-
2
-
-
0141670408
-
The directed lithiation of benzenoid aromatic systems
-
Wheatley, A. E. H. The directed lithiation of benzenoid aromatic systems. Eur. J. Inorg. Chem., 2003, 3291-3303.
-
(2003)
Eur. J. Inorg. Chem
, pp. 3291-3303
-
-
Wheatley, A.E.H.1
-
3
-
-
69949083590
-
Direct metalation of methoxymethyl arylmethyl ethers: A tin-free approach to the generation of α-alkoxyalkoxysubstituted aryllithiums
-
Azzena, U.; Mocci, S.; Pisano, L. Direct metalation of methoxymethyl arylmethyl ethers: a tin-free approach to the generation of α-alkoxyalkoxysubstituted aryllithiums. J. Organomet. Chem., 2009, 694, 3619-3625.
-
(2009)
J. Organomet. Chem
, vol.694
, pp. 3619-3625
-
-
Azzena, U.1
Mocci, S.2
Pisano, L.3
-
4
-
-
19344364434
-
Intramolecular dissociative electron transfer
-
Maran, F.; Antonello, S. Intramolecular dissociative electron transfer. Chem. Soc. Rev., 2005, 34, 418-428.
-
(2005)
Chem. Soc. Rev
, vol.34
, pp. 418-428
-
-
Maran, F.1
Antonello, S.2
-
5
-
-
1542411152
-
Electron transfer and bond breaking. Examples of passage from a sequential to a concerted mechanism in the electrochemical reductive cleavage of arylmethyl halides
-
Andrieux, C. P.; Le Gorande, A.; Savéant, J.-M. Electron transfer and bond breaking. Examples of passage from a sequential to a concerted mechanism in the electrochemical reductive cleavage of arylmethyl halides. J. Am. Chem. Soc., 1992, 114, 6892-6904.
-
(1992)
J. Am. Chem. Soc
, vol.114
, pp. 6892-6904
-
-
Andrieux, C.P.1
Le Gorande, A.2
Savéant, J.-M.3
-
6
-
-
0001708577
-
Electron apportionment in cleavage of radical anions. 1. Nitro-substituted benzyl phenyl ethers
-
Maslak, P.; Guthrie, R. D. Electron apportionment in cleavage of radical anions. 1. Nitro-substituted benzyl phenyl ethers. J. Am. Chem. Soc., 1986, 108, 2628-2636
-
(1986)
J. Am. Chem. Soc
, vol.108
, pp. 2628-2636
-
-
Maslak, P.1
Guthrie, R.D.2
-
7
-
-
33845374272
-
Electron apportionment in cleavage of radical anions. 2. Naphthylmethyl phenyl ethers vs. naphthyl benzyl ethers
-
Maslak, P.; Guthrie, R. D. Electron apportionment in cleavage of radical anions. 2. Naphthylmethyl phenyl ethers vs. naphthyl benzyl ethers. J. Am. Chem. Soc., 1986, 108, 2637-2640.
-
(1986)
J. Am. Chem. Soc
, vol.108
, pp. 2637-2640
-
-
Maslak, P.1
Guthrie, R.D.2
-
8
-
-
84962468728
-
A theoretical study of the competitive homolytic/heterolytic aniomesolytic cleavages of C-O alkyl ether bonds
-
Asensio, X.; Gonzalez-Lafont, A.; Marquet, J.; Lluch, J. M. A theoretical study of the competitive homolytic/heterolytic aniomesolytic cleavages of C-O alkyl ether bonds. J. Org. Chem., 2005, 70, 540-548.
-
(2005)
J. Org. Chem
, vol.70
, pp. 540-548
-
-
Asensio, X.1
Gonzalez-Lafont, A.2
Marquet, J.3
Lluch, J.M.4
-
9
-
-
0037393779
-
Bond dissociation energies of organic molecules
-
Blanksby, S. J.; Ellison, G. B. Bond dissociation energies of organic molecules. Acc. Chem. Res., 2003, 36, 255-263.
-
(2003)
Acc. Chem. Res
, vol.36
, pp. 255-263
-
-
Blanksby, S.J.1
Ellison, G.B.2
-
10
-
-
0009515015
-
Dimer formation during reactions of benzylic halides with lithium naphthalene and mechanisms of dimer formation from reactions of benzylic halides with benzylic carbanions
-
Zieger, H. E.; Angres, I.; Mathisen, D. Dimer formation during reactions of benzylic halides with lithium naphthalene and mechanisms of dimer formation from reactions of benzylic halides with benzylic carbanions. J. Am. Chem. Soc., 1976, 98, 2580-2585.
-
(1976)
J. Am. Chem. Soc
, vol.98
, pp. 2580-2585
-
-
Zieger, H.E.1
Angres, I.2
Mathisen, D.3
-
11
-
-
0030820304
-
Cumyl phenyl sulfide forms bicumyl instead of cumyllithium upon reductive lithiation. Thiophenoxide as a leaving group in nucleophilic substitution by SET
-
Kulkarni, V.; Cohen, T. Cumyl phenyl sulfide forms bicumyl instead of cumyllithium upon reductive lithiation. Thiophenoxide as a leaving group in nucleophilic substitution by SET. Tetrahedron, 1997, 53, 12089-12100.
-
(1997)
Tetrahedron
, vol.53
, pp. 12089-12100
-
-
Kulkarni, V.1
Cohen, T.2
-
12
-
-
37049073704
-
Arene-catalysed lithiation reactions with lithium at low temperature
-
Yus, M.; Ramón, D. J. Arene-catalysed lithiation reactions with lithium at low temperature. J. Chem. Soc., Chem. Commun., 1991, 398-400.
-
(1991)
J. Chem. Soc., Chem. Commun
, pp. 398-400
-
-
Yus, M.1
Ramón, D.J.2
-
13
-
-
33847087012
-
Alkyllithium reagents from alkyl halides and lithium radical anions
-
Freeman, P. K.; Hutchinson, L. L. Alkyllithium reagents from alkyl halides and lithium radical anions. J. Org. Chem., 1980, 45, 1924-1930.
-
(1980)
J. Org. Chem
, vol.45
, pp. 1924-1930
-
-
Freeman, P.K.1
Hutchinson, L.L.2
-
14
-
-
0010318348
-
-
King, R. B., Eisch, J. J., Eds, Elsevier Science B. V.: Amsterdam
-
Cohen, T.; Sherbine, J. P.; Hutchins, R. R.; Lin, M.-T. Organomet. Synth., King, R. B., Eisch, J. J., Eds; Elsevier Science B. V.: Amsterdam, 1986, Vol. 3, pp. 361-368.
-
(1986)
Organomet. Synth
, vol.3
, pp. 361-368
-
-
Cohen, T.1
Sherbine, J.P.2
Hutchins, R.R.3
Lin, M.-T.4
-
15
-
-
70649083233
-
The superiority of properly prepared lithium 1-N,N-dimethylaminonaphthalenide (LDMAN) over other aromatic radical-anions for the generation of organolithiums by reductive lithiation
-
Ivanov, R.; Marek, I.; Cohen, T. The superiority of properly prepared lithium 1-N,N-dimethylaminonaphthalenide (LDMAN) over other aromatic radical-anions for the generation of organolithiums by reductive lithiation. Tetrahedron Lett., 2010, 51, 174-176.
-
(2010)
Tetrahedron Lett
, vol.51
, pp. 174-176
-
-
Ivanov, R.1
Marek, I.2
Cohen, T.3
-
16
-
-
0034829936
-
Use of aromatic radical-anions in the absence of THF. Tandem formation and cyclization of benzyllithiums derived from the attack of homo- and bishomoallyllithiums on α-methylstyrenes: Two-pot synthesis of cuparene
-
for alternative solvents, see: dimethyl ether:
-
For alternative solvents, see: dimethyl ether: Cohen, T.; Kreethadumrongdat, T.; Liu, X.; Kulkarni, V. Use of aromatic radical-anions in the absence of THF. Tandem formation and cyclization of benzyllithiums derived from the attack of homo- and bishomoallyllithiums on α-methylstyrenes: two-pot synthesis of cuparene. J. Am. Chem. Soc., 2001, 123, 3478-3483
-
(2001)
J. Am. Chem. Soc
, vol.123
, pp. 3478-3483
-
-
Cohen, T.1
Kreethadumrongdat, T.2
Liu, X.3
Kulkarni, V.4
-
17
-
-
19444365357
-
Medium-dependent lithiated side products in the reductive lithiation of allylic phenyl thioethers. Diethyl ether versus tetrahydrofuran
-
diethyl ether
-
diethyl ether: Screttas, C. G.; Heropoulos, G. A.; Micha-Screttas, M.; Steele, B. R. Medium-dependent lithiated side products in the reductive lithiation of allylic phenyl thioethers. Diethyl ether versus tetrahydrofuran. Tetrahedron Lett., 2005, 46, 4357-4360.
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 4357-4360
-
-
Screttas, C.G.1
Heropoulos, G.A.2
Micha-Screttas, M.3
Steele, B.R.4
-
18
-
-
37049130364
-
Stoicheiometry and synthetic utility of the reaction of alkyl halides with lithium dihydronaphthylide
-
for a selection of general literature on the reductive metalation procedure, see
-
For a selection of general literature on the reductive metalation procedure, see: Screttas, C. G. Stoicheiometry and synthetic utility of the reaction of alkyl halides with lithium dihydronaphthylide. J. Chem. Soc., Chem. Commun., 1972, 752-753.
-
(1972)
J. Chem. Soc., Chem. Commun
, pp. 752-753
-
-
Screttas, C.G.1
-
19
-
-
0000644216
-
Hydrolithiation of α-olefins by a regiospecific two-step process. Transformation of alkyl phenyl sulfides to alkyllithium reagents
-
Screttas, C. G.; Micha-Screttas, M. Hydrolithiation of α-olefins by a regiospecific two-step process. Transformation of alkyl phenyl sulfides to alkyllithium reagents. J. Org. Chem., 1978, 43, 1064-1071.
-
(1978)
J. Org. Chem
, vol.43
, pp. 1064-1071
-
-
Screttas, C.G.1
Micha-Screttas, M.2
-
20
-
-
33845560841
-
Markownikoff two-step hydrolithiation of α-olefins. Transformation of secondary and tertiary alkyl phenyl sulfides to the relevant alkyllithium reagents
-
Screttas, C. G.; Micha-Screttas, M. Markownikoff two-step hydrolithiation of α-olefins. Transformation of secondary and tertiary alkyl phenyl sulfides to the relevant alkyllithium reagents. J. Org. Chem., 1979, 44, 713-719.
-
(1979)
J. Org. Chem
, vol.44
, pp. 713-719
-
-
Screttas, C.G.1
Micha-Screttas, M.2
-
21
-
-
0001166977
-
Organoalkali compounds by radical anion induced reductive metalation of phenyl thioethers
-
Cohen, T.; Bhupathy, M. Organoalkali compounds by radical anion induced reductive metalation of phenyl thioethers. Acc. Chem. Res., 1989, 22, 152-161.
-
(1989)
Acc. Chem. Res
, vol.22
, pp. 152-161
-
-
Cohen, T.1
Bhupathy, M.2
-
22
-
-
0010895435
-
-
Block, E., Ed.; VCH: New York
-
Cohen, T. Heteroatom Chemistry; Block, E., Ed.; VCH: New York, 1990; pp. 129-142.
-
(1990)
Heteroatom Chemistry
, pp. 129-142
-
-
Cohen, T.1
-
23
-
-
0030496093
-
Arene-catalysed lithiation reactions
-
Yus, M. Arene-catalysed lithiation reactions. Chem. Soc. Rev., 1996, 155-161;
-
(1996)
Chem. Soc. Rev
, pp. 155-161
-
-
Yus, M.1
-
24
-
-
0039994017
-
Novel electrontransfer reactions mediated by alkali metals complexed by macrocyclic ligand
-
Jedliński, Z. Novel electrontransfer reactions mediated by alkali metals complexed by macrocyclic ligand. Acc. Chem. Res., 1998, 31, 55-61.
-
(1998)
Acc. Chem. Res
, vol.31
, pp. 55-61
-
-
Jedliński, Z.1
-
25
-
-
0033979918
-
New methodologies based on arene-catalyzed lithiation reactions and their application to synthetic organic chemistry
-
Ramón, D. J.; Yus, M. New methodologies based on arene-catalyzed lithiation reactions and their application to synthetic organic chemistry. Eur. J. Org. Chem., 2000, 225-237.
-
(2000)
Eur. J. Org. Chem
, pp. 225-237
-
-
Ramón, D.J.1
Yus, M.2
-
26
-
-
0034904455
-
From arene-catalyzed lithiation to other synthetic adventures
-
Yus, M. From arene-catalyzed lithiation to other synthetic adventures. Synlett, 2001, 1197-1205.
-
(2001)
Synlett
, pp. 1197-1205
-
-
Yus, M.1
-
27
-
-
40749138993
-
Reductive opening of heterocycles with lithium metal as a source of functionalised organolithium compounds
-
Attanasi, O. A., Spinelli, D., Eds., Italian Society of Chemistry: Rome
-
Yus, M.; Foubelo, F. Reductive opening of heterocycles with lithium metal as a source of functionalised organolithium compounds. Attanasi, O. A., Spinelli, D., Eds.; in Targets in Heterocyclic Systems; Italian Society of Chemistry: Rome, 2002, Vol. 6, pp 136-171.
-
(2002)
Targets in Heterocyclic Systems
, vol.6
, pp. 136-171
-
-
Yus, M.1
Foubelo, F.2
-
28
-
-
0037013633
-
On the mechanism of arene-catalyzed lithiation: The role of arene dianions - naphthalene radical anion versus naphthalene dianion
-
Yus, M.; Herrera, R. P.; Guijarro, A. On the mechanism of arene-catalyzed lithiation: the role of arene dianions - naphthalene radical anion versus naphthalene dianion. Chem.-Eur. J., 2002, 8, 2574-2584.
-
(2002)
Chem.-Eur. J
, vol.8
, pp. 2574-2584
-
-
Yus, M.1
Herrera, R.P.2
Guijarro, A.3
-
29
-
-
23244458679
-
Arenecatalyzed lithiation
-
Rapopport, Z.; Marek, I. Eds, Wiley: Chichester, Part 2
-
Yus, M. Arenecatalyzed lithiation; Rapopport, Z.; Marek, I. Eds.; in The Chemistry of Organolithium Compounds; Wiley: Chichester, 2003; Part 2, pp. 647-747.
-
(2003)
The Chemistry of Organolithium Compounds
, pp. 647-747
-
-
Yus, M.1
-
30
-
-
33646944179
-
Organolithiums by reductive lithiation: The catalytic aromatic method versus the use of preformed aromatic radical-anions. Naphthalene can behave as a catalyst or an inhibitor
-
Yang, A.; Butela, H.; Deng, K.; Doubleday, M. D.; Cohen, T. Organolithiums by reductive lithiation: the catalytic aromatic method versus the use of preformed aromatic radical-anions. Naphthalene can behave as a catalyst or an inhibitor. Tetrahedron, 2006, 62, 6526-6535.
-
(2006)
Tetrahedron
, vol.62
, pp. 6526-6535
-
-
Yang, A.1
Butela, H.2
Deng, K.3
Doubleday, M.D.4
Cohen, T.5
-
31
-
-
51949114996
-
Alkali metal reductions of organic molecules: Why mediated electron transfer from lithium is faster than direct reduction
-
Rees, N. V.; Baron, R.; Kershaw, N. M.; Donohoe, T. J.; Compton, R. G. Alkali metal reductions of organic molecules: why mediated electron transfer from lithium is faster than direct reduction. J. Am. Chem. Soc., 2008, 130, 12256-12257.
-
(2008)
J. Am. Chem. Soc
, vol.130
, pp. 12256-12257
-
-
Rees, N.V.1
Baron, R.2
Kershaw, N.M.3
Donohoe, T.J.4
Compton, R.G.5
-
32
-
-
33644570165
-
Addition of alkali metals to the stilbenes
-
J. Addition of alkali metals to the stilbenes. J. Am. Chem. Soc., 1939, 61, 2106-2110.
-
(1939)
J. Am. Chem. Soc
, vol.61
, pp. 2106-2110
-
-
-
33
-
-
33947469174
-
The direct preparation of benzyllithium
-
Gilman, H.; Gorsich, R. D. The direct preparation of benzyllithium. J. Am. Chem. Soc., 1955, 77, 3134-3135.
-
(1955)
J. Am. Chem. Soc
, vol.77
, pp. 3134-3135
-
-
Gilman, H.1
Gorsich, R.D.2
-
34
-
-
37049078449
-
A superior procedure for generation of substituted benzyllithiums from the corresponding chlorides
-
Smith, K.; Hou, D. A superior procedure for generation of substituted benzyllithiums from the corresponding chlorides. J. Chem. Soc., Perkin Trans. 1, 1995, 185-186.
-
(1995)
J. Chem. Soc., Perkin Trans
, vol.1
, pp. 185-186
-
-
Smith, K.1
Hou, D.2
-
36
-
-
0032568036
-
DTBB-catalysed lithiation of chlorinated benzylic chlorides, alcohols, thiols or amines
-
Gómez, C.; Huerta, F. F.; Yus, M. DTBB-catalysed lithiation of chlorinated benzylic chlorides, alcohols, thiols or amines. Tetrahedron, 1998, 54, 1853-1866.
-
(1998)
Tetrahedron
, vol.54
, pp. 1853-1866
-
-
Gómez, C.1
Huerta, F.F.2
Yus, M.3
-
37
-
-
0343742629
-
Di(lithiomethyl)benzenes from di(chloromethyl)benzenes by a DTBB-catalysed lithiation under Barbier-type conditions
-
Gómez, C.; Huerta, F. F.; Yus, M. Di(lithiomethyl)benzenes from di(chloromethyl)benzenes by a DTBB-catalysed lithiation under Barbier-type conditions. Tetrahedron, 1997, 53, 13897-13904.
-
(1997)
Tetrahedron
, vol.53
, pp. 13897-13904
-
-
Gómez, C.1
Huerta, F.F.2
Yus, M.3
-
38
-
-
15444368898
-
DTBB-catalysed lithiation of 2,6-bis(chloromethyl)pyridine
-
Gómez, C.; Maciá, B.; Yus, M. DTBB-catalysed lithiation of 2,6-bis(chloromethyl)pyridine. ARKIVOC, 2005, ix, 10-20.
-
(2005)
ARKIVOC
, Issue.ix
, pp. 10-20
-
-
Gómez, C.1
Maciá, B.2
Yus, M.3
-
39
-
-
0033612118
-
Polymer supported arene-catalysed lithiation reactions
-
Gómez, C.; Ruiz, S.; Yus, M. Polymer supported arene-catalysed lithiation reactions. Tetrahedron, 1999, 55, 7017-7026.
-
(1999)
Tetrahedron
, vol.55
, pp. 7017-7026
-
-
Gómez, C.1
Ruiz, S.2
Yus, M.3
-
40
-
-
6344234802
-
Lithiation reactions catalyzed by linear and cross-linked arene-based polymers. Generation of functionalized organolithium compounds
-
we thank a reviewer for calling our attention on this paper
-
Candela, P.; Gómez, C.; Yus, M. Lithiation reactions catalyzed by linear and cross-linked arene-based polymers. Generation of functionalized organolithium compounds. Rus. J. Org. Chem., 2004, 40, 795-801; we thank a reviewer for calling our attention on this paper.
-
(2004)
Rus. J. Org. Chem
, vol.40
, pp. 795-801
-
-
Candela, P.1
Gómez, C.2
Yus, M.3
-
41
-
-
0037017005
-
ROMPgel-supported biphenyl and naphthalene: Reagents for lithiation reactions with minimal purification
-
Arnauld, T.; Barrett, A. G. M.; Hopkins, B. T. ROMPgel-supported biphenyl and naphthalene: reagents for lithiation reactions with minimal purification. Tetrahedron Lett., 2002, 43, 1081-1083.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 1081-1083
-
-
Arnauld, T.1
Barrett, A.G.M.2
Hopkins, B.T.3
-
42
-
-
0037194298
-
Polyphenylene as an electron transfer catalyst in lithiation processes
-
Yus, M.; Gómez, C.; Candela, P. Polyphenylene as an electron transfer catalyst in lithiation processes. Tetrahedron, 2002, 58, 6207-6210.
-
(2002)
Tetrahedron
, vol.58
, pp. 6207-6210
-
-
Yus, M.1
Gómez, C.2
Candela, P.3
-
43
-
-
0037430443
-
Functionalised linear and cross-linked polystyrenes from chloromethylated polymers through their organolithium derivatives
-
Yus, M.; Gómez, C.; Candela, P. Functionalised linear and cross-linked polystyrenes from chloromethylated polymers through their organolithium derivatives. Tetrahedron, 2003, 59, 1909-1916.
-
(2003)
Tetrahedron
, vol.59
, pp. 1909-1916
-
-
Yus, M.1
Gómez, C.2
Candela, P.3
-
44
-
-
0342452806
-
Reactions of aromatic radical anions. VIII. Organometallic synthesis using sodium naphthalene
-
Bank, S.; Bank, J. F. Reactions of aromatic radical anions. VIII. Organometallic synthesis using sodium naphthalene. Tetrahedron Lett., 1971, 12, 4581-4583.
-
(1971)
Tetrahedron Lett
, vol.12
, pp. 4581-4583
-
-
Bank, S.1
Bank, J.F.2
-
45
-
-
35348918249
-
Polymer supported naphthalene-catalysed sodium reactions
-
van den Ancker, T. R.; Love, C. J. Polymer supported naphthalene-catalysed sodium reactions. Org. Biomol. Chem., 2007, 5, 3520-3523.
-
(2007)
Org. Biomol. Chem
, vol.5
, pp. 3520-3523
-
-
van den Ancker, T.R.1
Love, C.J.2
-
46
-
-
0021969281
-
Antineoplastic agents. 113. Synthesis of natural (-)-combretastatin
-
Pettit, G. R.; Singh, S. B.; Cragg, G. M. Antineoplastic agents. 113. Synthesis of natural (-)-combretastatin. J. Org. Chem., 1985, 50, 3404-3406.
-
(1985)
J. Org. Chem
, vol.50
, pp. 3404-3406
-
-
Pettit, G.R.1
Singh, S.B.2
Cragg, G.M.3
-
47
-
-
0000896657
-
Synthesis of (±)-isocombretastatins A-C
-
Singh, S. B.; Pettit, G. R. Synthesis of (±)-isocombretastatins A-C. Synth. Commun., 1987, 17, 877-892.
-
(1987)
Synth. Commun
, vol.17
, pp. 877-892
-
-
Singh, S.B.1
Pettit, G.R.2
-
48
-
-
0009782132
-
Organic sonochemistry. New ultrasonically accelerated reactions involving lithium
-
For a similar procedure, see
-
For a similar procedure, see: Boudjouk, P.; Sooriyakumaran, R.; Han, B.-H. Organic sonochemistry. New ultrasonically accelerated reactions involving lithium. J. Org. Chem., 1986, 51, 2818-2819.
-
(1986)
J. Org. Chem
, vol.51
, pp. 2818-2819
-
-
Boudjouk, P.1
Sooriyakumaran, R.2
Han, B.-H.3
-
49
-
-
0010983003
-
2-substituierter Benzole in der Gasphase und in Lösung
-
2-substituierter Benzole in der Gasphase und in Lösung. Chem. Ber., 1978, 111, 3552-3572;
-
(1978)
Chem. Ber
, vol.111
, pp. 3552-3572
-
-
Bock, H.1
Kaim, W.2
-
51
-
-
0012985243
-
Generation of allylic and benzylic organolithium compounds by fluorine-lithium exchange: Reaction with electrophiles
-
Guijarro, D.; Yus, M. Generation of allylic and benzylic organolithium compounds by fluorine-lithium exchange: reaction with electrophiles. J. Organomet. Chem., 2001, 624, 53-57.
-
(2001)
J. Organomet. Chem
, vol.624
, pp. 53-57
-
-
Guijarro, D.1
Yus, M.2
-
52
-
-
84956095217
-
Forschungen auf dem Gebiete der alkaliorganischen Verbindungen. V. Versuche mit Triphenylmethyl- und Diphenylmethylnatrium
-
particularly pages 15-21
-
Schlenk, W.; Bergmann, E. Forschungen auf dem Gebiete der alkaliorganischen Verbindungen. V. Versuche mit Triphenylmethyl- und Diphenylmethylnatrium. Justus Liebigs Ann. Chem., 1928, 464, 1-42, particularly pages 15-21.
-
(1928)
Justus Liebigs Ann. Chem
, vol.464
, pp. 1-42
-
-
Schlenk, W.1
Bergmann, E.2
-
53
-
-
0242339231
-
Zur Kenntnis des dreiwertigen Kohlenstoffs: II. Die Umwandlung von Äthern tertiärer Alkohole in organische Kaliumverbindungen und sechsfach substituierte Aethanderivate
-
Ziegler, K.; Schnell, B. Zur Kenntnis des dreiwertigen Kohlenstoffs: II. Die Umwandlung von Äthern tertiärer Alkohole in organische Kaliumverbindungen und sechsfach substituierte Aethanderivate. Justus Liebigs Ann. Chem., 1924, 437, 227-255.
-
(1924)
Justus Liebigs Ann. Chem
, vol.437
, pp. 227-255
-
-
Ziegler, K.1
Schnell, B.2
-
54
-
-
84943086859
-
Metallorganische Verbindungen, XXIII. Über α-Phenyl-Isopropyl-Kalium
-
Ziegler, K.; Dislich, H. Metallorganische Verbindungen, XXIII. Über α-Phenyl-Isopropyl-Kalium. Chem. Ber., 1957, 90, 1107-1115.
-
(1957)
Chem. Ber
, vol.90
, pp. 1107-1115
-
-
Ziegler, K.1
Dislich, H.2
-
55
-
-
0345010864
-
Direct preparation of benzyllithium by cleavage reactions
-
Gilman, H.; McNinch, H. A.; Wittemberg, D. Direct preparation of benzyllithium by cleavage reactions. J. Org. Chem., 1958, 23, 2044-2045.
-
(1958)
J. Org. Chem
, vol.23
, pp. 2044-2045
-
-
Gilman, H.1
McNinch, H.A.2
Wittemberg, D.3
-
56
-
-
9544258461
-
Ortho-substitution of benzyl-type Grignard reagents by cyanogen and thiocyanogen
-
Eastham, J. F.; Cannon, D. Y. Ortho-substitution of benzyl-type Grignard reagents by cyanogen and thiocyanogen. J. Org. Chem., 1960, 25, 1504-1506.
-
(1960)
J. Org. Chem
, vol.25
, pp. 1504-1506
-
-
Eastham, J.F.1
Cannon, D.Y.2
-
57
-
-
0028256007
-
Reductive electrophilic substitution of diarylmethyl methyl ethers: Synthetic applications
-
Azzena, U.; Melloni, G.; Fenude, E.; Finà, C.; Marchetti, M.; Sechi, B. Reductive electrophilic substitution of diarylmethyl methyl ethers: synthetic applications. Synth. Commun., 1994, 24, 591-599.
-
(1994)
Synth. Commun
, vol.24
, pp. 591-599
-
-
Azzena, U.1
Melloni, G.2
Fenude, E.3
Finà, C.4
Marchetti, M.5
Sechi, B.6
-
58
-
-
0029150777
-
Metalation of arylmethyl methyl ethers and connection with their reductive electrophilic substitution
-
Azzena, U.; Demartis, S.; Fiori, M. G.; Melloni, G.; Pisano, L. Metalation of arylmethyl methyl ethers and connection with their reductive electrophilic substitution. Tetrahedron Lett., 1995, 36, 5641-5644.
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 5641-5644
-
-
Azzena, U.1
Demartis, S.2
Fiori, M.G.3
Melloni, G.4
Pisano, L.5
-
59
-
-
0030722262
-
Reductive lithiation of arylalkyl methyl ethers
-
Azzena, U.; Carta, S.; Melloni, G.; Sechi, A. Reductive lithiation of arylalkyl methyl ethers. Tetrahedron, 1997, 53, 16205-16212.
-
(1997)
Tetrahedron
, vol.53
, pp. 16205-16212
-
-
Azzena, U.1
Carta, S.2
Melloni, G.3
Sechi, A.4
-
60
-
-
0742289525
-
Reductive lithiation of alkoxy-substituted benzyl methyl ethers and connection with cross-coupling reactions
-
Azzena, U.; Dettori, G.; Pireddu, R.; Pisano, L. Reductive lithiation of alkoxy-substituted benzyl methyl ethers and connection with cross-coupling reactions. Tetrahedron, 2004, 60, 1617-1623.
-
(2004)
Tetrahedron
, vol.60
, pp. 1617-1623
-
-
Azzena, U.1
Dettori, G.2
Pireddu, R.3
Pisano, L.4
-
61
-
-
0002064932
-
Organoalkali reagents
-
Schlosser, M., Ed, Wiley: Chichester, chapter 1
-
Schlosser, M. Organoalkali reagents; Schlosser, M., Ed.; in Organometallics in Synthesis; Wiley: Chichester, 1994, chapter 1; pp. 1-166.
-
(1994)
Organometallics in Synthesis
, pp. 1-166
-
-
Schlosser, M.1
-
62
-
-
84918616617
-
Fluorine- and trifluoromethyl-substituted toluenes: Site selective metalation of aromatic or benzylic positions
-
and references cited therein
-
Takagishi, S.; Schlosser, M. Fluorine- and trifluoromethyl-substituted toluenes: site selective metalation of aromatic or benzylic positions. Synlett, 1991, 119-121, and references cited therein.
-
(1991)
Synlett
, pp. 119-121
-
-
Takagishi, S.1
Schlosser, M.2
-
63
-
-
0142153186
-
Practical generation of 3,5-dimethoxybenzyllithium: Application to the synthesis of 5- substituted-resorcinols
-
Azzena, U.; Dettori, G.; Idini, M. V.; Pisano, L.; Sechi, G. Practical generation of 3,5-dimethoxybenzyllithium: application to the synthesis of 5- substituted-resorcinols. Appl. Organometal. Chem., 2003, 17, 851-855.
-
(2003)
Appl. Organometal. Chem
, vol.17
, pp. 851-855
-
-
Azzena, U.1
Dettori, G.2
Idini, M.V.3
Pisano, L.4
Sechi, G.5
-
64
-
-
35348866727
-
Ion pairing effects on the regioselectivity of arylic versus benzylic C-O bond reductive cleavage: Synthetic applications
-
Azzena, U.; Dettori, G.; Mascia, I.; Pisano, L.; Pittalis, M. Ion pairing effects on the regioselectivity of arylic versus benzylic C-O bond reductive cleavage: synthetic applications. Tetrahedron, 2007, 63, 11998-12006.
-
(2007)
Tetrahedron
, vol.63
, pp. 11998-12006
-
-
Azzena, U.1
Dettori, G.2
Mascia, I.3
Pisano, L.4
Pittalis, M.5
-
65
-
-
0033577819
-
Synthesis and stereoselective reactions of new stable α-ferrocenyllithium derivatives. An umpolung of the ferrocene reactivity
-
Ireland, T.; Perea, J. J. A.; Knochel, P. Synthesis and stereoselective reactions of new stable α-ferrocenyllithium derivatives. An umpolung of the ferrocene reactivity. Angew. Chem. Int. Ed. 1999, 38, 1457-1460.
-
(1999)
Angew. Chem. Int. Ed
, vol.38
, pp. 1457-1460
-
-
Ireland, T.1
Perea, J.J.A.2
Knochel, P.3
-
66
-
-
0001820427
-
Reductive opening of saturated oxa-, aza- and thia-cycles by means of an arene-promoted lithiation: Synthetic applications
-
Yus, M.; Foubelo, F. Reductive opening of saturated oxa-, aza- and thia-cycles by means of an arene-promoted lithiation: synthetic applications. Rev. Heteroatom Chem., 1997, 17, 73-107.
-
(1997)
Rev. Heteroatom Chem
, vol.17
, pp. 73-107
-
-
Yus, M.1
Foubelo, F.2
-
67
-
-
0141988919
-
Ring opening of heterocycles by an arene-catalyzed lithiation
-
Yus, M. Ring opening of heterocycles by an arene-catalyzed lithiation. Pure Appl. Chem., 2003, 75, 1453-1475.
-
(2003)
Pure Appl. Chem
, vol.75
, pp. 1453-1475
-
-
Yus, M.1
-
68
-
-
33745418080
-
Homologation of heterocycles by a sequential reductive opening lithiation-electrophilic substitution-cyclization
-
Yus, M.; Foubelo, F. Homologation of heterocycles by a sequential reductive opening lithiation-electrophilic substitution-cyclization. Adv. Heterocycl. Chem. 2006, 91, 135-158;
-
(2006)
Adv. Heterocycl. Chem
, vol.91
, pp. 135-158
-
-
Yus, M.1
Foubelo, F.2
-
69
-
-
68349103269
-
Connecting heterocycles via a catalyzed lithiation
-
Foubelo, F.; García, D.; Moreno B.; Yus, M. Connecting heterocycles via a catalyzed lithiation. ARKIVOC, 2009, ix, 183-194.
-
(2009)
ARKIVOC
, vol.ix
, pp. 183-194
-
-
Foubelo, F.1
García, D.2
Moreno, B.3
Yus, M.4
-
70
-
-
33748222999
-
Structures of organo alkali metal complexes and related compounds
-
Weiss, E. Structures of organo alkali metal complexes and related compounds. Angew. Chem. Int. Ed., 1993, 32, 1501-1523.
-
(1993)
Angew. Chem. Int. Ed
, vol.32
, pp. 1501-1523
-
-
Weiss, E.1
-
71
-
-
3242659209
-
Beyond thermodynamic acidity: A perspective on the complex-induced proximity effect (CIPE) in deprotonation reactions
-
Whisler, M. C.; MacNeil, S.; Snieckus, V.; Beak, P. Beyond thermodynamic acidity: a perspective on the complex-induced proximity effect (CIPE) in deprotonation reactions. Angew. Chem. Int. Ed., 2004, 43, 2206-2225.
-
(2004)
Angew. Chem. Int. Ed
, vol.43
, pp. 2206-2225
-
-
Whisler, M.C.1
Macneil, S.2
Snieckus, V.3
Beak, P.4
-
72
-
-
84985566360
-
Organometallic derivatives of epoxides
-
Bartmann, E. Organometallic derivatives of epoxides. Angew. Chem. Int. Ed., 1986, 25, 653-654.
-
(1986)
Angew. Chem. Int. Ed
, vol.25
, pp. 653-654
-
-
Bartmann, E.1
-
73
-
-
15044355001
-
Reductive ring opening of cis- and trans-2,3-diphenyloxirane: A common intermediate
-
Yus, M.; Maciá, B.; Gómez, C.; Soler, T.; Falvello, L. R.; Fanwick, P. E. Reductive ring opening of cis- and trans-2,3-diphenyloxirane: a common intermediate. Tetrahedron, 2005, 61, 3865-3871.
-
(2005)
Tetrahedron
, vol.61
, pp. 3865-3871
-
-
Yus, M.1
Maciá, B.2
Gómez, C.3
Soler, T.4
Falvello, L.R.5
Fanwick, P.E.6
-
74
-
-
0010563860
-
Reaction of oxiranes with lithium: Deoxygenation leading to olefins
-
Gurudutt, K. N.; Ravindranath, B. Reaction of oxiranes with lithium: deoxygenation leading to olefins. Tetrahedron Lett., 1980, 21, 1173-1174.
-
(1980)
Tetrahedron Lett
, vol.21
, pp. 1173-1174
-
-
Gurudutt, K.N.1
Ravindranath, B.2
-
75
-
-
0024850803
-
Y-Lithioalkoxides via reductive lithiation of oxetanes by aromatic radical anions
-
Mudryk, B.; Cohen, T. y-Lithioalkoxides via reductive lithiation of oxetanes by aromatic radical anions. J. Org. Chem., 1989, 54, 5657-5659.
-
(1989)
J. Org. Chem
, vol.54
, pp. 5657-5659
-
-
Mudryk, B.1
Cohen, T.2
-
76
-
-
0034681874
-
Reductive cleavage of 2- methyleneoxetanes with lithium and 4,4'-di-tert-butylbiphenyl
-
Hashemzadeh, M.; Howell, A. R. Reductive cleavage of 2- methyleneoxetanes with lithium and 4,4'-di-tert-butylbiphenyl. Tetrahedron Lett., 2000, 41, 1855-1858.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 1855-1858
-
-
Hashemzadeh, M.1
Howell, A.R.2
-
77
-
-
0028947968
-
1,2-Di(lithiomethyl)benzene from phthalan: Sequential introduction of two different electrophiles
-
Almena, J.; Foubelo, F.; Yus, M. 1,2-Di(lithiomethyl)benzene from phthalan: sequential introduction of two different electrophiles. Tetrahedron, 1995, 51, 3351-3364.
-
(1995)
Tetrahedron
, vol.51
, pp. 3351-3364
-
-
Almena, J.1
Foubelo, F.2
Yus, M.3
-
78
-
-
0028860818
-
Reductive electrophilic substitution of phthalans and ring expansion to isochroman derivatives
-
Azzena, U.; Demartis, S.; Fiori, M. G.; Melloni, G.; Pisano, L. Reductive electrophilic substitution of phthalans and ring expansion to isochroman derivatives. Tetrahedron Lett. 1995, 36, 8123-8126;
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 8123-8126
-
-
Azzena, U.1
Demartis, S.2
Fiori, M.G.3
Melloni, G.4
Pisano, L.5
-
79
-
-
0000654428
-
Electron-transfer-induced reductive cleavage of phthalans: Reactivity and synthetic applications
-
Azzena, U.; Demartis, S.; Melloni, G. Electron-transfer-induced reductive cleavage of phthalans: reactivity and synthetic applications. J. Org. Chem., 1996, 61, 4913-4919.
-
(1996)
J. Org. Chem
, vol.61
, pp. 4913-4919
-
-
Azzena, U.1
Demartis, S.2
Melloni, G.3
-
80
-
-
2542447275
-
Reductive ring opening of oxygencontaining benzo-fused heterocycles by an arene-catalysed lithiation
-
Yus, M.; Moreno, B.; Foubelo, F. Reductive ring opening of oxygencontaining benzo-fused heterocycles by an arene-catalysed lithiation. Synthesis, 2004, 7, 1115-1118.
-
(2004)
Synthesis
, vol.7
, pp. 1115-1118
-
-
Yus, M.1
Moreno, B.2
Foubelo, F.3
-
81
-
-
0035796512
-
Lewis acid-promoted conjugate addition of functionalised organolithium compounds to electrophilic olefins
-
Yus, M.; Pastor, I. M.; Gomis, J. Lewis acid-promoted conjugate addition of functionalised organolithium compounds to electrophilic olefins. Tetrahedron, 2001, 57, 5799-5805.
-
(2001)
Tetrahedron
, vol.57
, pp. 5799-5805
-
-
Yus, M.1
Pastor, I.M.2
Gomis, J.3
-
82
-
-
0038170220
-
ZnBr2/CuCN-Promoted, highly regioselective SN2 reactions of some functionalised organolithium compounds with allylic and propargylic halides
-
Yus, M.; Gomis, J. ZnBr2/CuCN-Promoted, highly regioselective SN2 reactions of some functionalised organolithium compounds with allylic and propargylic halides. Eur. J. Org. Chem. 2003, 2043-2048;
-
(2003)
Eur. J. Org. Chem
, pp. 2043-2048
-
-
Yus, M.1
Gomis, J.2
-
83
-
-
0035855301
-
Negishi ross-coupling with functionalised organozinc compounds prepared by lithium-zinc transmetallation
-
Yus, M.; Gomis, J. Negishi ross-coupling with functionalised organozinc compounds prepared by lithium-zinc transmetallation. Tetrahedron Lett. 2001, 42, 5721-5724.
-
(2001)
Tetrahedron Lett
, vol.42
, pp. 5721-5724
-
-
Yus, M.1
Gomis, J.2
-
84
-
-
0036087846
-
Palladium-promoted arylation of functionalized organolithium compounds via their zinc derivatives
-
Yus, M.; Gomis, J. Palladium-promoted arylation of functionalized organolithium compounds via their zinc derivatives. Eur. J. Org. Chem. 2002, 1989-1995.
-
(2002)
Eur. J. Org. Chem
, pp. 1989-1995
-
-
Yus, M.1
Gomis, J.2
-
85
-
-
0034603432
-
Copper(I) or (II)-mediated conjugate addition or dimerisation of functionalised organolithium compounds
-
Pastor, I. M.; Yus, M. Copper(I) or (II)-mediated conjugate addition or dimerisation of functionalised organolithium compounds. Tetrahedron Lett. 2000, 41, 1589-1592.
-
(2000)
Tetrahedron Lett
, vol.41
, pp. 1589-1592
-
-
Pastor, I.M.1
Yus, M.2
-
86
-
-
0035901357
-
New reactivity of functionalized organolithium compounds in the presence of Cu(I) or Cu(II) salts: Conjugate addition, acylation or dimerisation
-
Pastor, I. M.; Yus, M. New reactivity of functionalized organolithium compounds in the presence of Cu(I) or Cu(II) salts: conjugate addition, acylation or dimerisation. Tetrahedron 2001, 57, 2371-2378.
-
(2001)
Tetrahedron
, vol.57
, pp. 2371-2378
-
-
Pastor, I.M.1
Yus, M.2
-
87
-
-
67649372526
-
Stereoselective synthesis of 3-substituted tetrahydroisoquinolines from phthalan and chiral N-sulfinylimines
-
García, D.; Moreno, B.; Soler, T.; Foubelo, F.; Yus, M. Stereoselective synthesis of 3-substituted tetrahydroisoquinolines from phthalan and chiral N-sulfinylimines. Tetrahedron Lett., 2009, 50, 4710-4713.
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 4710-4713
-
-
García, D.1
Moreno, B.2
Soler, T.3
Foubelo, F.4
Yus, M.5
-
88
-
-
34147153184
-
Regiochemistry in the reductive opening of phthalan derivatives
-
Foubelo, F.; García, D.; Moreno, B.; Yus, M. Regiochemistry in the reductive opening of phthalan derivatives. Tetrahedron Lett., 2007, 48, 3379-3383.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 3379-3383
-
-
Foubelo, F.1
García, D.2
Moreno, B.3
Yus, M.4
-
89
-
-
0028963397
-
Lithium 2-(2-lithiomethylphenyl)ethanolate from isochroman: Easy preparation of substituted benzoxepines and functionalized arenes
-
Almena, J.; Foubelo, F.; Yus, M. Lithium 2-(2-lithiomethylphenyl)ethanolate from isochroman: easy preparation of substituted benzoxepines and functionalized arenes. Tetrahedron, 1995, 51, 3365-3374.
-
(1995)
Tetrahedron
, vol.51
, pp. 3365-3374
-
-
Almena, J.1
Foubelo, F.2
Yus, M.3
-
90
-
-
0034644622
-
Reductive cleavage of benzannelated cyclic ethers and amines: Synthetic applications
-
Azzena, U.; Demartis, S.; Pilo, L.; Piras, E. Reductive cleavage of benzannelated cyclic ethers and amines: synthetic applications. Tetrahedron, 2000, 56, 8375-8382.
-
(2000)
Tetrahedron
, vol.56
, pp. 8375-8382
-
-
Azzena, U.1
Demartis, S.2
Pilo, L.3
Piras, E.4
-
91
-
-
2142707161
-
Reductive opening of 1H, 3Hbenzo[de]isochromene: Synthesis of 1,8-difunctionalised naphthalenes
-
Foubelo, F.; Moreno, B.; Yus, M. Reductive opening of 1H, 3Hbenzo[de]isochromene: synthesis of 1,8-difunctionalised naphthalenes. Tetrahedron 2004, 60, 4655-4662.
-
(2004)
Tetrahedron
, vol.60
, pp. 4655-4662
-
-
Foubelo, F.1
Moreno, B.2
Yus, M.3
-
92
-
-
8644230797
-
Reductive opening of 2,7- dihydrodinaphthoxepine and thiepine: Easy regioselective preparation of 2,2'- difunctionalised binaphthyls
-
Foubelo, F.; Moreno, B.; Yus, M. Reductive opening of 2,7- dihydrodinaphthoxepine and thiepine: easy regioselective preparation of 2,2'- difunctionalised binaphthyls. Tetrahedron Lett. 2004, 45, 8983-8986.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 8983-8986
-
-
Foubelo, F.1
Moreno, B.2
Yus, M.3
-
93
-
-
23944471332
-
Reductive ring opening of dihydrodibenzothiepine and dihydrodinaphtho-oxepine and -thiepine
-
Foubelo, F.; Moreno, B.; Soler, T.; Yus, M. Reductive ring opening of dihydrodibenzothiepine and dihydrodinaphtho-oxepine and -thiepine. Tetrahedron 2005, 61, 9082-9096.
-
(2005)
Tetrahedron
, vol.61
, pp. 9082-9096
-
-
Foubelo, F.1
Moreno, B.2
Soler, T.3
Yus, M.4
-
94
-
-
0027374658
-
Reductive opening of 2-phenyl-1,3-dioxolanes by a naphthalene-catalysed lithiation: Synthetic applications
-
Gil, J. F.; Ramón, D. J.; Yus, M. Reductive opening of 2-phenyl-1,3-dioxolanes by a naphthalene-catalysed lithiation: synthetic applications. Tetrahedron, 1993, 49, 9535-9546.
-
(1993)
Tetrahedron
, vol.49
, pp. 9535-9546
-
-
Gil, J.F.1
Ramón, D.J.2
Yus, M.3
-
95
-
-
0028111136
-
Single and double reductive cleavage of C-O bonds of aromatic dimethyl acetals and ketals: Generation of benzylic mono- and dicarbanions
-
Azzena, U.; Melloni, G.; Pisano, L.; Sechi, B. Single and double reductive cleavage of C-O bonds of aromatic dimethyl acetals and ketals: generation of benzylic mono- and dicarbanions. Tetrahedron Lett., 1994, 35, 6759-6762.
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 6759-6762
-
-
Azzena, U.1
Melloni, G.2
Pisano, L.3
Sechi, B.4
-
96
-
-
0001889770
-
Reductive lithiation of (arene)tricarbonylchromium acetals
-
Siwek, M. J.; Green, J. R. Reductive lithiation of (arene)tricarbonylchromium acetals. Synlett, 1996, 560-562.
-
(1996)
Synlett
, pp. 560-562
-
-
Siwek, M.J.1
Green, J.R.2
-
97
-
-
0036857656
-
Highly chemoselective lithium metal reductions of benzaldehyde bis(2-methoxyethyl) acetal
-
von Schrader, T.; Woodward, S. Highly chemoselective lithium metal reductions of benzaldehyde bis(2-methoxyethyl) acetal. Eur. J. Org. Chem., 2002, 3833-3836.
-
(2002)
Eur. J. Org. Chem
, pp. 3833-3836
-
-
von Schrader, T.1
Woodward, S.2
-
98
-
-
0033605834
-
Naphthalene-catalysed lithiation of 2-(chlorophenyl)-1,3-dioxolanes: Generation of formyl- and acetylphenyllithium equivalents
-
Huerta, F. F.; Gómez, C.; Yus, M. Naphthalene-catalysed lithiation of 2-(chlorophenyl)-1,3-dioxolanes: generation of formyl- and acetylphenyllithium equivalents. Tetrahedron, 1999, 55, 4043-4050.
-
(1999)
Tetrahedron
, vol.55
, pp. 4043-4050
-
-
Huerta, F.F.1
Gómez, C.2
Yus, M.3
-
99
-
-
30844447201
-
Regioselectivity in arene-catalyzed reductive lithiation of acetals of chlorobenzaldehydes
-
Azzena, U.; Dettori, G.; Sforazzini, G.; Yus, M.; Foubelo, F. Regioselectivity in arene-catalyzed reductive lithiation of acetals of chlorobenzaldehydes. Tetrahedron, 2006, 62, 1557-1563.
-
(2006)
Tetrahedron
, vol.62
, pp. 1557-1563
-
-
Azzena, U.1
Dettori, G.2
Sforazzini, G.3
Yus, M.4
Foubelo, F.5
-
101
-
-
14844321628
-
Reductive lithiation of 1,3-dimethyl-2-arylimidazolidines
-
Azzena, U.; Dettori, G.; Pisano, L.; Siotto, I. Reductive lithiation of 1,3-dimethyl-2-arylimidazolidines. Tetrahedron, 2005, 61, 3177-3182.
-
(2005)
Tetrahedron
, vol.61
, pp. 3177-3182
-
-
Azzena, U.1
Dettori, G.2
Pisano, L.3
Siotto, I.4
-
102
-
-
0034595809
-
Generation and reactivity of α-aminosubstituted arylmethyllithium organometallics
-
Azzena, U.; Pilo, L.; Piras, E. Generation and reactivity of α-aminosubstituted arylmethyllithium organometallics. Tetrahedron, 2000, 56, 3775-3780.
-
(2000)
Tetrahedron
, vol.56
, pp. 3775-3780
-
-
Azzena, U.1
Pilo, L.2
Piras, E.3
-
103
-
-
0027771656
-
Reductive cleavage of N-substituted 2- aryl-1,3-oxazolidines: Generation of α-amino-substituted carbanions
-
Azzena, U.; Melloni, G.; Nigra, C. Reductive cleavage of N-substituted 2- aryl-1,3-oxazolidines: generation of α-amino-substituted carbanions. J. Org. Chem., 1993, 58, 6707-6711.
-
(1993)
J. Org. Chem
, vol.58
, pp. 6707-6711
-
-
Azzena, U.1
Melloni, G.2
Nigra, C.3
-
104
-
-
0036007711
-
Diastereoselective electrophilic substitution of α-aminosubstituted benzylic organometallics
-
Azzena, U. Diastereoselective electrophilic substitution of α-aminosubstituted benzylic organometallics. J. Chem. Soc., Perkin Trans. 1, 2002, 360-365.
-
(2002)
J. Chem. Soc., Perkin Trans
, vol.1
, pp. 360-365
-
-
Azzena, U.1
-
105
-
-
0030834995
-
New homologation of 2-hydroxy and 2-mercapto benzylic alcohols
-
Choudhury, P. K.; Almena, J.; Foubelo, F.; Yus, M. New homologation of 2-hydroxy and 2-mercapto benzylic alcohols. Tetrahedron, 1997, 53, 17373-17382.
-
(1997)
Tetrahedron
, vol.53
, pp. 17373-17382
-
-
Choudhury, P.K.1
Almena, J.2
Foubelo, F.3
Yus, M.4
-
106
-
-
0032949502
-
Generation of γ-oxy-substituted benzylithium derivatives by reductive lithiation of 4-phenyl-1,3-dioxanes
-
Azzena, U.; Pilo, L. Generation of γ-oxy-substituted benzylithium derivatives by reductive lithiation of 4-phenyl-1,3-dioxanes. Synthesis, 1999, 664-668.
-
(1999)
Synthesis
, pp. 664-668
-
-
Azzena, U.1
Pilo, L.2
-
107
-
-
0037100145
-
Diastereoselective electrophilic substitution of γ-oxy-substituted benzyllithiums
-
Arrica, M. A.; Azzena, U.; Pilo, L.; Piras, E. Diastereoselective electrophilic substitution of γ-oxy-substituted benzyllithiums. Tetrahedron Lett., 2002, 43, 5137-5139.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 5137-5139
-
-
Arrica, M.A.1
Azzena, U.2
Pilo, L.3
Piras, E.4
-
108
-
-
0029097618
-
Direct transformation of allylic and benzylic alcohols or their silylated derivatives into organolithium compounds
-
Alonso, E.; Guijarro, D.; Yus, M. Direct transformation of allylic and benzylic alcohols or their silylated derivatives into organolithium compounds. Tetrahedron, 1995, 51, 11457-11464.
-
(1995)
Tetrahedron
, vol.51
, pp. 11457-11464
-
-
Alonso, E.1
Guijarro, D.2
Yus, M.3
-
109
-
-
0037471514
-
Preparation of α,n-dilithiotoluene equivalents. Synthesis of tamoxifen
-
Yus, M.; Ramón, D. J.; Gómez, I. Preparation of α,n-dilithiotoluene equivalents. Synthesis of tamoxifen. Tetrahedron, 2003, 59, 3219-3225.
-
(2003)
Tetrahedron
, vol.59
, pp. 3219-3225
-
-
Yus, M.1
Ramón, D.J.2
Gómez, I.3
-
110
-
-
0031053263
-
Simple synthesis of 5-substituted resorcinols: A revisited family of interesting bioactive molecules
-
Alonso, E.; Ramón, D. J.; Yus, M. Simple synthesis of 5-substituted resorcinols: a revisited family of interesting bioactive molecules. J. Org. Chem., 1997, 62, 417-421.
-
(1997)
J. Org. Chem
, vol.62
, pp. 417-421
-
-
Alonso, E.1
Ramón, D.J.2
Yus, M.3
-
111
-
-
0033520272
-
Generation of allylic and benzylic organolithium reagents from the corresponding ester, amide, carbonate, carbamate and urea derivatives
-
Alonso, E.; Guijarro, D.; Martínez, P.; Ramón, D. J.; Yus, M. Generation of allylic and benzylic organolithium reagents from the corresponding ester, amide, carbonate, carbamate and urea derivatives. Tetrahedron, 1999, 55, 11027-11038.
-
(1999)
Tetrahedron
, vol.55
, pp. 11027-11038
-
-
Alonso, E.1
Guijarro, D.2
Martínez, P.3
Ramón, D.J.4
Yus, M.5
-
112
-
-
0026633731
-
Naphthalene-catalysed lithiation of allylic and benzylic mesylates: A new method for allyl, methallyl, and benzyl lithium
-
Guijarro, D.; Mancheño, B.; Yus, M. Naphthalene-catalysed lithiation of allylic and benzylic mesylates: a new method for allyl, methallyl, and benzyl lithium. Tetrahedron, 1992, 48, 4593-4600.
-
(1992)
Tetrahedron
, vol.48
, pp. 4593-4600
-
-
Guijarro, D.1
Mancheño, B.2
Yus, M.3
-
113
-
-
0028292037
-
Direct transformation of trialkyl phosphates into organolithium compounds by a DTBB-catalysed lithiation
-
Guijarro, D.; Mancheño, B.; Yus, M. Direct transformation of trialkyl phosphates into organolithium compounds by a DTBB-catalysed lithiation. Tetrahedron, 1994, 50, 8551-8558.
-
(1994)
Tetrahedron
, vol.50
, pp. 8551-8558
-
-
Guijarro, D.1
Mancheño, B.2
Yus, M.3
-
114
-
-
3242793478
-
Electron-transfer-induced reductive dealkoxylation of alkyl aryl ethers. III. Reductive cleavage of methoxy-substituted N,Ndimethylanilines (N,N-dimethylanisidines)
-
Azzena, U.; Dessanti, F.; Melloni, G.; Pisano, L. Electron-transfer-induced reductive dealkoxylation of alkyl aryl ethers. III. Reductive cleavage of methoxy-substituted N,Ndimethylanilines (N,N-dimethylanisidines). ARKIVOC, 2002, v, 181-188.
-
(2002)
ARKIVOC
, vol.v
, pp. 181-188
-
-
Azzena, U.1
Dessanti, F.2
Melloni, G.3
Pisano, L.4
-
115
-
-
2942668485
-
Benzyllithium from methylated benzylamine and its ammonium salt via naphthalene-catalyzed carbonnitrogen bond reductive cleavage
-
Guijarro, D.; Martinez, P. J.; Nájera, C.; Yus, M. Benzyllithium from methylated benzylamine and its ammonium salt via naphthalene-catalyzed carbonnitrogen bond reductive cleavage. ARKIVOC, 2004, iv, 5-13.
-
(2004)
ARKIVOC
, vol.iv
, pp. 5-13
-
-
Guijarro, D.1
Martinez, P.J.2
Nájera, C.3
Yus, M.4
-
116
-
-
0001453330
-
N,2-dilithioalkylamines from aziridines by naphthalene-catalyzed reductive opening. synthetic applications
-
Almena, J.; Foubelo, F.; Yus, M. N,2-dilithioalkylamines from aziridines by naphthalene-catalyzed reductive opening. synthetic applications. J. Org. Chem., 1994, 59, 3210-3215.
-
(1994)
J. Org. Chem
, vol.59
, pp. 3210-3215
-
-
Almena, J.1
Foubelo, F.2
Yus, M.3
-
117
-
-
0028240601
-
4,4'-Di-tert-butylbiphenyl-catalysed reductive opening of azetidines with lithium: A direct preparation of 3,Ndilithioalkylamines
-
Almena, J.; Foubelo, F.; Yus, M. 4,4'-Di-tert-butylbiphenyl-catalysed reductive opening of azetidines with lithium: a direct preparation of 3,Ndilithioalkylamines. Tetrahedron, 1994, 50, 5775-5782.
-
(1994)
Tetrahedron
, vol.50
, pp. 5775-5782
-
-
Almena, J.1
Foubelo, F.2
Yus, M.3
-
118
-
-
0029936158
-
Nitrogen-containing remote functionalized organolithium compounds by reductive opening of five- and six-membered heterocycles
-
Almena, J.; Foubelo, F.; Yus, M. Nitrogen-containing remote functionalized organolithium compounds by reductive opening of five- and six-membered heterocycles. Tetrahedron, 1996, 52, 8545-8564.
-
(1996)
Tetrahedron
, vol.52
, pp. 8545-8564
-
-
Almena, J.1
Foubelo, F.2
Yus, M.3
-
119
-
-
0026101466
-
Benzotriazole: A novel synthetic auxiliary
-
Katritzky, A. R.; Rachwal, S.; Hitchings, G. J. Benzotriazole: a novel synthetic auxiliary. Tetrahedron, 1991, 47, 2683-2732.
-
(1991)
Tetrahedron
, vol.47
, pp. 2683-2732
-
-
Katritzky, A.R.1
Rachwal, S.2
Hitchings, G.J.3
-
120
-
-
0028336928
-
Benzotriazole as a synthetic auxiliary: Benzotriazolylalkylations and benzotriazole-mediated heteroalkylation
-
Katritzky, A. R.; Lan, X., Fan, W.-Q. Benzotriazole as a synthetic auxiliary: benzotriazolylalkylations and benzotriazole-mediated heteroalkylation. Synthesis, 1994, 445-456.
-
(1994)
Synthesis
, pp. 445-456
-
-
Katritzky, A.R.1
Lan, X.2
Fan, W.-Q.3
-
121
-
-
0000269990
-
Benzotriazole-mediated arylalkylation and heteroarylalkylation
-
Katritzky, A. R.; Lan, X. Benzotriazole-mediated arylalkylation and heteroarylalkylation. Chem. Soc. Rev., 1994, 363-373.
-
(1994)
Chem. Soc. Rev
, pp. 363-373
-
-
Katritzky, A.R.1
Lan, X.2
-
122
-
-
0000537071
-
Transformations of N-substituted benzotriazoles into the corresponding carbanions by C-benzotriazole bond scission
-
Katritzky, A. R.; Qi, M. Transformations of N-substituted benzotriazoles into the corresponding carbanions by C-benzotriazole bond scission. J. Org. Chem., 1997, 62, 4116-4120.
-
(1997)
J. Org. Chem
, vol.62
, pp. 4116-4120
-
-
Katritzky, A.R.1
Qi, M.2
-
123
-
-
0032537071
-
1,1-Bis(benzotriazolyl) derivatives as gem-dianion synthons
-
Katritzky, A. R.; Fali, C. N.; Qi, M. 1,1-Bis(benzotriazolyl) derivatives as gem-dianion synthons. Tetrahedron Lett., 1998, 39, 2289-2292.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 2289-2292
-
-
Katritzky, A.R.1
Fali, C.N.2
Qi, M.3
-
124
-
-
0001858130
-
Benzotriazole - stabilized carbanions: Generation, reactivity, and synthetic utility
-
Katritzky, A. R.; Yang, Z.; Cundy, D. J. Benzotriazole - stabilized carbanions: generation, reactivity, and synthetic utility. Aldrichim. Acta, 1994, 27, 31-38.
-
(1994)
Aldrichim. Acta
, vol.27
, pp. 31-38
-
-
Katritzky, A.R.1
Yang, Z.2
Cundy, D.J.3
-
125
-
-
0030569283
-
Arene-catalysed lithiation of triflates and triflamides under Barbier-type conditions: An indirect transformation of alcohols and amines into organolithium compounds
-
Alonso, E.; Ramón, D. J.; Yus, M. Arene-catalysed lithiation of triflates and triflamides under Barbier-type conditions: an indirect transformation of alcohols and amines into organolithium compounds. Tetrahedron, 1996, 52, 14341-14348.
-
(1996)
Tetrahedron
, vol.52
, pp. 14341-14348
-
-
Alonso, E.1
Ramón, D.J.2
Yus, M.3
-
126
-
-
84982446988
-
Tris-phenylmercapto-methyllithium ein ungewöhnliches Carbenoid
-
Seebach, D. Tris-phenylmercapto-methyllithium ein ungewöhnliches Carbenoid. Chem. Ber., 1972, 105, 487-510.
-
(1972)
Chem. Ber
, vol.105
, pp. 487-510
-
-
Seebach, D.1
-
127
-
-
85196230916
-
-
8
-
8.
-
-
-
-
128
-
-
0038166703
-
Reductive lithiation of alkyl phenyl sulfides in diethyl ether. A ready access to α,α-dialkylbenzyllithiums
-
Screttas, C. G.; Heropoulos, G. A.; Micha-Screttas, M.; Steele, B. R.; Catsoulacos, D. P. Reductive lithiation of alkyl phenyl sulfides in diethyl ether. A ready access to α,α-dialkylbenzyllithiums. Tetrahedron Lett., 2003, 44, 5633-5635.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 5633-5635
-
-
Screttas, C.G.1
Heropoulos, G.A.2
Micha-Screttas, M.3
Steele, B.R.4
Catsoulacos, D.P.5
-
129
-
-
0001739154
-
Hydrocarbon-soluble organoalkali-metal reagents. Preparation of aryl derivatives
-
2 as an additive in organometallic chemistry, see
-
2 as an additive in organometallic chemistry, see: Screttas, C. G.; Micha-Screttas, M. Hydrocarbon-soluble organoalkali-metal reagents. Preparation of aryl derivatives. Organometallics, 1984, 3, 904-907;
-
(1984)
Organometallics
, vol.3
, pp. 904-907
-
-
Screttas, C.G.1
Micha-Screttas, M.2
-
130
-
-
0001566556
-
Metal alkoxide modified organometallic reagents. Preparation and stability of organolithium reagents in tetrahydrofuran in the presence of magnesium 2-ethoxyethoxide
-
Screttas, C. G.; Steele B. R. Metal alkoxide modified organometallic reagents. Preparation and stability of organolithium reagents in tetrahydrofuran in the presence of magnesium 2-ethoxyethoxide. J. Org. Chem., 1989, 54, 1013-1017.
-
(1989)
J. Org. Chem
, vol.54
, pp. 1013-1017
-
-
Screttas, C.G.1
Steele, B.R.2
-
131
-
-
0034654109
-
Chemoselective catalytic sidechain alkylation of aromatics by ethylene leading to sterically demanding alkylbenzenes
-
Steele, B. R.; Screttas, C. G. Chemoselective catalytic sidechain alkylation of aromatics by ethylene leading to sterically demanding alkylbenzenes. J. Am. Chem. Soc., 2000, 122, 2391-2392.
-
(2000)
J. Am. Chem. Soc
, vol.122
, pp. 2391-2392
-
-
Steele, B.R.1
Screttas, C.G.2
-
132
-
-
0036045428
-
Applications of novel sterically demanding aromatics in organometallic synthesis
-
Steele, B. R.; Micha-Screttas, M.; Screttas, C. G. Applications of novel sterically demanding aromatics in organometallic synthesis. Appl. Organometal. Chem., 2002, 16, 501-505.
-
(2002)
Appl. Organometal. Chem
, vol.16
, pp. 501-505
-
-
Steele, B.R.1
Micha-Screttas, M.2
Screttas, C.G.3
-
133
-
-
0002974335
-
The Peterson olefination reaction
-
For a review on the Peterson olefination reaction, see:, Paquette, L.A., Ed, John Wiley: New York
-
For a review on the Peterson olefination reaction, see: Ager, D.J. The Peterson olefination reaction. Paquette, L.A., Ed.; in Org. React.; John Wiley: New York, 1990, Vol. 38, pp. 1-223.
-
(1990)
Org. React
, vol.38
, pp. 1-223
-
-
Ager, D.J.1
-
134
-
-
0001727276
-
A general procedure for preparing α-lithiosilanes. Generalization of the Peterson olefination
-
Cohen, T.; Sherbine, J. P.; Matz, J. R.; Hutchins, R. R.; McHenry, B. M.; Willey, P. R. A general procedure for preparing α-lithiosilanes. Generalization of the Peterson olefination. J. Am. Chem. Soc., 1984, 106, 3245-3252.
-
(1984)
J. Am. Chem. Soc
, vol.106
, pp. 3245-3252
-
-
Cohen, T.1
Sherbine, J.P.2
Matz, J.R.3
Hutchins, R.R.4
McHenry, B.M.5
Willey, P.R.6
-
135
-
-
37049076676
-
Synthesis of alkenes via the Peterson reaction
-
D. J. Synthesis of alkenes via the Peterson reaction. J. Chem. Soc., Perkin Trans. 1, 1986, 183-194.
-
(1986)
J. Chem. Soc., Perkin Trans
, vol.1
, pp. 183-194
-
-
-
136
-
-
37049069404
-
The synthesis of ketones via α-silyl sulphides
-
Ager, D. J. The synthesis of ketones via α-silyl sulphides. J. Chem. Soc., Perkin Trans. 1, 1986, 195-204.
-
(1986)
J. Chem. Soc., Perkin Trans
, vol.1
, pp. 195-204
-
-
Ager, D.J.1
-
137
-
-
0000243198
-
The synthesis and some applications of new 1,3-dilithiopropanes: Dimethylbis(α-lithiobenzyl)silane and its germanium analogue
-
Akkerman, O. S.; Bickelhaupt, F. The synthesis and some applications of new 1,3-dilithiopropanes: dimethylbis(α-lithiobenzyl)silane and its germanium analogue. J. Organomet. Chem., 1988, 338, 159-168.
-
(1988)
J. Organomet. Chem
, vol.338
, pp. 159-168
-
-
Akkerman, O.S.1
Bickelhaupt, F.2
-
138
-
-
0027999898
-
Enantioselective synthesis of γ-hydroxysilanes, 1,3- diols and cyclopropanes by reaction of a chiral epoxide with a racemic α-silyl organolithium reagent
-
Corey, E. J.; Chen, Z. Enantioselective synthesis of γ-hydroxysilanes, 1,3- diols and cyclopropanes by reaction of a chiral epoxide with a racemic α-silyl organolithium reagent. Tetrahedron Lett., 1994, 35, 8731-8734.
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 8731-8734
-
-
Corey, E.J.1
Chen, Z.2
-
139
-
-
0038691529
-
Direct transformation of allylic and benzylic thiols, thioethers, and disulfides into organolithium compounds
-
Yus, M.; Martínez, P.; Guijarro, D. Direct transformation of allylic and benzylic thiols, thioethers, and disulfides into organolithium compounds. Synth. Commun., 2003, 33, 2365-2376.
-
(2003)
Synth. Commun
, vol.33
, pp. 2365-2376
-
-
Yus, M.1
Martínez, P.2
Guijarro, D.3
-
140
-
-
0030937729
-
Reductive opening of phenyl substituted thiacycloalkanes: New way for sulphur-containing organolithium compounds
-
Almena, J., Foubelo, F.; Yus, M. Reductive opening of phenyl substituted thiacycloalkanes: new way for sulphur-containing organolithium compounds. Tetrahedron, 1997, 53, 5563-5572.
-
(1997)
Tetrahedron
, vol.53
, pp. 5563-5572
-
-
Almena, J.1
Foubelo, F.2
Yus, M.3
-
141
-
-
0001262307
-
Reductive opening of thiophthalan: A new route to functionalized sulfur-containing compounds
-
Almena, J.; Foubelo, F.; Yus, M. Reductive opening of thiophthalan: a new route to functionalized sulfur-containing compounds. J. Org. Chem., 1996, 61, 1859-1862.
-
(1996)
J. Org. Chem
, vol.61
, pp. 1859-1862
-
-
Almena, J.1
Foubelo, F.2
Yus, M.3
-
142
-
-
23944471332
-
Reductive ring opening of dihydrodibenzothiepine and dihydrodinaphtho-oxepine and -thiepine
-
Foubelo, F.; Moreno, B.; Soler, T.; Yus, M. Reductive ring opening of dihydrodibenzothiepine and dihydrodinaphtho-oxepine and -thiepine. Tetrahedron, 2005, 61, 9082-9096.
-
(2005)
Tetrahedron
, vol.61
, pp. 9082-9096
-
-
Foubelo, F.1
Moreno, B.2
Soler, T.3
Yus, M.4
-
143
-
-
0028245662
-
Naphthalene-catalysed reductive desulfonylation with lithium: Alkyllithiums from alkyl phenyl sulfones
-
Guijarro, D.; Yus, M. Naphthalene-catalysed reductive desulfonylation with lithium: alkyllithiums from alkyl phenyl sulfones. Tetrahedron Lett., 1994, 35, 2965-2968.
-
(1994)
Tetrahedron Lett
, vol.35
, pp. 2965-2968
-
-
Guijarro, D.1
Yus, M.2
-
144
-
-
0028928103
-
Arene-catalysed reductive desulfonylation and desulfinylation reactions: New routes for alkyllithiums
-
Alonso, E.; Guijarro, D.; Yus, M. Arene-catalysed reductive desulfonylation and desulfinylation reactions: new routes for alkyllithiums. Tetrahedron, 1995, 51, 2699-2708.
-
(1995)
Tetrahedron
, vol.51
, pp. 2699-2708
-
-
Alonso, E.1
Guijarro, D.2
Yus, M.3
-
145
-
-
84918248116
-
Forschungen auf dem Gebiete der alkaliorganischen Verbindungen. I. Über Produkte der Addition von Alkalimetal an mehrfache Kohlenstoff-Kohlenstoff-Bindungen
-
Schlenk, W.; Bergmann, E. Forschungen auf dem Gebiete der alkaliorganischen Verbindungen. I. Über Produkte der Addition von Alkalimetal an mehrfache Kohlenstoff-Kohlenstoff-Bindungen. Justus Liebigs Annalen der Chemie, 1928, 463, 1-97.
-
(1928)
Justus Liebigs Annalen Der Chemie
, vol.463
, pp. 1-97
-
-
Schlenk, W.1
Bergmann, E.2
-
146
-
-
0011132881
-
Living polymers
-
Szwarc, M. Living polymers. Nature, 1956, 178, 1168-1169.
-
(1956)
Nature
, vol.178
, pp. 1168-1169
-
-
Szwarc, M.1
-
147
-
-
33947460098
-
Polymerization initiated by electron transfer to monomer. a new method of formation of block polymers
-
Szwarc, M.; Levy, M.; Milkovich, R. Polymerization initiated by electron transfer to monomer. a new method of formation of block polymers. J. Am. Chem. Soc., 1956, 78, 2656-2657.
-
(1956)
J. Am. Chem. Soc
, vol.78
, pp. 2656-2657
-
-
Szwarc, M.1
Levy, M.2
Milkovich, R.3
-
148
-
-
0000130975
-
A new synthesis of dibasic acids. II. 2,5-Diphenyladipic acid and related compounds
-
Frank, C. E.; Leebrick, J. R.; Moormeier, L. F.; Scheben, J. A., Homberg, O A new synthesis of dibasic acids. II. 2,5-Diphenyladipic acid and related compounds. J. Org. Chem., 1961, 26, 307-309.
-
(1961)
J. Org. Chem
, vol.26
, pp. 307-309
-
-
Frank, C.E.1
Leebrick, J.R.2
Moormeier, L.F.3
Scheben, J.A.4
Homberg, O.5
-
149
-
-
0000429109
-
The disilylation of styrene and α-methylstyrene. The trapping of short-lived intermediates from alkali metals and aryl olefins
-
Weyenberg, D. R.; Toporcer, L. H.; Bey, A. E. The disilylation of styrene and α-methylstyrene. The trapping of short-lived intermediates from alkali metals and aryl olefins. J. Org. Chem., 1965, 30, 4096-4101.
-
(1965)
J. Org. Chem
, vol.30
, pp. 4096-4101
-
-
Weyenberg, D.R.1
Toporcer, L.H.2
Bey, A.E.3
-
150
-
-
0000121574
-
Reductive transformations, 19. Electron-transfer-induced dimerization of β- alkylstyrenes and the structures of the resulting 1,4-dilithiobutanes
-
Schade, P.; Schäfer, T.; Müllen, K.; Bender, D.; Knoll, K.; Bronstert, K. Reductive transformations, 19. Electron-transfer-induced dimerization of β- alkylstyrenes and the structures of the resulting 1,4-dilithiobutanes. Chem. Ber., 1991, 124, 2833-2841.
-
(1991)
Chem. Ber
, vol.124
, pp. 2833-2841
-
-
Schade, P.1
Schäfer, T.2
Müllen, K.3
Bender, D.4
Knoll, K.5
Bronstert, K.6
-
151
-
-
0001731776
-
Unusual electron transfer to styrene and α-methylstyrene mediated by potassium supramolecular complex with 18-crown-6
-
Jedliński, Z.; Czech, A.; Janeczech, H.; Kowalczuk, M. Unusual electron transfer to styrene and α-methylstyrene mediated by potassium supramolecular complex with 18-crown-6. J. Am. Chem. Soc., 1995, 117, 8678-8679.
-
(1995)
J. Am. Chem. Soc
, vol.117
, pp. 8678-8679
-
-
Jedliński, Z.1
Czech, A.2
Janeczech, H.3
Kowalczuk, M.4
-
152
-
-
0001360934
-
Styrene dianions: Two-electron transfer
-
Szwarc, M.; Jedliński, Z.; Janeczech, H. Styrene dianions: two-electron transfer. Macromolecules, 1997, 30, 4498.
-
(1997)
Macromolecules
, vol.30
, pp. 4498
-
-
Szwarc, M.1
Jedliński, Z.2
Janeczech, H.3
-
153
-
-
85196228856
-
-
1H NMR analysis of styrene oligomers evidenced the presence of a methyl group, which can be formed as the end group only by two-electron transfer to styrene
-
1H NMR analysis of styrene oligomers evidenced the presence of a methyl group, which can be formed as the end group only by two-electron transfer to styrene.
-
-
-
-
154
-
-
84981372046
-
Einfache Darstellung von Lithiumdiisopropylamid in molarem Maßstab
-
Reetz, M. T.; Maier, W. F. Einfache Darstellung von Lithiumdiisopropylamid in molarem Maßstab. Liebigs Ann. Chem., 1980, 1471-1473.
-
(1980)
Liebigs Ann. Chem
, pp. 1471-1473
-
-
Reetz, M.T.1
Maier, W.F.2
-
155
-
-
37049108097
-
Protonation kinetics of anionic intermediates in the electrochemical reduction of triphenylethylene: A disproportionation mechanism
-
Farnia, G.; Maran, F.; Sandonà, G.; Severin, M. G. Protonation kinetics of anionic intermediates in the electrochemical reduction of triphenylethylene: a disproportionation mechanism. J. Chem. Soc., Perkin Trans. II, 1982, 1153-1158.
-
(1982)
J. Chem. Soc., Perkin Trans
, vol.2
, pp. 1153-1158
-
-
Farnia, G.1
Maran, F.2
Sandonà, G.3
Severin, M.G.4
-
156
-
-
33847802783
-
Reactions of aromatic anion radicals and dianions. II. Reversible reduction of anion radicals to dianion
-
Jensen, B. S.; Parker, V. D. Reactions of aromatic anion radicals and dianions. II. Reversible reduction of anion radicals to dianions. J. Am. Chem. Soc., 1975, 97, 5211-5217.
-
(1975)
J. Am. Chem. Soc
, vol.97
, pp. 5211-5217
-
-
Jensen, B.S.1
Parker, V.D.2
-
157
-
-
0011618447
-
Protonation of the dianion of tetraphenylethylene by alcohols and water in acetonitrile. Case of mixed first-order and second-order kinetics in the proton donor
-
Farnia, G.; Maran, F.; Sandonà, G. Protonation of the dianion of tetraphenylethylene by alcohols and water in acetonitrile. Case of mixed first-order and second-order kinetics in the proton donor. J. Chem. Soc., Faraday Trans. I, 1986, 82, 1885-1892.
-
(1986)
J. Chem. Soc., Faraday Trans
, vol.1
, Issue.82
, pp. 1885-1892
-
-
Farnia, G.1
Maran, F.2
Sandonà, G.3
-
158
-
-
0035905147
-
DTBB-Catalysed dilithiation of styrene and its methyl-derivatives: Introduction of two electrophilic reagents
-
It is worth noting that this reaction could not be applied to (E)-stilbene or 1,1-diphenylethylene. In these cases either 1,2-diphenylethane or an intractable reaction mixture of products were obtained
-
Yus, M., Martínez, P., Guijarro, D. DTBB-Catalysed dilithiation of styrene and its methyl-derivatives: introduction of two electrophilic reagents. Tetrahedron, 2001, 57, 10119-10124. It is worth noting that this reaction could not be applied to (E)-stilbene or 1,1-diphenylethylene. In these cases either 1,2-diphenylethane or an intractable reaction mixture of products were obtained.
-
(2001)
Tetrahedron
, vol.57
, pp. 10119-10124
-
-
Yus, M.1
Martínez, P.2
Guijarro, D.3
-
159
-
-
37049120837
-
Chemical transformation of the dimeric dianion of 1,1-diphenylethylene
-
Smith, J. G.; Talvitie, J. R.; Eix, A. R. E. Chemical transformation of the dimeric dianion of 1,1-diphenylethylene. J. Chem. Soc., Perkin 1, 1975, 1474-1479.
-
(1975)
J. Chem. Soc., Perkin
, vol.1
, pp. 1474-1479
-
-
Smith, J.G.1
Talvitie, J.R.2
Eix, A.R.E.3
-
160
-
-
7044252549
-
Über Ringspannung und Radikalbildung
-
Wittig, G.; von Lupin, F. Über Ringspannung und Radikalbildung. Chem Ber. 1928, 61, 1627-1634.
-
(1928)
Chem Ber
, vol.61
, pp. 1627-1634
-
-
Wittig, G.1
von Lupin, F.2
-
161
-
-
65949099553
-
1,4-Dilithio- 1,1,4,4-tetraphenylbutane in diethyl ether: An effective initiator for the living anionic polymerization of dienes
-
Dimitrov, P.; Pradeep, I.; Van Beylen, M.; Hogen-Esch, T. E. 1,4-Dilithio- 1,1,4,4-tetraphenylbutane in diethyl ether: an effective initiator for the living anionic polymerization of dienes. J. Polym. Sci. Part A: Polym. Chem., 2009, 47, 2198-2206.
-
(2009)
J. Polym. Sci. Part A: Polym. Chem
, vol.47
, pp. 2198-2206
-
-
Dimitrov, P.1
Pradeep, I.2
van Beylen, M.3
Hogen-Esch, T.E.4
-
162
-
-
0041098023
-
Alkylation of the mono- and disodium adducts of stilbene
-
Reesor, J. W. B.; Smith, J. G.; Wright, G. F. Alkylation of the mono- and disodium adducts of stilbene. J. Org. Chem., 1954, 19, 940-956.
-
(1954)
J. Org. Chem
, vol.19
, pp. 940-956
-
-
Reesor, J.W.B.1
Smith, J.G.2
Wright, G.F.3
-
163
-
-
33644562778
-
Reductive metalation of unsaturated compounds: The effect of allylic protons
-
Smith, J. G.; Wikman, R. T. Reductive metalation of unsaturated compounds: the effect of allylic protons. J. Organomet. Chem., 1973, 49, 91-101.
-
(1973)
J. Organomet. Chem
, vol.49
, pp. 91-101
-
-
Smith, J.G.1
Wikman, R.T.2
-
164
-
-
0007049174
-
Alkylation of the stilbene dianion
-
Smith, J. G.; Oliver, E.; Boettger, T. J. Alkylation of the stilbene dianion. Organometallics, 1983, 2, 1577-1582.
-
(1983)
Organometallics
, vol.2
, pp. 1577-1582
-
-
Smith, J.G.1
Oliver, E.2
Boettger, T.J.3
-
165
-
-
0000451216
-
The addition of alkali metals to phenanthrene
-
Jeanes, A.; Adams, R. The addition of alkali metals to phenanthrene. J. Am. Chem. Soc., 1937, 59, 2608-2622.
-
(1937)
J. Am. Chem. Soc
, vol.59
, pp. 2608-2622
-
-
Jeanes, A.1
Adams, R.2
-
166
-
-
0000848347
-
Synthesis of optically active 10,11-dihydro-5hdibenzo[a,d]cycloheptenes
-
Platzek, J.; Snatzke, G. Synthesis of optically active 10,11-dihydro-5hdibenzo[a,d]cycloheptenes. Tetrahedron, 1987, 43, 4947-4968.
-
(1987)
Tetrahedron
, vol.43
, pp. 4947-4968
-
-
Platzek, J.1
Snatzke, G.2
-
167
-
-
0037415432
-
Primary alkyl fluorides as regioselective alkylating reagents of lithium arene dianions. Easy prediction of regioselectivity by MO calculations on the dianion
-
Herrera, R. P.; Guijarro, A.; Yus, M. Primary alkyl fluorides as regioselective alkylating reagents of lithium arene dianions. Easy prediction of regioselectivity by MO calculations on the dianion. Tetrahedron Lett., 2003, 44, 1313-1316.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 1313-1316
-
-
Herrera, R.P.1
Guijarro, A.2
Yus, M.3
-
168
-
-
36349021382
-
Carbolithiation of simple terminal and strained internal alkenes by the naphthalene and the biphenyl dianion: New modes of reactivity of highly reduced organic species in solution
-
Melero, C.; Guijarro, A.; Baumann, V.; Pérez-Jiménez, Á. J.; Yus, M. Carbolithiation of simple terminal and strained internal alkenes by the naphthalene and the biphenyl dianion: new modes of reactivity of highly reduced organic species in solution. Eur. J. Org. Chem., 2007, 5514-5526.
-
(2007)
Eur. J. Org. Chem
, pp. 5514-5526
-
-
Melero, C.1
Guijarro, A.2
Baumann, V.3
Pérez-Jiménez, A.J.4
Yus, M.5
-
169
-
-
23444442228
-
Reductive metalation of 1,2-diaryl-substituted ethenes: Synthetic applications
-
Azzena, U.; Dettori, G.; Lubinu, C.; Mannu, A.; Pisano, L. Reductive metalation of 1,2-diaryl-substituted ethenes: synthetic applications. Tetrahedron, 2005, 61, 8663-8668.
-
(2005)
Tetrahedron
, vol.61
, pp. 8663-8668
-
-
Azzena, U.1
Dettori, G.2
Lubinu, C.3
Mannu, A.4
Pisano, L.5
-
170
-
-
0141517581
-
Regioselective reductive demethoxylation of 3,4,5-trimethoxystilbenes
-
Azzena, U.; Dettori, G.; Idini, M. V.; Pisano, L.; Sechi, G. Regioselective reductive demethoxylation of 3,4,5-trimethoxystilbenes. Tetrahedron, 2003, 59, 7961-7966.
-
(2003)
Tetrahedron
, vol.59
, pp. 7961-7966
-
-
Azzena, U.1
Dettori, G.2
Idini, M.V.3
Pisano, L.4
Sechi, G.5
-
171
-
-
0009476647
-
Regioselective reductive electrophilic substitution of derivatives of 3,4,5-trimethoxybenzaldehyde
-
Azzena, U., Melloni, G., Piroddi, A. M.; Azara, E.; Contini, S. Regioselective reductive electrophilic substitution of derivatives of 3,4,5-trimethoxybenzaldehyde. J. Org. Chem., 1992, 57, 3101-3106.
-
(1992)
J. Org. Chem
, vol.57
, pp. 3101-3106
-
-
Azzena, U.1
Melloni, G.2
Piroddi, A.M.3
Azara, E.4
Contini, S.5
-
172
-
-
84989479329
-
Delocalized carbanions in synthesis
-
Although the ability of delocalized polycarbanions to act either as nucleophiles or reducing agents towards alkyl halides was already known, reductive elimination of 1,2-dihalides was previously synthetically unexploited; see, for example:, and references therein; see also ref's 107 and 117
-
Although the ability of delocalized polycarbanions to act either as nucleophiles or reducing agents towards alkyl halides was already known, reductive elimination of 1,2-dihalides was previously synthetically unexploited; see, for example: Barry III C. E.; Bates, R. B.; Beavers, W. A.; Camou, F. A.; Gordon III B.; Hsu, H. F.-J.; Mills, S. N.; Ogle, C. A.; Siahaan, T. J.; Suvannachut, K.; Taylor, S. R.; White, J. J.; Yager, K. M. Delocalized carbanions in synthesis. Synlett, 1991, 207-212, and references therein; see also ref's 107 and 117.
-
(1991)
Synlett
, pp. 207-212
-
-
Barry III, C.E.1
Bates, R.B.2
Beavers, W.A.3
Camou, F.A.4
Gordon III, B.5
Hsu, H.F.-J.6
Mills, S.N.7
Ogle, C.A.8
Siahaan, T.J.9
Suvannachut, K.10
Taylor, S.R.11
White, J.J.12
Yager, K.M.13
-
173
-
-
30544447839
-
Reducing Properties of 1,2-diaryl-1,2-disodiumethanes
-
Azzena, U.; Pittalis, M.; Dettori, G.; Madeddu. S.; Azara, E. Reducing properties of 1,2-diaryl-1,2-disodiumethanes. Tetrahedron Lett., 2006, 47, 1055-1058.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 1055-1058
-
-
Azzena, U.1
Pittalis, M.2
Dettori, G.3
Madeddu, S.4
Azara, E.5
-
174
-
-
34548668242
-
A new and highly effective organometallic approach to 1,2-dehalogenations and related reactions
-
Azzena, U.; Pittalis, M.; Dettori, G.; Pisano, L.; Azara, E. A new and highly effective organometallic approach to 1,2-dehalogenations and related reactions. J. Organomet. Chem., 2007, 692, 3892-3900.
-
(2007)
J. Organomet. Chem
, vol.692
, pp. 3892-3900
-
-
Azzena, U.1
Pittalis, M.2
Dettori, G.3
Pisano, L.4
Azara, E.5
-
175
-
-
0000298547
-
1,2-Dehalogenations and Related Reactions
-
Alternative reductive dehalogenation mechanisms are usually described as "single electron" and "concerted two-electrons" reaction pathways. For a comparison between these mechanisms see, Patai, S.; Rappoport, Z. (Eds.), Supplement D, Part I, Wiley: New York
-
Alternative reductive dehalogenation mechanisms are usually described as "single electron" and "concerted two-electrons" reaction pathways. For a comparison between these mechanisms see: Baciocchi, E. 1,2-Dehalogenations and Related Reactions; Patai, S.; Rappoport, Z. (Eds.); in The Chemistry of Functional Groups, Supplement D, Part I, Wiley: New York, 1983, pp. 161-201
-
(1983)
The Chemistry of Functional Groups
, pp. 161-201
-
-
Baciocchi, E.1
-
176
-
-
0003642345
-
Debromination of meso- and (±)-1,2-dibromo-1,2-diphenylethane by 9-substituted fluorenide ions. Correlation between stereochemical results and redox potentials
-
see also
-
see also Lund, T.; Bjørn, C.; Hansen, H. S.; Jensen, A. K.; Thorsen, T. K. Debromination of meso- and (±)-1,2-dibromo-1,2-diphenylethane by 9-substituted fluorenide ions. Correlation between stereochemical results and redox potentials. Acta Chem. Scand., 1993, 47, 877-884.
-
(1993)
Acta Chem. Scand
, vol.47
, pp. 877-884
-
-
Lund, T.1
Bjørn, C.2
Hansen, H.S.3
Jensen, A.K.4
Thorsen, T.K.5
-
177
-
-
70350738417
-
Tuning the reducing properties of 1,2-diaryl-1,2-disodiumethanes
-
Azzena, U., Pisano, L.; Antonello, S.; Maran, F. Tuning the reducing properties of 1,2-diaryl-1,2-disodiumethanes. J. Org. Chem., 2009, 74, 8064-8070.
-
(2009)
J. Org. Chem
, vol.74
, pp. 8064-8070
-
-
Azzena, U.1
Pisano, L.2
Antonello, S.3
Maran, F.4
-
178
-
-
1842317702
-
Lithium-ammonia reduction of aromatic ketones to aromatic hydrocarbons
-
Hall, S. S.; Lipsky, S. D.; McEnroe, F. J.; Bartels, A. P. Lithium-ammonia reduction of aromatic ketones to aromatic hydrocarbons. J. Org. Chem., 1971, 36, 2588-2591.
-
(1971)
J. Org. Chem
, vol.36
, pp. 2588-2591
-
-
Hall, S.S.1
Lipsky, S.D.2
McEnroe, F.J.3
Bartels, A.P.4
-
179
-
-
33947091423
-
Lithiumammonia reduction of benzaldehydes to toluenes
-
Hall, S. S.; Bartels, A. P.; Engman, A. M. Lithiumammonia reduction of benzaldehydes to toluenes. J. Org. Chem., 1972, 37, 760-762.
-
(1972)
J. Org. Chem
, vol.37
, pp. 760-762
-
-
Hall, S.S.1
Bartels, A.P.2
Engman, A.M.3
-
180
-
-
0037458835
-
A novel, solventless reductive coupling of carbonyl compounds by alkali metals, catalysed by bromobenzene
-
Zhao, H.; Li, D.-J.; Deng, L.; Liu, L.; Guo, Q.-X. A novel, solventless reductive coupling of carbonyl compounds by alkali metals, catalysed by bromobenzene. Chem. Commun., 2003, 506-507.
-
(2003)
Chem. Commun
, pp. 506-507
-
-
Zhao, H.1
Li, D.-J.2
Deng, L.3
Liu, L.4
Guo, Q.-X.5
-
181
-
-
1442318931
-
Reductive metalation of benzophenone and benzalacetophenone by alkali metals in liquid ammonia and some condensations of the resulting dialkali salts
-
Hamrick, Jr. P. J.; Hauser, C. R. Reductive metalation of benzophenone and benzalacetophenone by alkali metals in liquid ammonia and some condensations of the resulting dialkali salts. J. Am. Chem. Soc., 1959, 81, 493-496.
-
(1959)
J. Am. Chem. Soc
, vol.81
, pp. 493-496
-
-
Hamrick, P.J.1
Hauser, C.R.2
-
182
-
-
0007599651
-
Synthetic utility of alkali metal adducts of diaryl ketones
-
Selman, S.; Eastham, J. F. Synthetic utility of alkali metal adducts of diaryl ketones. J. Org. Chem., 1965, 30, 3804-3809.
-
(1965)
J. Org. Chem
, vol.30
, pp. 3804-3809
-
-
Selman, S.1
Eastham, J.F.2
-
183
-
-
21844447037
-
Alkylation of benzophenone with aminoalkyl halides in liquid ammonia
-
Anderson, E. L.; Casey, Jr. J. C. Alkylation of benzophenone with aminoalkyl halides in liquid ammonia. J. Org. Chem., 1965, 30, 3959-3960.
-
(1965)
J. Org. Chem
, vol.30
, pp. 3959-3960
-
-
Anderson, E.L.1
Casey, J.C.2
-
184
-
-
15744405980
-
Nucleophilic displacement of one dianion by another
-
Zaugg, H. E.; Michaels, R. J. Nucleophilic displacement of one dianion by another. J. Org. Chem., 1968, 33, 2167-2169.
-
(1968)
J. Org. Chem
, vol.33
, pp. 2167-2169
-
-
Zaugg, H.E.1
Michaels, R.J.2
-
185
-
-
0026081472
-
Synthesis and antiarrhythmic activity oof cis-2,6-dimethyl-α.α-diaryl-1-piperidinebutanols
-
Hoefle, M. L.; Blouin, L. T.; Fleming, R. W.; Hastings, S.; Hinkley, J. M.; Mertz, T. E.; Steffe, T. J.; Stratton, C. S. Synthesis and antiarrhythmic activity oof cis-2,6-dimethyl-α.α-diaryl-1-piperidinebutanols. J. Med. Chem., 1991, 34, 12-19.
-
(1991)
J. Med. Chem
, vol.34
, pp. 12-19
-
-
Hoefle, M.L.1
Blouin, L.T.2
Fleming, R.W.3
Hastings, S.4
Hinkley, J.M.5
Mertz, T.E.6
Steffe, T.J.7
Stratton, C.S.8
-
186
-
-
0001657729
-
Interaction between alkali metal aromatic ketone radical anions and the chlorides of lithium and magnesium in solution. A case of a carbon-carbon bond strengthening through complex formation
-
It is however interesting to observe that, under appropriate quenching conditions, reactions run in liquid NH3 could lead to the formation of the corresponding hydrocarbons (250); see ref. 137a. Furthermore, treatment of a THF solution of lithium benzophenone radical anion with MgCl2, followed by acidic quenching, led to the quantitative recovery of the corresponding pinacols
-
It is however interesting to observe that, under appropriate quenching conditions, reactions run in liquid NH3 could lead to the formation of the corresponding hydrocarbons (250); see ref. 137a. Furthermore, treatment of a THF solution of lithium benzophenone radical anion with MgCl2, followed by acidic quenching, led to the quantitative recovery of the corresponding pinacols: Micha-Screttas, M.; Heropoulos, G. A.; Steele, B. R. Interaction between alkali metal aromatic ketone radical anions and the chlorides of lithium and magnesium in solution. A case of a carbon-carbon bond strengthening through complex formation. J. Chem. Soc., Perkin Trans. 2, 1999, 2685-2690.
-
(1999)
J. Chem. Soc., Perkin Trans
, vol.2
, pp. 2685-2690
-
-
Micha-Screttas, M.1
Heropoulos, G.A.2
Steele, B.R.3
-
187
-
-
8344277203
-
The reaction of aromatic ketones with sodium. i. The structure of the so-called metal ketyls
-
see also
-
see also: Bachmann, W. E. The reaction of aromatic ketones with sodium. i. The structure of the so-called metal ketyls. J. Am. Chem. Soc., 1933, 55, 1179-1188.
-
(1933)
J. Am. Chem. Soc
, vol.55
, pp. 1179-1188
-
-
Bachmann, W.E.1
-
188
-
-
0041609163
-
Reactions of the stilbene-disodium and -dilithium adducts
-
Brook, A. G.; Cohen, H. L.; Wright, G. F. Reactions of the stilbene-disodium and -dilithium adducts. J. Org. Chem., 1953, 18, 447-463.
-
(1953)
J. Org. Chem
, vol.18
, pp. 447-463
-
-
Brook, A.G.1
Cohen, H.L.2
Wright, G.F.3
-
189
-
-
0027416797
-
O-Dilithiated diarylmethanols: Easy and improved preparation by naphthalene-catalysed lithiation of diaryl ketones and reactivity toward electrophiles
-
Guijarro, D.; Mancheño, B.; Yus, M. C,O-Dilithiated diarylmethanols: easy and improved preparation by naphthalene-catalysed lithiation of diaryl ketones and reactivity toward electrophiles. Tetrahedron 1993, 49, 1327-1334.
-
(1993)
Tetrahedron
, vol.49
, pp. 1327-1334
-
-
Guijarro, D.1
Mancheño, B.2
Yus, M.C.3
-
190
-
-
0025048422
-
Conversion of aromatic ketones, benzyl alcohols, and alkyl aryl ethers to aromatic hydrocarbons with lithium 4,4'-di-t-butylbiphenyl radical anion
-
Karaman, R.; Kohlman, D. T.; Fry, J. L. Conversion of aromatic ketones, benzyl alcohols, and alkyl aryl ethers to aromatic hydrocarbons with lithium 4,4'-di-t-butylbiphenyl radical anion. Tetrahedron Lett., 1990, 31, 6155-6158.
-
(1990)
Tetrahedron Lett
, vol.31
, pp. 6155-6158
-
-
Karaman, R.1
Kohlman, D.T.2
Fry, J.L.3
-
191
-
-
0001308623
-
Stereochemistry of the bimolecular metal reduction of benzalaniline
-
and references therein
-
Eisch, J. J.; Kaska, D. D.; Peterson, C. J. Stereochemistry of the bimolecular metal reduction of benzalaniline. J. Org. Chem., 1966, 31, 453-456, and references therein.
-
(1966)
J. Org. Chem
, vol.31
, pp. 453-456
-
-
Eisch, J.J.1
Kaska, D.D.2
Peterson, C.J.3
-
192
-
-
0000060229
-
Reductive dimerization of Schiff bases by alkali metals. Isomerization of the dimeric dianions
-
Smith, J. G.; Ho, I. Reductive dimerization of Schiff bases by alkali metals. Isomerization of the dimeric dianions. J. Org. Chem., 1972, 37, 653-656.
-
(1972)
J. Org. Chem
, vol.37
, pp. 653-656
-
-
Smith, J.G.1
Ho, I.2
-
193
-
-
0343990268
-
The reactions of the disodium adduct of benzophenone anil
-
Smith, J. G.; Veach, C. D. The reactions of the disodium adduct of benzophenone anil. Can. J. Chem., 1966, 44, 2245-2257.
-
(1966)
Can. J. Chem
, vol.44
, pp. 2245-2257
-
-
Smith, J.G.1
Veach, C.D.2
-
194
-
-
0027304142
-
Naphthalene-catalysed lithiation of phenone imines in the presence of carbonyl compounds: Preparation of 1,2-aminoalcohols
-
Guijarro, D.; Yus, M. Naphthalene-catalysed lithiation of phenone imines in the presence of carbonyl compounds: preparation of 1,2-aminoalcohols. Tetrahedron, 1993, 49, 7761-7768.
-
(1993)
Tetrahedron
, vol.49
, pp. 7761-7768
-
-
Guijarro, D.1
Yus, M.2
|