A chiral biselectrophile for efficient asymmetric synthesis in water
Research output: Contribution to journal › Article
Abstract
The development of an efficient asymmetric dihydroxylation of 1,6-dibromodiene afforded a chiral biselectrophilic diol that displayed highly useful reactivity in water, as demonstrated by a three-step, two-pot asymmetric synthesis of a highly functionalized tetrahydrofuran.
Details
| Authors | |
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| Organisations | |
| Research areas and keywords | Subject classification (UKÄ) – MANDATORY
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| Original language | English |
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| Pages (from-to) | 259-261 |
| Journal | Green Chemistry |
| Volume | 7 |
| Issue number | 5 |
| Publication status | Published - 2005 |
| Publication category | Research |
| Peer-reviewed | Yes |
Bibliographic note
The information about affiliations in this record was updated in December 2015.
The record was previously connected to the following departments: Organic chemistry (S/LTH) (011001240)
