Uploads by Subhasish Biswas
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This special page shows all uploaded files.
| Date | Name | Thumbnail | Size | Description |
|---|---|---|---|---|
| 07:19, 14 February 2012 | 2011 Waldmann Angew.png (file) |  |
85 KB | first example of ps rection |
| 08:09, 10 February 2012 | 2008 Jacobsen OL.png (file) |  |
52 KB | Reverted to version as of 04:01, 20 January 2012 |
| 08:04, 10 February 2012 | 2005 Sui JMC.png (file) |  |
54 KB | potent and selective pyrimidinyl pyrroloquinolone PDE5 inhibitors were synthesised and evaluated for activity. |
| 07:42, 10 February 2012 | 2007 Jacobsen JACS2.png (file) |  |
40 KB | Asymmetric Cyclization of Hydroxylactams |
| 07:27, 10 February 2012 | 2007 Tanner Biochem.png (file) |  |
52 KB | Enzymatic Pictet-Spengler Reaction with norcoclaurine synthase and strictosidine synthase |
| 07:37, 9 February 2012 | 2010 Zhao OL.png (file) |  |
26 KB | an operationally simple diastereoselective cascade sequence for the preparation of indolo[2,3-R]quinolizidines was developed. |
| 07:27, 9 February 2012 | 2011 Bernardi ASC.png (file) |  |
40 KB | the first catalytic asymmetric Pictet– Spengler reaction using isatins as carbonyl components was developed |
| 08:56, 8 February 2012 | 2011 Rueping ASC.png (file) |  |
34 KB | a new efficient and general enantioselective multicomponent additioncyclization sequence using simple and commercially available starting materials such as cyclic 1,3-dicarbonyl compounds, unsaturated aldehydes and tryptamine was developed. |
| 08:37, 8 February 2012 | 2011 Tian OL.png (file) |  |
34 KB | a new strategy to extend the catalytic asymmetric Pictet�Spengler reaction to the construction of nitrogen-containing heterocycles by replacing the aldehyde with an imine was developed. |
| 08:17, 8 February 2012 | 2011 Volla RSC Ad.png (file) |  |
26 KB | a highly efficient and diastereoselective one-pot reaction of tryptamine with 1,3- dicarbonyl compounds and unsaturated aldehydes have been developed. |
| 07:57, 8 February 2012 | 2012 Sto¨ckigt JACS.png (file) |  |
45 KB | enzymatic catalysis leading to Piperazino-indole Framework |
| 07:29, 8 February 2012 | Pictet1.docx (file) |  |
44 KB | Pictet(Ame Pictet)-spengler(Theodor Spengler) reaction is a chemical reaction (specifically cycloaddition) in which a β-arylethylamine is made to react with a carbonyl group in the presence of an acid catalyst. In 1911, these two chemists have prepared 1 |
