Neighboring group participation in Lewis acid-promoted [3 + 4] and [3 + 5] annulations. The synthesis of oxabicyclo[3.n.1]alkan-3-ones
作者:Gary A. Molander、Kimberly O. Cameron
DOI:10.1021/ja00056a002
日期:1993.2
2-(alkoxycarbon)-m-oxabicyclo[3.n.1]alkan-3-ones can be constructed by this process in which two new carbon-carbon bonds are generated. Unusually high regioncontrol is observed, and good to excellent stereochemicalcontrol can be achieved at virtually every position on the new carbocycles. Intramolecular neighboringgroupparticipation is proposed to explain the unusually high selectivities attained in the annulation
Cooperative Catalysis of Samarium Diiodide and Mercaptan in a Stereoselective One-Pot Transformation of 5-Oxopentanals into δ-Lactones
作者:Jue-Liang Hsu、Chao-Tsen Chen、Jim-Min Fang
DOI:10.1021/ol9911526
日期:1999.12.1
[GRAPHICS]We demonstrate a general method for conversion of various 5-oxopentanals to substituted delta-lactones and 1-oxa-2-decalones by the synergistic catalysis of samarium diiodide and 2-propanethiol (or disulfide), The deliberate use of mercaptan is advantageous to facilitate the catalytic cycle, This method shows high stereoselectivities, and an enantioselective procedure is feasible by using the chiral mercaptan (1R,2S)-1 phenyl-2-(N-acetamido)propanethiol as a promoter.
Epsztajn, Jan; Bieniek, Adam; Brzezinski, Jacek Z., Polish Journal of Chemistry, 1980, vol. 54, # 2, p. 341 - 347
作者:Epsztajn, Jan、Bieniek, Adam、Brzezinski, Jacek Z.
DOI:——
日期:——
EPSZTAJN J.; BIENIEK A.; BRZEZINSKI J. Z., POL. J. CHEM., 1980, 54, NO 2, 341-347
作者:EPSZTAJN J.、 BIENIEK A.、 BRZEZINSKI J. Z.
DOI:——
日期:——
Stereoselective Synthesis of δ-Lactones from 5-Oxoalkanals via One-Pot Sequential Acetalization, Tishchenko Reaction, and Lactonization by Cooperative Catalysis of Samarium Ion and Mercaptan
作者:Jue-Liang Hsu、Jim-Min Fang
DOI:10.1021/jo016058t
日期:2001.12.1
sequence of acetalization, Tishchenko reaction and lactonization. The deliberative use of mercaptan, by comparison with alcohol, is advantageous to facilitate the catalytic cycle. The reaction mechanism and stereochemistry are proposed and supported by some experimental evidence. Such samarium ion/mercaptan cocatalyzed reactions show the feature of remote control, which is applicable to the asymmetric synthesis