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Takacs, J. M.; Vayalakkada, S., Science of Synthesis, (2001) 1, 374..
Enolate Claisen Rearrangements
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Science of Synthesis
Green, J. R., Science of Synthesis, (2006) 8, 463..
Electrophile Incorporation: Reaction with Carboxy Compounds (C—Li → C—C=X)
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Science of Synthesis
Chataigner, I.; Harrison-Marchand, A.; Maddaluno, J., Science of Synthesis, (2005) 26, 1149..
With Acyl Halides and Acyl Cyanides
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Science of Synthesis
Green, J. R., Science of Synthesis, (2006) 8, 468..
Electrophile Incorporation: Michael Addition (C—Li → C—C—C—C=X)
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Science of Synthesis
Gennari, C.; Ceccarelli, S.; Piarulli, U., Science of Synthesis, (2005) 6, 367..
From Imide-Derived Vinyloxyboranes
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Science of Synthesis
Kawahara, Shigeru; Gaunt, Matthew J.; Scolaro, Alessandra; Yamanoi, Shigeo; Ley, Steven V., Synlett 2005, 2031-2034.
Synthesis of the EF Fragment of Spongistatin 1
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Synlett
[DOI: 10.1055/s-2005-871960]
Mahrwald, R.; Schetter, B., Science of Synthesis, (2008) 36, 868..
Additions to Titanium Enolates
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Science of Synthesis
Mahrwald, R.; Schetter, B., Science of Synthesis, (2008) 36, 860..
Additions to Boron Enolates
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Science of Synthesis
Masse, C. E., Science of Synthesis, (2007) 20, 1031..
Succinate Esters by Asymmetric Alkylation Using N-Acyloxazolidinones (Evans Asymmetric Alkylation)
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Science of Synthesis
Gleason, J. L.; Tiong, E. A., Science of Synthesis Knowledge Updates, (2010) 4, 289..
Chiral Auxiliaries: Tertiary Stereocenters
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Science of Synthesis
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