Projects per year
Abstract
Hindered tertiary neopentyl glycol boronic esters can be prepared by using in situ lithiation–borylation of enantiopure secondary benzylic carbamates at −20 °C with full chirality transfer.
Original language | English |
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Pages (from-to) | 5289-5292 |
Number of pages | 4 |
Journal | Chemical Communications |
Volume | 52 |
Issue number | 30 |
Early online date | 22 Mar 2016 |
DOIs | |
Publication status | Published - 18 Apr 2016 |
Research Groups and Themes
- BCS and TECS CDTs
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Dive into the research topics of 'Full chirality transfer in the synthesis of hindered tertiary boronic esters under in situ lithiation–borylation conditions'. Together they form a unique fingerprint.Projects
- 3 Finished
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FRESCO: Efficient, Flexible Synthesis of Molecules with Tailored Shapes: from Photoswitchable Helices to anti-Cancer Compounds
Aggarwal, V. K. (Principal Investigator)
1/10/15 → 31/03/21
Project: Research
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3-month Core Capability for Chemistry Research
Crosby, J. (Principal Investigator)
1/01/13 → 1/04/13
Project: Research
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Changing the Synthesis Landscape with Boron at the Helm: from Chiral Organometallics to Assembly Line Synthesis
Aggarwal, V. K. (Principal Investigator)
14/05/12 → 13/01/18
Project: Research