By Edwin Vedejs

This quantity displays the in depth task in numerous parts of artificial natural chemistry, equivalent to enol/carbonyl condensations; alkynes, alkenes and fragrant carbocycles; heteroelement chemistry (with recognize to organosilicon reagents, transition aspect chemistry, and within the instruction of-lactams and indoles); and chiral auxiliaries.

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Am. Chem. , 135, 19016–19024. , and 27 28 1 Lewis Acid–Brønsted Base Catalysis 37. 38. 39. 40. 41. 42. 43. 44. 45. 46. J. (2013) Organometallics, 32, 7431–7439. , and Shibasaki, M. (1996) Angew. , Int. Ed. , 35, 104–106. For the previously known asymmetric monometallic Al-1,1′ -binaphthoxide reagents and related compounds, see: Noyori, R. (1994) Tetrahedron, 50, 4259–4292. , and Shibasaki, M. (1998) J. Am. Chem. , 120, 441–442. , and Shibasaki, M. , and Shibasaki, M. (2002) J. Am. Chem. , 124, 14546–14547.

2013) Angew. Chem. Int. , 52, 223–234. , and Shibasaki, M. (2007) J. Am. Chem. , and Shibasaki, M. References 111. 112. 113. 114. 115. 116. 117. 118. (2008) Org. , and Shibasaki, M. (2008) J. Am. Chem. , and Mashiko, T. (2009) Org. , and Shibasaki, M. (2009) J. Am. Chem. , and Shibasaki, M. (2009) J. Am. Chem. , and Shibasaki, M. (2010) Org. , and Shibasaki, M. (2010) Chem. Eur. , and Shibasaki, M. , and Shibasaki, M. (2012) Angew. Chem. Int. , and Shibasaki, M. (2013) Chem. , 49, 4628–4630. , and Shibasaki, M.

2005) Org. , and Zhu, C. , 50, 548–551. For reviews, see: (a) Shibasaki, M. and Matsunaga, S. (2010) J. Synth. Org. Chem. , 68, 1142–1149; (b) Matsunaga, S. and Shibasaki, M. (2014) Chem. , 50, 1044–1057. , and Okawa, H. (2001) Coord. Chem. A. (1994) Inorg. Chim. -P. (1998) Chem. Eur. , and Dupuis, A. (2000) Inorg. , and Sudoh, S. , and Stanica, N. , and Mohanta, S. (2005) Eur. J. Inorg. , and Mohanta, S. (2005) Inorg. , and Ephritikhine, M. (2006) Inorg. , 45, 83–93. , and Shibasaki, M. (2007) 84.

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