阿赫馬托維奇反應是呋喃轉變為二氫吡喃環的過程,1971年由小奧斯曼·阿赫馬托維奇發現。[1] 最初方法是用糠醇與溴在甲醇中反應,先得到2,5-二甲氧基-二氫糠醇,它用稀硫酸發生重排便得到一個二氫吡喃衍生物。該衍生物與原甲酸甲酯和三氟化硼反應上甲基保護基,接着用硼氫化鈉還原酮基,可得另一二氫吡喃衍生物,這個產物可用作許多單糖的合成中間體。
這個反應用於天然產物desoxoprosophylline[2]、核球殼菌素(Pyrenophorin)[3]和包公藤甲素(Bao Gong Teng A)[4] 和全合成中。
最近也用於定向多樣性合成 [5] [6]
以及 enantiomeric scaffolding 中。[7][8]
Synthesis of methyl 2,3-dideoxy--alk-2-enopyranosides from furan compounds : A general approach to the total synthesis of monosaccharides Tetrahedron, Volume 27, Issue 10, 1971, Pages 1973-1996 O. Achmatowicz, P. Bukowski, B. Szechner, Z. Zwierzchowska and A. Zamojski doi:10.1016/S0040-4020(01)98229-8
Efficient Conditions for Conversion of 2-Substituted Furans into 4-Oxygenated 2-Enoic Acids and Its Application to Synthesis of (+)-Aspicilin, (+)-Patulolide A, and (-)-Pyrenophorin Kobayashi, Y.; Nakano, M.; Kumar, G. B.; Kishihara, K. J. Org. Chem.; (Article); 1998; 63(21); 7505-7515. doi:10.1021/jo980942a
Organometallic Enantiomeric Scaffolding: Organometallic Chirons. Total Synthesis of (-)-Bao Gong Teng A by a Molybdenum-Mediated [5+2] Cycloaddition
Yongqiang Zhang and Lanny S. Liebeskind J. Am. Chem. Soc. 2006; 128(2) pp 465 - 472; (Article) doi:10.1021/ja055623x
A Synthesis Strategy Yielding Skeletally Diverse Small Molecules Combinatorially
Martin D. Burke, Eric M. Berger, and Stuart L. Schreiber J. Am. Chem. Soc. 126 (43), 14095 -14104, 2004. doi:10.1021/ja0457415
Practical, Scalable, High-Throughput Approaches to 3-Pyranyl and 3-Pyridinyl Organometallic Enantiomeric Scaffolds Using the Achmatowicz Reaction Thomas C. Coombs, Maurice D. Lee, IV, Heilam Wong, Matthew Armstrong, Bo Cheng, Wenyong Chen, Alessandro F. Moretto, and Lanny S. Liebeskind J. Org. Chem. 73 (3), 882 -888, 2008. doi:10.1021/jo702006z