A study of the functional group compatibility of sulfoximination methods

被引:25
作者
Cren, S [1 ]
Kinahan, TC [1 ]
Skinner, CL [1 ]
Tye, H [1 ]
机构
[1] Univ Birmingham, Sch Chem Sci, Birmingham B15 2TT, W Midlands, England
关键词
D O I
10.1016/S0040-4039(02)00378-7
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The sulfoximination of a range of sulfoxides possessing functionalised side-chains using mesitylene sulfonyl hydroxyl-amine or iminoiodane reagents is discussed. The use of iminoiodane reagents possessing removable protecting groups (p-nosyl and Ses) is reported along with conditions for the deprotection of the sulfoximine adducts. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2749 / 2751
页数:3
相关论文
共 9 条
[1]  
Bolm C, 2001, CHEM-EUR J, V7, P1118, DOI 10.1002/1521-3765(20010302)7:5<1118::AID-CHEM1118>3.0.CO
[2]  
2-3
[3]  
Bolm C, 1999, SYNTHESIS-STUTTGART, P1251
[4]   PhI=NSes: A new iminoiodinane reagent for the copper-catalyzed aziridination of olefins [J].
Dauban, P ;
Dodd, RH .
JOURNAL OF ORGANIC CHEMISTRY, 1999, 64 (14) :5304-5307
[5]   SYNTHESIS OF OPTICALLY-ACTIVE SULFOXIMINES FROM OPTICALLY-ACTIVE SULFOXIDES [J].
JOHNSON, CR ;
KIRCHHOF.RA ;
CORKINS, HG .
JOURNAL OF ORGANIC CHEMISTRY, 1974, 39 (16) :2458-2459
[6]   DESIGN AND SYNTHESIS OF TETRAHEDRAL INTERMEDIATE ANALOGS AS POTENTIAL DIHYDROOROTASE INHIBITORS [J].
LEVENSON, CH ;
MEYER, RB .
JOURNAL OF MEDICINAL CHEMISTRY, 1984, 27 (02) :228-232
[7]   Cu(I)-catalyzed sulfoximination [J].
Müller, JFK ;
Vogt, P .
TETRAHEDRON LETTERS, 1998, 39 (27) :4805-4806
[8]  
Reggelin M, 2000, SYNTHESIS-STUTTGART, P1
[9]  
TAMURA Y, 1977, SYNTHESIS-STUTTGART, P1