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A Streamlined Synthesis of Androstadiene C-17 Ester Derivatives
Author(s) -
Fabrice Gallou,
Manuela SeegerWeibel,
Daniel Lupp
Publication year - 2011
Publication title -
chimia international journal for chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.387
H-Index - 55
eISSN - 2673-2424
pISSN - 0009-4293
DOI - 10.2533/chimia.2011.877
Subject(s) - yield (engineering) , solvent , derivative (finance) , chemistry , combinatorial chemistry , organic chemistry , biochemical engineering , materials science , engineering , business , finance , metallurgy
The development of a fully telescoped synthesis of a derivative of androstadiene C-17 esters made from epoxyparamethasone was demonstrated. This streamlining allowed for the elimination of isolation and solvent change after each synthetic step. Thus it not only drastically reduced the solvent waste, but also minimized the potential exposure to highly active intermediates thereby increasing the overall yield. The intuitively obvious advantage inherent to lowering the number of solvents was illustrated by applying standard green metrics.

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