ethyl 1,3-dithiolane-2-carboxylate
ethyl 1,3-dithiolane-2-carboxylate structure
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Common Name | ethyl 1,3-dithiolane-2-carboxylate | ||
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| CAS Number | 20461-99-8 | Molecular Weight | 178.27200 | |
| Density | 1.249 g/mL at 25 °C(lit.) | Boiling Point | 85 °C0.1 mm Hg(lit.) | |
| Molecular Formula | C6H10O2S2 | Melting Point | N/A | |
| MSDS | USA | Flash Point | >230 °F | |
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General strategy for the syntheses of corynanthe, tacaman, and oxindole alkaloids.
J. Org. Chem. 71(17) , 6547-61, (2006) We report herein the total synthesis of the corynanthe alkaloid dihydrocorynantheol and the formal syntheses of the indole alkaloids tacamonine, rhynchophylline, and hirsutine. The strategies for assembling the corynanthe and tacaman skeletal frameworks compr... |
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Stereodivergent synthesis of enantiopure cis- and trans-3-Ethyl-4-piperidineacetates.
Org. Lett. 4(16) , 2787-90, (2002) [reaction: see text] Starting from a common chiral bicyclic lactam 11, enantiopure trans- or cis-3-ethyl-4-piperidineacetate derivatives are obtained by conjugate addition of an enolate or a cuprate to the unsaturated lactams 12 or 18, respectively. |
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H. Paulson, W. Koebernick
Chem. Ber. 110 , 2127, (1977)
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M. Kato et al.
Chem. Lett. , 213, (1984)
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L.A. Flippin, M.A. Dombroski
Tetrahedron Lett. 26 , 2977, (1985)
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