Conversion of thioacetals to alkanes using Raney Nickel
Description: Thioacetals can be desulfurized to give alkanes through the use of Raney nickel (“Ra-Ni”) The rest of this page is available to MOC Members only. To get access to…
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Success Stories: How Corina Got The The “Hard” Professor – And Got An A+ Anyway
Does your school have that one “hard” organic chemistry instructor that most students try to avoid? Today’s success story comes from Corina, a student in Texas who got assigned the…
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Read moreNewman Projection of Butane (and Gauche Conformation)
…-30° to -150°). So there are four possibilities; syn-periplanar, anti-periplanar, syn-clinal (+ and -) and anti-clinal (+ and -). We generally don’t discuss clinal in introductory organic chemistry (since it…
Read moreStaggered vs Eclipsed Conformations of Ethane
…strain” is an analogy to the twisting force one experiences when you twist a spring or (more commonly) a rubber band – for instance, in a rubber-band driven propeller plane….
Read moreA Gallery of Some Interesting Molecules From Nature
…of pheromone traps as a popular alternative to pesticides. The molecule below is (Z)-9-tricosene, the pheromone that female houseflies release to attract males. This chemical, commercially known as Muscalure, is…
Read more350 Examples of Classic Org 1/Org 2 Reactions From “Organic Syntheses”
…Flickr: https://www.flickr.com/photos/182129490@N06/collections The set of 350 .CDX files can be downloaded here for free, along with an XLS that contains the DOIs. Coll Org Syn Chemdraw (.zip) including XLSX spreadsheet…
Read moreReaction Maps Now Available
…strain with the compressed version, so it’s been designed in a 4-quadrant format allowing it to be expanded 200% without any pages cutting off. (A 60-page non-compressed version is also…
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…CP-225,917 . Tetrahedron 2010 66 (1), 368-378. doi: 10.1016/j.tet.2009.10.071 Kim, J.; Ashenhurst, J. A.; Movassaghi, M. ; Total Synthesis of (+)-11,11′-Dideoxyverticillin A. Science 2009 324 (5924), 238-241 doi: 10.1126/science.1170777 Movassaghi,…
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