Jones Oxidation
Mechanism of the Jones Oxidation
Reference
| Original reference | J. Chem. Soc. 1946, 39. |
|---|---|
| Wikipedia | link |
| Organic chemistry portal | link |
This step is from the synthesis of Quinine by Robert B. Woodward. Show me the full synthesis.

0 to 50 °C, ON
30% (2 steps)

This step is from the synthesis of Strychnine by Larry E. Overman. Show me the full synthesis.

-5 °C
97 %

This step is from the synthesis of Dodecahedrane by Leo A. Paquette. Show me the full synthesis.

5 °C, 2.5 h
92 %

This step is from the synthesis of Reserpine by Robert B. Woodward. Show me the full synthesis.

RT, 10 h
60 % (2 steps)

This step is from the synthesis of Chlorodysinosin A by Stephen Hanessian. Show me the full synthesis.

0 °C, 30 min
78 %

This step is from the synthesis of Phyllanthocin by David R. Williams. Show me the full synthesis.

RT, 45 min
75 %

This step is from the synthesis of Phyllanthocin by David R. Williams. Show me the full synthesis.

RT, 30 min
95 %

This step is from the synthesis of Gymnomitrol by Robert M. Coates. Show me the full synthesis.

92 % (2 steps)

This step is from the synthesis of Gymnomitrol by Robert M. Coates. Show me the full synthesis.

54 % (2 steps)

This step is from the synthesis of Gymnomitrol by Leo A. Paquette. Show me the full synthesis.

89 %

This step is from the synthesis of Gymnomitrol by Steven C. Welch. Show me the full synthesis.


This step is from the synthesis of Yohimbine by Eugene E. van Tamelen. Show me the full synthesis.

0 °C, 30 min
16 %

This step is from the synthesis of Dodecahedrane by Horst Prinzbach. Show me the full synthesis.
+ 
RT, 2.5 h
97 %
+ 
This step is from the synthesis of Luciduline by Wolfgang Oppolzer. Show me the full synthesis.

98 %

This step is from the synthesis of Quadrone by Steven D. Burke. Show me the full synthesis.

0 °C to RT, 8.5 h
98 %

This step is from the synthesis of Quadrone by Steven D. Burke. Show me the full synthesis.


This step is from the synthesis of Quadrone by Eiichi Yoshii. Show me the full synthesis.

RT, 30 min
49 % (2 steps)

This step is from the synthesis of Retigeranic Acid by Elias J. Corey. Show me the full synthesis.

93 % (2 steps)

This step is from the synthesis of Mesembrine by Maurice Shamma. Show me the full synthesis.

80 %

This step is from the synthesis of Daphnilactone A by Clayton H. Heathcock. Show me the full synthesis.

0 °C, 30 min

This step is from the synthesis of Nupharamine by Chihiro Kibayashi. Show me the full synthesis.

0 °C

This step is from the synthesis of Hirsutene by Takeshi Matsumoto. Show me the full synthesis.

95 %

This step is from the synthesis of Hirsutene by John B. Stothers. Show me the full synthesis.

RT, 2.5 h
72 % (3 steps)

This step is from the synthesis of Hirsutene by John B. Stothers. Show me the full synthesis.
+ 
RT
28 %

This step is from the synthesis of Hirsutene by Alan C. Weedon. Show me the full synthesis.

0 °C
47 % (2 steps)

This step is from the synthesis of Epibatidine by Alan Armstrong. Show me the full synthesis.

0 °C to RT, 100 min
92 %

This step is from the synthesis of Centrohexaindane by Dietmar Kuck. Show me the full synthesis.

RT, 12 h
94 %

This step is from the synthesis of Hirsutene by Daniel D. Sternbach. Show me the full synthesis.

0 °C, 60 min
97 %

This step is from the synthesis of Hirsutene by Daniel D. Sternbach. Show me the full synthesis.

RT, 45 min
95 %
