An Alternative Method for the Highly Selective Iodination of Alcohols Using a CsI/BF3·Et2O System
摘要:
A variety of allylic and benzylic alcohols have been converted into the corresponding iodides using cesium iodide (CsI) in the presence of boron trifluoride etherate (BF3.Et2O) in acetonitrile under mild conditions.
General method for the synthesis of cyclic peptidomimetic compounds
作者:Michael A Walker、Timothy Johnson
DOI:10.1016/s0040-4039(01)01134-0
日期:2001.8
A number of cyclic peptides, wherein the i and i+1 residue side chains are joined by an alkyl linker and a Weinreb amide is present at the C-terminus, were synthesized. Using LiCl to solubilize these peptides in THF the C-terminus can be readily converted to an activated carbonyl such as an aldehyde or ketone. (C) 2001 Elsevier Science Ltd. All rights reserved.
Hudson et al., Journal of the Chemical Society B: Physical Organic, 1967, p. 1069,1070
作者:Hudson et al.
DOI:——
日期:——
An Alternative Method for the Highly Selective Iodination of Alcohols Using a CsI/BF<sub>3</sub>·Et<sub>2</sub>O System
作者:Safdar Hayat、Atta-ur-Rahman、Khalid Mohammed Khan、M. Iqbal Choudhary、Ghulam Murtaza Maharvi、Zia-Ullah、Ernst Bayer
DOI:10.1081/scc-120021844
日期:2003.1.8
A variety of allylic and benzylic alcohols have been converted into the corresponding iodides using cesium iodide (CsI) in the presence of boron trifluoride etherate (BF3.Et2O) in acetonitrile under mild conditions.
Petrow, Doklady Akademii Nauk SSSR, 1950, vol. 72, p. 515