HIGH DIASTEREOSELECTIVITY IN LEWIS ACID MEDIATED ALDOL CONDENSATIONS USING THIOESTER SILYL KETENE ACETALS

被引：30

作者：

GENNARI, C

BERNARDI, A

CARDANI, S

SCOLASTICO, C

机构：

来源：

关键词：

D O I：

10.1016/S0040-4039(00)89140-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：797 / 800

页数：4

共 19 条

[1] THE ALPHA-HYDROGEN REACTIVITY OF THIOLESTERS
CRONYN, MW
CHANG, MP
WALL, RA
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (11) : 3031 - 3034
[2] DUBOIS JE, 1984, TETRAHEDRON LETT, P4655
[3] STEREOSELECTIVE ALDOL CONDENSATIONS VIA BORON ENOLATES
EVANS, DA
NELSON, JV
VOGEL, E
TABER, TR
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (11) : 3099 - 3111
[4] EVANS DA, 1980, TETRAHEDRON LETT, P3975
[5] EVANS DA, 1982, TOP STEREOCHEM, V13, P1, DOI DOI 10.1002/9780470147221.CHL
[6] GENNARI C, TETRAHEDRON
[7] GENNARI C, 1984, TETRAHEDRON LETT, P2283
[8] ACYCLIC STEREOSELECTION .16. HIGH DIASTEREOFACIAL SELECTIVITY IN LEWIS ACID MEDIATED ADDITIONS OF ENOLSILANES TO CHIRAL ALDEHYDES
HEATHCOCK, CH
FLIPPIN, LA
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (06) : 1667 - 1668
[9] HEATHCOCK CH, 1984, ALDOL ADDITION REACT, V3, P136
[10] HIRAMA M, 1979, TETRAHEDRON LETT, P2225