Weight | 87.122 g/mol |
---|---|
Formula | C4H9NO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Pyrrolidin-3-ol (40499-83-0)
4-hydroxypyrrolidine
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- The Enantioselective Michael Addition of Thiols to Cycloalkenones by Using (2S, 4S)-2-Anilinomethyl-1-ethyl-4-hydroxypyrrolidine as Chiral Catalyst (Bulletin of the Chemical Society of Japan, 1982)
- Synthesis of 2(R), 5(R)-bis(hydroxymethyl)-3(R), 4(R)-di-hydroxypyrrolidine: a novel glycosidase inhibitor (Journal of Organic Chemistry, 1985)
- Enzymatic ammonolysis of ethyl ()-4-chloro-3-hydroxybutanoate. Chemoenzymatic syntheses of both enantiomers of pyrrolidin-3-ol and 5-(chloromethyl)-1,3-oxazolidin-2-one (Tetrahedron-asymmetry, 1999)
- Synthesis of 1-aza-C-nucleosides from (3R,4R)-4-(hydroxymethyl)pyrrolidin-3-ol (Tetrahedron, 2001)
- A Practical Large-Scale Synthesis of (3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol via Asymmetric 1,3-Dipolar Cycloaddition (Organic Process Research & Development, 2005)
- A 4HydroxypyrrolidineCatalyzed Mannich Reaction of Aldehydes: Control of antiSelectivity by Hydrogen Bonding Assisted by Brnsted Acids (Chemistry: A European Journal, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-hydroxypyrrolidine
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SMILESC1CNCC1O
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InChIKeyJHHZLHWJQPUNKB-UHFFFAOYSA-N
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