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Iridium-catalyzed asymmetric allylation of sodium triisopropylsilanethiolate: a new way to form chiral thiols.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Huang, Weiqing Zheng, Shengcai Tang, Jialiang Zhao, Xiaoming |
| Copyright Year | 2011 |
| Abstract | The iridium phosphoramidite complex-promoted regio- and enantioselective reaction of allylic carbonates with sodium triisopropylsilanethiolate produced allylic sulfides in 40-77% yields with up to 97 : 3 (branched : linear) and 89% ee, which were readily transformed into chiral thiol in 68% yield with 87% ee or disulfides with two chiral C-S bond centers in 40-73% yields with up to 90 : 10 dr and 99% ee. |
| Starting Page | 47 |
| Ending Page | 55 |
| Page Count | 9 |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/ob/c1/c1ob06332d/c1ob06332d.pdf |
| PubMed reference number | 21968518v1 |
| Alternate Webpage(s) | https://doi.org/10.1039/c1ob06332d |
| DOI | 10.1039/c1ob06332d |
| Journal | Organic & biomolecular chemistry |
| Volume Number | 9 |
| Issue Number | 22 |
| Language | English |
| Access Restriction | Open |
| Subject Keyword | Carbonates Disulfides Eighty Nine Ethinyl Estradiol Iridium Ninety Nine Sodium Sulfhydryl Compounds Sulfides phosphoramidite |
| Content Type | Text |
| Resource Type | Article |