Description
Allyl b-D-Lactose (Highly Pure)
| Catalog number: | B2012996 |
| Lot number: | Batch Dependent |
| Expiration Date: | Batch dependent |
| Amount: | 100 mg |
| Molecular Weight or Concentration: | 382.4 g/mol |
| Supplied as: | Lyophilized Powder |
| Applications: | molecular tool for various biochemical applications |
| Storage: | RT |
| Keywords: | Lactose |
| Grade: | Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity>18 M-cm) and are filtered through 0.22 um. |
References
- Junk L, Kazmaier U. The Allylic Alkylation of Ketone Enolates ChemistryOpen. 2020 Sep 10;9(9):929-952.
- Horino Y, Korenaga T. Versatile Reactivity of Metalloid-Substituted -Allylpalladium Species Chem Rec. 2021 Dec;21(12):3911-3924.
- Jeon J, Cheon CH. Asymmetric Total Synthesis of Iheyamine B Org Lett. 2022 Oct 7;24(39):7128-7133.
- Ariyarathna Y, Tunge JA. Multicomponent decarboxylative allylations Chem Commun (Camb). 2014 Nov 21;50(90):14049-52.
- Rossi-Ashton JA, Clarke AK, Donald JR, Zheng C, Taylor RJK, Unsworth WP, You SL. Iridium-Catalyzed Enantioselective Intermolecular Indole C2-Allylation Angew Chem Int Ed Engl. 2020 May 4;59(19):7598-7604.
- Ou P, Zhu L, Yu Y, Ma L, Huang X. Palladium-Catalyzed Three-Component Selective Aminoallylation of Diazo Compounds Org Lett. 2022 Jun 17;24(23):4160-4164.
- Tang Q, Fu K, Ruan P, Dong S, Su Z, Liu X, Feng X. Asymmetric Catalytic Formal 1,4-Allylation of ,-Unsaturated -Ketoesters: Allylboration/Oxy-Cope Rearrangement Angew Chem Int Ed Engl. 2019 Aug 19;58(34):11846-11851.
- Spaltenstein P, Cummins EJ, Yokuda KM, Kowalczyk T, Clark TB, ONeil GW. Chemoselective Carbonyl Allylations with Alkoxyallylsiletanes J Org Chem. 2019 Apr 5;84(7):4421-4428.
- Zhang ZZ, Liao G, Chen HM, Shi BF. Thioamide-Directed Cp*Co(III)-Catalyzed C-H Allylation of Ferrocenes Org Lett. 2021 Apr 2;23(7):2626-2631.
