Literature DB >> 18166206

Synthesis of novel steroidal D-ring substituted isoxazoline derivatives of 17-oxoandrostanes.

Abid H Banday1, Swarn Singh, M Sarwar Alam, Doma M Reddy, B D Gupta, H M Sampath Kumar.   

Abstract

A facile synthesis of isoxazoline derivatives of 17-oxoandrostane at the side chain of D-ring is reported. The scheme involves the transformation of the starting dehydroepiandrosterone acetate (ketone) to the Knoevenegel product, reduction to the nitrile, and elimination to the carboxaldehyde. Cycloaddition of nitrileoxides across olefinic aldehyde intermediate led to the synthesis of novel side chain isoxazoline derivatives.

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Year:  2007        PMID: 18166206     DOI: 10.1016/j.steroids.2007.10.014

Source DB:  PubMed          Journal:  Steroids        ISSN: 0039-128X            Impact factor:   2.668


  2 in total

1.  (20S,2''S)-20-[4'-(3''-Hydroxy-2''-methyl-prop-yl)-3'-methylisoxazol-5-yl]-5β-preg-nan-3β,16β-diol.

Authors:  María-Guadalupe Hernández Linares; Jesús Sandoval Ramírez; Socorro Meza Reyes; Sara Montiel Smith; Sylvain Bernès
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-11-28

2.  Synthesis and In vitro cytotoxic activity evaluation of (E)-16-(substituted benzylidene) derivatives of dehydroepiandrosterone.

Authors:  Mohsen Vosooghi; Hoda Yahyavi; Kouros Divsalar; Hashem Shamsa; Asma Kheirollahi; Maliheh Safavi; Sussan Kabudanian Ardestani; Sareh Sadeghi-Neshat; Negar Mohammadhosseini; Najmeh Edraki; Mehdi Khoshneviszadeh; Abbas Shafiee; Alireza Foroumadi
Journal:  Daru       Date:  2013-05-01       Impact factor: 3.117

  2 in total

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