| Weight | 155.197 g/mol |
|---|---|
| Formula | C8H13NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
RETRONECINE (480-85-3)
Score:
#1238 in Biochemistry
,
#3073 in Biology
,
#3842 in Chemistry
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- New General Asymmetric Synthesis of Versatile -Alkylated Butenolides and Its Application to Expeditious Synthesis of the Chiral Geissman-Waiss Lactones Useful for (+)-Retronecine Synthesis. (Journal of Organic Chemistry, 1989)
- Stereospecific synthesis of retronecine by imidate methylide cycloaddition (Journal of the American Chemical Society, 1980)
- Nonstabilized imidate ylides by the desilylation method: A route to the pyrrolizidine alkaloids retronecine and indicine (Journal of Organic Chemistry, 1985)
- Functionalized nitrones. A highly stereoselective and regioselective synthesis of dl-retronecine (Journal of the American Chemical Society, 1980)
- Synthetic studies on pyrrolizidine alkaloids. 1. ()-Heliotridine and ()-retronecine via intramolecular dienophile transfer [8] (Journal of the American Chemical Society, 1980)
- The Total Synthesis of (+)-Retronecine (Journal of Organic Chemistry, 1962)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CN2CC=C(C2C1O)CO
-
InChIKeyHJSJELVDQOXCHO-UHFFFAOYSA-N
- Pubchem - RETRONECINE
- Wikipedia - retronecine
Retronecine is a pyrrolizidine alkaloid found in a variety of plants in the genera Senecio and Crotalaria, and the family Boraginaceae. It is the most common central core for other pyrrolizidine alkaloids.
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RETRONECINE
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