruyter.com/document/doi/10.1515/MGMC.1998.21.12.751/pdf
Reference34 articles.
1. In vitro effect of organotin-substituted steroids in human tumor cell lines
2. DI-n-BUTYL-, TRI-n-BUTYL- AND TRIPHENYLTIN STEROIDCARBOXYLATES: SYNTHESIS, NMR CHARACTERIZATION AND IN VITRO ANTITUMOUR ACTIVITY
3. Allylically Stannylated Cholestenes: The Synthesis of 3α-(Triphenylstannyl)cholest-4-ene, 7α-(Tributylstannyl)- and 7α-(Triphenylstannyl)cholest-5-en-3-one, and 7α-(Triphenylstannyl)-cholest-5-en-3β-ol
4. Intramolecular O.fwdarw.Sn coordination in (Z)-17-[2-(triphenylstannyl)vinyl]-4-estren-17-ol: evidence by x-ray diffraction analysis and iodo demetalation
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4. Hydroxy group interactions in stannylated carbohydrates. Structures and thermal stabilities of 5-deoxy-5-C-(Ph3Sn)-1,2-O-isopropylidene-α-D-xylofuranose, 5-deoxy-5-C-(IPh2Sn)-1,2-O-isopropylidene-α-D- and -L-xylofuranose, and 5-deoxy-5-C-(I2PhSn)-1,2-O-isopropylidene-α-D- and -L-xylofuranose;J. Chem. Soc., Perkin Trans. 1;2002
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