Second generation fluorous DEAD reagents have expanded scope in the mitsunobu reaction and retain convenient separation features

被引:44
作者
Dandapani, S [1 ]
Curran, DP [1 ]
机构
[1] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
关键词
D O I
10.1021/jo0488098
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
First generation fluorous DEAD reagent bis(perfluorohexylethyl)azo dicarboxylate (C6F13(CH2)(2)O2CN=NCO2(CH2)(2)C6F13, F-DEAD-1) has been shown to underperform relative to diisopropylazodicarboxylate in difficult Mitsunobu reactions involving hindered alcohols or less acidic pronucleophiles (phenols). Two new second generation fluorous reagents bearing propylene spacers instead of the ethylene spacers show expanded reaction scope while retaining the easy fluorous separation features. Byproducts from "half fluorous" reagent perfluorooctylpropyl tert-butyl azo dicarboxylate (C8F17(CH2)(3)O2CN=(NCO2Bu)-Bu-t, F-DEAD-2) can be removed by fluorous flash chromatography, and byproducts from bis(perfluorohexylpropyl)azo dicarboxylate (C6F13(CH2)(3)O2CN=NCO2(CH2)(3)C6F13, F-DEAD-3) can be removed by fluorous solid-phase extraction. The new reagents promise to provide general and complementary solutions for separation problems in Mitsunobu reactions without restricting reaction scope.
引用
收藏
页码:8751 / 8757
页数:7
相关论文
共 22 条
[1]   The 4-tert-butylphenyl group as a simple tag for solution phase synthesis [J].
Blodgett, J ;
Li, TY .
TETRAHEDRON LETTERS, 2004, 45 (35) :6649-6652
[2]  
Curran DP, 2001, SYNLETT, P1488
[3]   Thiol additions to acrylates by fluorous mixture synthesis: relative control of elution order in demixing by the fluorous tag and the thiol substituent [J].
Curran, DP ;
Oderaotoshi, Y .
TETRAHEDRON, 2001, 57 (24) :5243-5253
[4]   Fluorous synthesis with fewer fluorines (light fluorous synthesis): separation of tagged from untagged products by solid-phase extraction with fluorous reverse-phase silica gel [J].
Curran, DP ;
Luo, ZY .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (39) :9069-9072
[5]   Propylene spaced allyl tin reagents: A new class of fluorous tin reagents for allylations under radical and metal-catalyzed conditions [J].
Curran, DP ;
Luo, ZY ;
Degenkolb, P .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1998, 8 (17) :2403-2408
[6]  
CURRAN DP, 2004, HDB FLUOROUS CHEM, P101
[7]   Separation-friendly Mitsunobu reactions: A microcosm of recent developments in separation strategies [J].
Dandapani, S ;
Curran, DP .
CHEMISTRY-A EUROPEAN JOURNAL, 2004, 10 (13) :3130-3138
[8]   Separation tagging with cyclodextrin-binding groups: Mitsunobu reactions with bis-(2-(1-adatnantyl)ethyl) azodicarboxylate (BadEAD) and bis-(1-adamantylmethyl) azodicarboxylate (BadMAD) [J].
Dandapani, S ;
Newsome, JJ ;
Curran, DP .
TETRAHEDRON LETTERS, 2004, 45 (35) :6653-6656
[9]   Fluorous Mitsunobu reagents and reactions [J].
Dandapani, S ;
Curran, DP .
TETRAHEDRON, 2002, 58 (20) :3855-3864
[10]   Recent advances in the Mitsunobu reaction: Modified reagents and the quest for chromatography-free separation [J].
Dembinski, R .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2004, 2004 (13) :2763-2772