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Dess-Martin Oxidation
Mechanism of the Dess-Martin Oxidation
Reference
| Original reference | J. Org. Chem. 1983, 48, 4155. |
|---|---|
| Wikipedia | link |
| Organic chemistry portal | link |
This step is from the synthesis of Aflatoxin B2 by Elias J. Corey. Show me the full synthesis.
0 °C to RT, 3 h
85 % (2 steps)
This step is from the synthesis of Penitrem D by Amos B. Smith, III. Show me the full synthesis.
RT, 3 h
90 %
This step is from the synthesis of Sarain A by Larry E. Overman. Show me the full synthesis.
0 °C, 90 min
This step is from the synthesis of Sarain A by Larry E. Overman. Show me the full synthesis.
0 °C, 20 min
This step is from the synthesis of Malayamycin A by Stephen Hanessian. Show me the full synthesis.
RT, 3.5 h
This step is from the synthesis of Zaragozic Acid C by David A. Evans. Show me the full synthesis.
RT, 8 h
94 %
This step is from the synthesis of Preussin by Won-Hun Han. Show me the full synthesis.
RT, 2 h
This step is from the synthesis of Dibromophakellstatin by David J. Austin. Show me the full synthesis.
RT, 2 h
This step is from the synthesis of Taxol by Isao Kuwajima. Show me the full synthesis.
RT, ON
77 %
This step is from the synthesis of Taxol by Isao Kuwajima. Show me the full synthesis.
RT, 60 min
92 %
This step is from the synthesis of Cortistatin A by Matthew D. Shair. Show me the full synthesis.
RT, 60 min
This step is from the synthesis of Ingenol by John L. Wood. Show me the full synthesis.
-40 to 10 °C, 90 min
74 %
This step is from the synthesis of Ingenol by Jeffrey D. Winkler. Show me the full synthesis.
0 °C to RT, 6 h
89 %
This step is from the synthesis of Ingenol by Jeffrey D. Winkler. Show me the full synthesis.
0 to 25 °C, 4 h
96 %
This step is from the synthesis of Grandisine D by Osamu Tamura. Show me the full synthesis.
4 °C to RT, 3 h
88 %
This step is from the synthesis of Morphine by James D. White. Show me the full synthesis.
RT, 60 min
96 %
This step is from the synthesis of Morphine by Catherine Guillou. Show me the full synthesis.
RT, 2 h
This step is from the synthesis of Morphine by Barry M. Trost. Show me the full synthesis.
75 °C to RT, 4.5 h
58 %
This step is from the synthesis of Pseudolaric Acid B by Barry M. Trost. Show me the full synthesis.
0 °C, 60 min
59 % (2 steps)
This step is from the synthesis of Pactamycin by Stephen Hanessian. Show me the full synthesis.
0 °C to RT, 2 h
96 %
This step is from the synthesis of Cylindrospermopsin by Barry B. Snider. Show me the full synthesis.
RT, 60 min
90 %
This step is from the synthesis of Caribenol A by Zhen Yang. Show me the full synthesis.
RT, 2 h
80 % (2 steps)
This step is from the synthesis of Caribenol A by Zhen Yang. Show me the full synthesis.
RT, 2 h
87 % (2 steps)
This step is from the synthesis of Oseltamivir by Masakatsu Shibasaki. Show me the full synthesis.
4 °C to RT, 25 min
90 %
This step is from the synthesis of Morphine by Gilbert Stork. Show me the full synthesis.
0 °C to RT, 3.5 h
This step is from the synthesis of Morphine by Gilbert Stork. Show me the full synthesis.
0 °C, 4.5 h
90 %
This step is from the synthesis of Strychnine by Tohru Fukuyama. Show me the full synthesis.
0 °C to RT, 35 min
69 % (3 steps)
This step is from the synthesis of Maritimol by Pierre Deslongchamps. Show me the full synthesis.
0 °C, 60 min
91 %
This step is from the synthesis of Maritimol by Pierre Deslongchamps. Show me the full synthesis.
0 °C to RT, 10 h
84 % (2 steps)
This step is from the synthesis of Dragmacidin F by Brian M. Stoltz. Show me the full synthesis.
RT, 3 min
90 %
This step is from the synthesis of Taiwaniaquinol B by Dirk Trauner. Show me the full synthesis.
RT, 5 min
90 %
This step is from the synthesis of Azadirachtin by Steven V. Ley. Show me the full synthesis.
13 °C to RT, 25 min
90 %
This step is from the synthesis of Thiarubrine A by Masato Koreeda. Show me the full synthesis.
RT, 30 min
91 %
This step is from the synthesis of Decarestrictine D by Ronaldo A. Pilli. Show me the full synthesis.
