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A THEORETICAL INVESTIGATION OF SOME STEREOELECTRONIC EFFECTSELLIOTT RJ; RICHARDS WG.1982; C.S. PERKIN TRANS. 2; ISSN 0300-9580; GBR; DA. 1982; NO 8; PP. 1005-1008; BIBL. 16 REF.Article

Unimolecular decomposition and vibrationally induced electron autodetachment of acetone enolate ionFOSTER, R. F; TUMAS, W; BRAUMAN, J. I et al.The Journal of chemical physics. 1983, Vol 79, Num 9, pp 4644-4646, issn 0021-9606Article

On the reactivity of dimsyl anion with aryl radicalsALONSO, R. A; ROSSI, R. A.Tetrahedron letters. 1985, Vol 26, Num 47, pp 5763-5764, issn 0040-4039Article

Studies on SRN1 reactions―91: A new access to the isoquinoline ring systemBEUGELMANS, R; CHASTANET, J; ROUSSI, G et al.Tetrahedron (Oxford. Print). 1984, Vol 40, Num 2, pp 311-314, issn 0040-4020Article

INDOLE SYNTHESIS VIA SRN 1 REACTIONSBARD RR; BUNNETT JF.1980; J. ORG. CHEM.; USA; DA. 1980; VOL. 45; NO 8; PP. 1546-1547; BIBL. 8 REF.Article

SOLVENT EFFECTS IN HETEROAROMATIC SRN1 REACTIONSMOON MP; WOLFE JF.1979; J. ORG. CHEM.; USA; DA. 1979; VOL. 44; NO 23; PP. 4081-4085; BIBL. 31 REF.Article

Formation de l'ion énolate [CH3COCHCOCH3]- par condensation en phase gazeuse = Formation of [CH3COCHCOCH3]- enolate anion by gaseous phase condensationBOUCHOUX, G; HOPPILLIARD, Y.Tetrahedron letters. 1987, Vol 28, Num 39, pp 4537-4540, issn 0040-4039Article

The novel formation of an acetone enolate complex via the addition of methyllithium to the acylrhodium(I) compound Rh(COMe)(CO)(triphos) (triphos = MeC(CH2PPh2)3)JOHNSTON, G. G; BAIRD, M. C.Journal of organometallic chemistry. 1986, Vol 314, Num 1-2, pp C51-C54, issn 0022-328XArticle

SRN1 MECHANISM IN BIFUNCTIONAL SYSTEMSALONSO RA; ROSSI RA.1980; J. ORG. CHEM.; ISSN 0022-3263; USA; DA. 1980; VOL. 45; NO 23; PP. 4760-4763; BIBL. 13 REF.Article

REACTIONS OF CARBON NUCLEOPHILES WITH 4-PHENYL- AND 4-TERT-BUTYL-5-HALOGENOPYRIMIDINES. ON THE OCCURRENCE OF AN SRN1 MECHANISMOOSTVEEN EA; VAN DER PLAS HC.1979; REC. TRAV. CHIM. PAYS-BAS; NLD; DA. 1979; VOL. 98; NO 7-8; PP. 441-444; BIBL. 32 REF.Article

An effective method for controlling 3,4-stereochemistry of aldols. Direct preparation of optically active 2,3-anti-3-hydroxy-2-methyl carbonyl compoundsSATO, F; KUSAKABE, M; KATO, T et al.Journal of the Chemical Society. Chemical communications. 1984, Num 20, pp 1331-1332, issn 0022-4936Article

SUBSTITUTION NUCLEOPHILE AROMATIQUE RADICALAIRE. I: SYNTHESE DIRECTE DE 4-AZA-INDOLES DANS DES CONDITIONS NON ACIDES ET DOUCESBEUGELMANS R; BOUDET B; QUINTERO L et al.1980; TETRAHEDRON LETTERS; GBR; DA. 1980; VOL. 21; NO 20; PP. 1943-1944; ABS. ENG; BIBL. 8 REF.Article

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