Weight | 98.101 g/mol |
---|---|
Formula | C5H6O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
547-65-9 (547-65-9)
tulipalin A · alpha-methylene gamma-butyrolactone
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- Cross-metathesis between alpha-methylene-gamma-butyrolactone and olefins: a dramatic additive effect. (Organic Letters, 2007)
- New applications of the Mannich reaction. Use of dimethyl(methylene)ammonium trifluoroacetate for regiospecific carbanion quenching. A new route to .alpha.-methylene-.gamma.-butyrolactone (Journal of the American Chemical Society, 1977)
- An efficient synthesis of .gamma.-methylene-.gamma.-butyrolactone (.alpha.'-angelicalactone). Application to the synthesis of deoxyobtusilactone and deoxyisoobtusilactone (Journal of Organic Chemistry, 1978)
- Practical synthesis of .alpha.-methylene-.gamma.-butyrolactone (Journal of Organic Chemistry, 1974)
- Synthesis of a model hapten with cyclohexanediol and .alpha.-methylene-.gamma.-butyrolactone groups, a synthetic analog of poison ivy and tulipalin allergens connected with a carbon chain (Journal of Organic Chemistry, 1988)
- Double-head haptens. Synthesis of and experimentally induced contact sensitivity to substances containing two unrelated haptens, pyrocatechol and alpha-methylene-gamma-butyrolactone, in the same molecule. (Journal of Medicinal Chemistry, 1982)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - tulipalin A
- alpha-methylene gamma-butyrolactone
-
SMILESC=C1CCOC1=O
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InChIKeyGSLDEZOOOSBFGP-UHFFFAOYSA-N
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