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Explaining Regiodiv...
Explaining Regiodivergent Vinylations with Vinylbenziodoxolones
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- Di Tommaso, Ester Maria (författare)
- Stockholms universitet,Institutionen för organisk kemi
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Norrby, Per-Ola (författare)
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- Olofsson, Berit (författare)
- Stockholms universitet,Institutionen för organisk kemi
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(creator_code:org_t)
- 2022-07-08
- 2022
- Engelska.
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Ingår i: Angewandte Chemie International Edition. - : Wiley. - 1433-7851 .- 1521-3773. ; 61:34
- Relaterad länk:
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https://doi.org/10.1...
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visa fler...
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- Vinylbenziodoxolones have recently been identified as efficient hypervalent iodine(III) reagents for electrophilic vinylations under transition metal-free conditions. Their unique reactivity allows synthesis of either internal or terminal alkenes, depending on the nucleophile class. This paper constitutes the first mechanistic investigation of VBX vinylations, and makes use of NMR studies, deuterium labelling and computations to rationalize the observed regio- and stereochemical outcome. Internal alkene formation in S-vinylation was found to proceed through the ligand coupling mechanism typical of diaryliodonium salts, whereas terminal alkene formation in P-vinylations took place via a phosphinous acid-coordinated VBX complex, which underwent concerted deprotonation and Michael-type addition. Subsequent base-assisted protonation and E2 elimination delivered the terminal alkene. The findings can be used to predict the regioselectivity in vinylations of other nucleophile classes.
Ämnesord
- NATURVETENSKAP -- Kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences (hsv//eng)
Nyckelord
- Alkenes
- Density Functional Calculations
- Deuterium Labelling
- Hypervalent Compounds
- Regioselectivity
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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