施洛瑟鹼 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "施洛瑟鹼" in Chinese language version.

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3wiley.com

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L. Lochmann, J. Pospíšil, J. Vodňanský, J. Trekoval, D. Lím. Interaction of alkyl lithium compounds with lithium alcoholates. Collect. Czech. Chem. Commun. 1965, 30 (7): 2187-2195 [2015-12-16]. doi:10.1135/cccc19652187. （原始内容存档于2019-06-04）（英语）.
L. Lochmann, R. Lukáš, D. Lím. Effect of lithium alkoxides on the rate of the reaction between butyllithium and 1,1-diphenylethylene. Collect. Czech. Chem. Commun. 1972, 37: 569 [2015-12-17]. doi:10.1135/cccc19720569. （原始内容存档于2019-06-04）（英语）.

doi.org

Manfred Schlosser, Sven Strunk. The “super-basic” butyllithium/potassium tert-butoxide mixture and other lickor-reagent. Tetrahedron Lett. 1984, 25 (7): 741-744. doi:10.1016/S0040-4039(01)80014-9.
Lubomír Lochmann, Miroslav Janata. 50 years of superbases made from organolithium compounds and heavier alkali metal alkoxides. Cent. Eur. J. Chem. 2014, 12 (5): 537-548 [2015-12-16]. doi:10.2478/s11532-014-0528-0. （原始内容存档于2019-06-29）（英语）.
Schlosser, M. Superbases for organic synthesis. Pure and Applied Chemistry. 1988, 60: 1627 [2015-12-13]. doi:10.1351/pac198860111627. （原始内容存档于2016-06-28）（英语）.
L. Lochmann, J. Pospíšil, J. Vodňanský, J. Trekoval, D. Lím. Interaction of alkyl lithium compounds with lithium alcoholates. Collect. Czech. Chem. Commun. 1965, 30 (7): 2187-2195 [2015-12-16]. doi:10.1135/cccc19652187. （原始内容存档于2019-06-04）（英语）.
M. Marsch, K. Harms, L. Lochmann, G. Boche. [nBuLi · LiOtBu]4, Solid-State Structure of ann-Butyllithium–Lithium tert-Butoxide Complex. Angew. Chem. Int. Ed. 1990, 29 (3): 308-309. doi:10.1002/anie.199003081 （英语）.
L. Lochmann, R. Lukáš, D. Lím. Effect of lithium alkoxides on the rate of the reaction between butyllithium and 1,1-diphenylethylene. Collect. Czech. Chem. Commun. 1972, 37: 569 [2015-12-17]. doi:10.1135/cccc19720569. （原始内容存档于2019-06-04）（英语）.
L. Lochmann, J. Pospíšil, D. Lím. On the interaction of organolithium compounds with sodium and potassium alkoxides. A new method for the synthesis of organosodium and organopotassium compounds. Tetrahedron Lett. 1966, 7 (2): 257-262. doi:10.1016/S0040-4039(00)70224-3 （英语）.
M. Schlosser. Zur aktivierung lithiumorganischer reagenzien. J. Oganomet. Chem. 1967, 8 (1): 9. doi:10.1016/S0022-328X(00)84698-7 （德语）.
M. Schlosser, J. Hartmann. Transmetalation and Double Metal Exchange: A Convenient Route to Organolithium Compounds of the Benzyl and Allyl Type. Angew. Chem. Int. Ed. 1973, 12 (6): 508-509. doi:10.1002/anie.197305082 （英语）.
M. Schlosse. Prescriptions and Ingredients for Controlled CC Bond Formation with Organometallic Reagents. New synthetic methods. Angew. Chem. Int. Ed. 1974, 13 (11): 701-706. doi:10.1002/anie.197407011 （英语）.
T. Narita, T. Tsuruta. The ionic character of organolithium compounds in the presence of lithium methoxyethoxide: “Coordination-agent-separated” ion pairs. J. Organomet. Chem. 1971, 30: 289. doi:10.1016/S0022-328X(00)87512-9 （英语）.
N. Nugay, T. Nugay, R. Jerome, P. Teyssie. Lithiation of toluene by organolithium compounds activated by lithium polyether alkoxides. J. Mol. Catal. A-Chem. 2002, 179: 59. doi:10.1016/S1381-1169(01)00385-5 （英语）.

iupac.org

Schlosser, M. Superbases for organic synthesis. Pure and Applied Chemistry. 1988, 60: 1627 [2015-12-13]. doi:10.1351/pac198860111627. （原始内容存档于2016-06-28）（英语）.

sciencedirect.com

Manfred Schlosser, Sven Strunk. The “super-basic” butyllithium/potassium tert-butoxide mixture and other lickor-reagent. Tetrahedron Lett. 1984, 25 (7): 741-744. doi:10.1016/S0040-4039(01)80014-9.
L. Lochmann, J. Pospíšil, D. Lím. On the interaction of organolithium compounds with sodium and potassium alkoxides. A new method for the synthesis of organosodium and organopotassium compounds. Tetrahedron Lett. 1966, 7 (2): 257-262. doi:10.1016/S0040-4039(00)70224-3 （英语）.
M. Schlosser. Zur aktivierung lithiumorganischer reagenzien. J. Oganomet. Chem. 1967, 8 (1): 9. doi:10.1016/S0022-328X(00)84698-7 （德语）.
T. Narita, T. Tsuruta. The ionic character of organolithium compounds in the presence of lithium methoxyethoxide: “Coordination-agent-separated” ion pairs. J. Organomet. Chem. 1971, 30: 289. doi:10.1016/S0022-328X(00)87512-9 （英语）.
N. Nugay, T. Nugay, R. Jerome, P. Teyssie. Lithiation of toluene by organolithium compounds activated by lithium polyether alkoxides. J. Mol. Catal. A-Chem. 2002, 179: 59. doi:10.1016/S1381-1169(01)00385-5 （英语）.

springer.com

link.springer.com

Lubomír Lochmann, Miroslav Janata. 50 years of superbases made from organolithium compounds and heavier alkali metal alkoxides. Cent. Eur. J. Chem. 2014, 12 (5): 537-548 [2015-12-16]. doi:10.2478/s11532-014-0528-0. （原始内容存档于2019-06-29）（英语）.

web.archive.org

Lubomír Lochmann, Miroslav Janata. 50 years of superbases made from organolithium compounds and heavier alkali metal alkoxides. Cent. Eur. J. Chem. 2014, 12 (5): 537-548 [2015-12-16]. doi:10.2478/s11532-014-0528-0. （原始内容存档于2019-06-29）（英语）.
Schlosser, M. Superbases for organic synthesis. Pure and Applied Chemistry. 1988, 60: 1627 [2015-12-13]. doi:10.1351/pac198860111627. （原始内容存档于2016-06-28）（英语）.
L. Lochmann, J. Pospíšil, J. Vodňanský, J. Trekoval, D. Lím. Interaction of alkyl lithium compounds with lithium alcoholates. Collect. Czech. Chem. Commun. 1965, 30 (7): 2187-2195 [2015-12-16]. doi:10.1135/cccc19652187. （原始内容存档于2019-06-04）（英语）.
L. Lochmann, R. Lukáš, D. Lím. Effect of lithium alkoxides on the rate of the reaction between butyllithium and 1,1-diphenylethylene. Collect. Czech. Chem. Commun. 1972, 37: 569 [2015-12-17]. doi:10.1135/cccc19720569. （原始内容存档于2019-06-04）（英语）.

wiley.com

onlinelibrary.wiley.com

M. Marsch, K. Harms, L. Lochmann, G. Boche. [nBuLi · LiOtBu]4, Solid-State Structure of ann-Butyllithium–Lithium tert-Butoxide Complex. Angew. Chem. Int. Ed. 1990, 29 (3): 308-309. doi:10.1002/anie.199003081 （英语）.
M. Schlosser, J. Hartmann. Transmetalation and Double Metal Exchange: A Convenient Route to Organolithium Compounds of the Benzyl and Allyl Type. Angew. Chem. Int. Ed. 1973, 12 (6): 508-509. doi:10.1002/anie.197305082 （英语）.
M. Schlosse. Prescriptions and Ingredients for Controlled CC Bond Formation with Organometallic Reagents. New synthetic methods. Angew. Chem. Int. Ed. 1974, 13 (11): 701-706. doi:10.1002/anie.197407011 （英语）.