Diastereoselective Synthesis of Pentasubstituted γ??Butyrolactones from Silyl Glyoxylates and Ketones through a Double Reformatsky Reaction
SN Greszler, JS Johnson
Index: Greszler, Stephen N.; Johnson, Jeffrey S. Angewandte Chemie, International Edition, 2009 , vol. 48, # 20 p. 3689 - 3691
Full Text: HTML
Citation Number: 46
Abstract
Abstract Three contiguous stereocenters can be established with remarkable diastereoselectivity in a double Reformatsky sequence. Densely functionalized γ- butyrolactones were assembled rapidly by this approach, in which a ketone is used as the terminal electrophile (see scheme). Secondary transformations of the lactone products enhance their synthetic utility. R 1= Me, H; R 2= alkyl, aryl, CF 3; Bn= benzyl, TBS= tert- ...
Related Articles:
[Lee, Seung Hwan; Cho, Min Young; Nam, Mi Hye; Park, Young Sang; Yoo, Byung Woo; Lee, Chi-Woo; Yoon, Cheol Min Synthetic Communications, 2005 , vol. 35, # 10 p. 1335 - 1341]
[Qian, Wangke; Zhang, Lei; Sun, Haifeng; Jiang, Hualiang; Liu, Hong Advanced Synthesis and Catalysis, 2012 , vol. 354, # 17 p. 3231 - 3236]
[Koos, Peter; Gross, Ulrike; Polyzos, Anastasios; O'Brien, Matthew; Baxendale, Ian; Ley, Steven V. Organic and Biomolecular Chemistry, 2011 , vol. 9, # 20 p. 6903 - 6908]
[Renga, James M.; Wang, Pen-Chung Synthetic Communications, 1984 , vol. 14, # 1 p. 77 - 82]
[Barcia, Jose C; Cruces, Jacobo; Estevez, Juan C; Estevez, Ramon J; Castedo, Luis Tetrahedron Letters, 2002 , vol. 43, # 29 p. 5141 - 5144]