000 | 02937cab a22005417i 4500 | ||
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001 | 7381857 | ||
003 | OSt | ||
005 | 20250628165017.0 | ||
006 | m d | | ||
007 | cr| nn|||||||| | ||
008 | s2015 xxk|||||s|||||||||||eng d | ||
035 | _a(Uk)013331807 | ||
035 | _a(IssueARKID)ark:/81055/vdc_100025029023.0x0001cb | ||
035 | _a(oaiARKID)oai:ark:/81055/vdc_100025029148.0x000001 | ||
035 | _aark:/81055/vdc_100025029061.0x000064 | ||
040 |
_dStEdNL _c0 |
||
100 | _4Porter, Eleanor H. | ||
245 | 0 |
_aPolly-Anna _cPorter, Eleanor H |
|
260 |
_aBoston _bGrosset & Dunlap, _c1913 |
||
300 |
_a310p _bill. _c19.5 cm |
||
500 | _aIn: Advanced synthesis & catalysis, Vol. 357, no. 6 ( 2015), p.1245-1257. | ||
506 |
_aOwing to Legal Deposit regulations this resource may only be accessed from within National Library of Scotland. For more information contact enquiries@nls.uk _5StEdNL |
||
520 | _a Abstract Utilizing ‘off the shelf’ commercially available, cheap, small synthetic molecules that mimic the efficient mediation of important bioreactions utilized by Nature is not only highly sought after but also currently highly topical. This paper details our preliminary efforts at developing a unique base‐ and metal‐free phase‐transfer‐mediated malonic acid thioester (MAHT) ‘activation protocol’ that efficiently generates (*)‐(Sb‐(Bthioesters. Our bioinspired aldol process is exceptionally mild, conducted under near neutral pH reaction conditions, does not require an inert, oxygen‐free atmosphere or anhydrous reaction conditions and is highly atom‐economic. Exemplifying the utility of our protocol, the synthesis of an array of structurally and functionally diverse (*)‐(Sb‐(Bhydroxy thioesters equipped with highly prized functionality, i.e., chlorine, bromine, fluorine, nitrile and nitro groups, is reported, as is the diastereoselective potential of this important reaction. | ||
590 | _aThis catalogue record is generated as a result of Non Print Legal Deposit processing | ||
650 | 4 | _aCatalysis. | |
650 | 4 | _aOrganic compounds. | |
650 | 4 | _aSynthesis. | |
650 | 4 | _aChemistry. | |
650 | 4 | _aChemistry, Technical. | |
650 | 4 | _aChemistry. | |
650 | 4 | _aCatalysis. | |
650 | 4 | _aTechnology, Pharmaceutical. | |
700 | 1 | _aBew, Sean P. | |
700 | 1 | _aStephenson, G. Richard. | |
700 | 1 | _aRouden, Jacques. | |
700 | 1 | _aAshford, Polly‐Anna. | |
700 | 1 | _aBourane, Manuel. | |
700 | 1 | _aCharvet, Agathe. | |
700 | 1 | _aDalstein, Virginie M. D. | |
700 | 1 | _aJauseau, Raphael. | |
700 | 1 | _aHiatt‐Gipson, G. D. | |
700 | 1 | _aMartinez‐Lozano, Luis A. | |
773 | 0 |
_tAdvanced synthesis & catalysis _x1615-4169 |
|
773 | 0 | _w(IssueARKID)ark:/81055/vdc_100025029023.0x0001cb | |
856 | 4 | 0 |
_uhttps://nls.ldls.org.uk/welcome.html?ark:/81055/vdc_100025029061.0x000064 _zView item |
942 |
_2fc _cFIC |
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999 |
_c7716 _d7716 |