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Tandem Beckmann and Huisgen–White rearrangement of the
9-azabicyclo[3.3.1]nonan-3-one system. Part 2.1 The second
mode of the rearrangement leading to 6-(prop-1-enyl)piperidin-2-ylacetic
acid, a versatile intermediate for the syntheses of piperidine alkaloids
(+)-pinidine and (+)-monomorine I
. Osamu Muraoka, Bao-Zhong Zheng, Kazuhito Okumura, Emi Tabata, Genzoh Tanabe, Michinori Kubo
, J. Chem. Soc., Perkin Trans. 1
, 1997
, 113
- Syntheses with isoxazoles. Part II. Rearrangement of isoxazolo[2,3-a]-pyridinium salts into 5,6-dihydro-4H-furo[3,2-b]pyridin-2-ones. R. H. Good, Gurnos Jones, J. R. Phipps
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 2441
- Complementary enantioselective approaches to the quinolizidine alkaloids lupinine and epilupinine by enolate Claisen rearrangements or direct allylation of piperidin-2-ylacetic acid derivatives. Christopher Morley, David W. Knight, Andrew C. Share
, J. Chem. Soc., Perkin Trans. 1
, 1994
, 2903
- A product from the reaction of pyridine with acetic anhydride. Ian Fleming, J. B. Mason
, J. Chem. Soc. C
, 1969
, 2509
- Contents pages
, J. Chem. Soc., Perkin Trans. 1
, 1994
, P179
- Indolizidine and quinolizidine alkaloids. J. P. Michael
, Nat. Prod. Rep.
, 1991
, 8
, 553
- Index of subjects
, J. Chem. Soc., Abstr.
, 1902
, 82
, B811
- Organic chemistry
, J. Chem. Soc., Abstr.
, 1902
, 82
, A333