Loading...
Please wait, while we are loading the content...
Similar Documents
Enantioselective synthesis of dialkylated N-heterocycles by palladium-catalyzed allylic alkylation.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Numajiri, Yoshitaka Jiménez-Osés, Gonzalo Wang, Bo Houk, Kendall N. Stoltz, Brian M. |
| Copyright Year | 2015 |
| Abstract | The enantioselective synthesis of α-disubstituted N-heterocyclic carbonyl compounds has been accomplished using palladium-catalyzed allylic alkylation. These catalytic conditions enable access to various heterocycles, such as morpholinone, thiomorpholinone, oxazolidin-4-one, 1,2-oxazepan-3-one, 1,3-oxazinan-4-one, and structurally related lactams, all bearing fully substituted α-positions. Broad functional group tolerance was explored at the α-position in the morpholinone series. We demonstrate the utility of this method by performing various transformations on our useful products to readily access a number of enantioenriched compounds. |
| Starting Page | 827 |
| Ending Page | 828 |
| Page Count | 2 |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | http://stoltz2.caltech.edu/publications/169-s-2015.pdf |
| PubMed reference number | 25714704v1 |
| Alternate Webpage(s) | https://doi.org/10.1021/ol503425t |
| DOI | 10.1021/ol503425t |
| Journal | Organic letters |
| Volume Number | 17 |
| Issue Number | 5 |
| Language | English |
| Access Restriction | Open |
| Subject Keyword | Alkylation Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone Lactams Palladium carbonyl compound cell transformation |
| Content Type | Text |
| Resource Type | Article |