Green Approaches To Asymmetric Catalytic Synthesis by Angela Patti

By Angela Patti

Nowadays, chirality is broadly authorized as an incredible think about molecular attractiveness strategies and the organic job of many pharmaceutical medications and agrochemicals; this can be proven via the continual want for artificial equipment which bring about unmarried or enriched enantiomers of such compounds.

By proposing a overview of some of the and extra lately built techniques for either metal-transition and organocatalysis, this quantity describes the advance of “greener” uneven reactions which look after stereoselectivity.

The writer summarizes the extraordinary volume of analysis that has been collected inside this box into 3 chapters concentrating on: i)the seek of other catalysts, ii) substitute solvents, and iii) replacement artificial innovations and procedures. for every subject, the basics and a few beneficial purposes are discussed.

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88. 89. 90. 91. 92. 93. 94. 95. 96. 97. 98. 99. 100. 101. 102. 103. 104. 105. 106. 107. 108. 109. 110. 111. 112. 113. 114. 115. 116. 1 Methods for the Preparation of Optically Active Chiral Compounds Lin GQ, Xu MH, Zhong YW, Sun XW (2008) Acc Chem Res 41:831–840 Harold T, Hoffmann RW (1978) Angew Chem Int Ed 17:768–769 Roush WR, Walts AE, Hoong LK (1985) J Am Chem Soc 107:8186–8190 Jadhav PK, Bhat KS, Perumal T, Brown HC (1986) J Org Chem 51:432–439 Burgos CH, Canales E, Matos K, Soderquist JA (2005) J Am Chem Soc 127:8044–8049 Brown HC, Ramachandran PVI (1991) Pure Appl Chem 63:307–316 Paterson I (1992) Pure Appl Chem 64:1821–1830 Masamune S, Sato T, Kim B, Wollmann TA (1986) J Am Chem Soc 108:8279–8281 Corey EJ, Kim SS (1990) J Am Chem Soc 117:4976–4977 Gonzalez AZ, Román JG, Gonzalez E, Martinez J, Medina JR, Matos K, Soderquist JA (2008) J Am Chem Soc 130:9218–9219 Thomas SP, Aggarwal VK (2009) Angew Chem Int Ed 48:1896–1898 Rasor PJ, Voss E (2001) Appl Catal A Gen 221:45–158 Breuer M, Ditrich K, Habicher T, Hauer B, Keßeler M, Stürmer R, Zelinsky T (2004) Angew Chem Int Ed 43:788–824 Nozaki H, Moriuti S, Takaya H, Noyori R (1966) Tetrahedron Lett 7:5239–5244 Knowles WS, Sabacky MJ, Vineyard BD (1977) US Patent 4005127, 25 January 1977 Knowles WS (2002) Angew Chem Int Ed 41:1998–2007 (Nobel Lecture) Noyori R (2002) Angew Chem Int Ed 41:2008–2022 (Nobel Lecture) Sharpless BK (2002) Angew Chem Int Ed 41:2024–2032 (Nobel Lecture) Knowles WS (1983) Acc Chem Res 16:106–112 Tang W, Zhang X (2003) Chem.

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83. 84. 85. 86. 87. 88. 89. 90. 91. 92. 93. 94. 95. 96. 97. 98. 99. 100. 101. 102. 103. 104. 105. 106. 107. 108. 109. 110. 111. 112. 113. 114. 115. 116. 1 Methods for the Preparation of Optically Active Chiral Compounds Lin GQ, Xu MH, Zhong YW, Sun XW (2008) Acc Chem Res 41:831–840 Harold T, Hoffmann RW (1978) Angew Chem Int Ed 17:768–769 Roush WR, Walts AE, Hoong LK (1985) J Am Chem Soc 107:8186–8190 Jadhav PK, Bhat KS, Perumal T, Brown HC (1986) J Org Chem 51:432–439 Burgos CH, Canales E, Matos K, Soderquist JA (2005) J Am Chem Soc 127:8044–8049 Brown HC, Ramachandran PVI (1991) Pure Appl Chem 63:307–316 Paterson I (1992) Pure Appl Chem 64:1821–1830 Masamune S, Sato T, Kim B, Wollmann TA (1986) J Am Chem Soc 108:8279–8281 Corey EJ, Kim SS (1990) J Am Chem Soc 117:4976–4977 Gonzalez AZ, Román JG, Gonzalez E, Martinez J, Medina JR, Matos K, Soderquist JA (2008) J Am Chem Soc 130:9218–9219 Thomas SP, Aggarwal VK (2009) Angew Chem Int Ed 48:1896–1898 Rasor PJ, Voss E (2001) Appl Catal A Gen 221:45–158 Breuer M, Ditrich K, Habicher T, Hauer B, Keßeler M, Stürmer R, Zelinsky T (2004) Angew Chem Int Ed 43:788–824 Nozaki H, Moriuti S, Takaya H, Noyori R (1966) Tetrahedron Lett 7:5239–5244 Knowles WS, Sabacky MJ, Vineyard BD (1977) US Patent 4005127, 25 January 1977 Knowles WS (2002) Angew Chem Int Ed 41:1998–2007 (Nobel Lecture) Noyori R (2002) Angew Chem Int Ed 41:2008–2022 (Nobel Lecture) Sharpless BK (2002) Angew Chem Int Ed 41:2024–2032 (Nobel Lecture) Knowles WS (1983) Acc Chem Res 16:106–112 Tang W, Zhang X (2003) Chem.

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