15186-48-8
15186-48-8
Chemical Structure
(R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde
- CAS No.: 15186-48-8
- Formula:C6H10O3
- Molecular Weight:130.14
InChIKey: YSGPYVWACGYQDJ-YFKPBYRVSA-N
SMILES: O=C[C@@H]1OC(C)(OC1)C
Biological Activity: (R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde is an enantiopure starting material. Using (R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde as the raw material, olefin diols can be prepared via olefination and hydrolysis, which are further used for the synthesis of enantiopure perhydrofuro[3,4-b]pyrans and perhydrofuro[3,4-b]furans. (R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde can be applied to research related to enantioselective heterocyclic synthesis[1][2].
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(R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde | 96.55% | (R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde is an enantiopure starting material. Using (R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde as the raw material, olefin diols can be prepared via olefination and hydrolysis, which are further used for the synthesis of enantiopure perhydrofuro[3,4-b]pyrans and perhydrofuro[3,4-b]furans. (R)-(+)-2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde can be applied to research related to enantioselective heterocyclic synthesis. | ||||||||||||||||||||
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References
- [1]. Bagnoli L, et al. Selenium promoted enantioselective synthesis of spiroketals. 9th International Electronic Conference on Synthetic Organic Chemistry (ECSOC-9). 2005.
- [2]. Tiecco M, et al. Synthesis of enantiomerically pure perhydrofuro[3,4-b]pyrans and perhydrofuro[3,4-b]furans. Tetrahedron: Asymmetry. 2004;15:1949-1955.
