Free radical allyl transfers utilizing soluble non-cross-linked polystyrene and carbohydrate scaffold supports

被引:35
作者
Enholm, EJ [1 ]
Gallagher, ME [1 ]
Jiang, SJ [1 ]
Batson, WA [1 ]
机构
[1] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
关键词
D O I
10.1021/ol006449e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[GRAPHICS] Free radical allylations were studied using (1) soluble non-cross-linked polystyrene supports, (2) carbohydrate scaffolds, and (3) a combination of both synthetic motifs, Allylations on these custom designer supports provide easily purified products, free of tin residues. A D-xylose carbohydrate scaffold bearing a bromoester was used for a diastereoselective allyl tin transfer thermally at 80 degrees C and with Lewis acids. This is the first example of a diastereoselective radical reaction directed by a removable polymer-supported carbohydrate auxiliary.
引用
收藏
页码:3355 / 3357
页数:3
相关论文
共 25 条
[1]  
Berteina S, 1999, SYNLETT, P1121
[2]  
Berteina S, 1998, SYNLETT, P1231
[3]  
Brown AR, 1998, SYNLETT, P817
[4]   Solid-phase intermolecular radical reactions 1. Sulfonyl radical addition to isolated alkenes and alkynes [J].
Caddick, S ;
Hamza, D ;
Wadman, SN .
TETRAHEDRON LETTERS, 1999, 40 (40) :7285-7288
[5]   An allylstannane reagent on non-cross-linked polystyrene support [J].
Enholm, EJ ;
Gallagher, ME ;
Moran, KM ;
Lombardi, JS ;
Schulte, JP .
ORGANIC LETTERS, 1999, 1 (05) :689-691
[6]   Convenient catalytic free radical reductions of alkyl halides using an organotin reagent on non-cross-linked polystyrene support [J].
Enholm, EJ ;
Schulte, JP .
ORGANIC LETTERS, 1999, 1 (08) :1275-1277
[7]   Highly diastereoselective Diels-Alder reactions using a fructose diacetonide chiral scaffold [J].
Enholm, EJ ;
Jiang, SJ .
JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (15) :4756-4758
[8]  
Gordon K, 1999, J CHEM TECHNOL BIOT, V74, P835, DOI 10.1002/(SICI)1097-4660(199909)74:9<835::AID-JCTB130>3.3.CO
[9]  
2-Q
[10]  
Jeon GH, 2000, SYNLETT, P128