A NOVEL TETRAHYDROFURAN DERIVATIVE VIA A TERTIARY KETOL-TYPE REARRANGEMENT

被引：14

作者：

DREWES, SE

EMSLIE, ND

FIELD, JS

KHAN, AA

RAMESAR, NS

机构：

[1] Department of Chemistry, University of Natal, Pietermaritzburg

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 07期

关键词：

D O I：

10.1016/S0040-4039(00)77529-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Hexahydro-3a,7a-dihydroxy-3,7,7-trimethyl-2-phenyl-4H-furo[3,2c]pyran-4-one 6 has been obtained from the reaction between tetrahydro-4,4-dimethyl-2-oxo-3-furanyl propanoate 4, benzaldehyde and base. The product is the result of a modified benzilic acid rearrangement.

引用

页码：1205 / 1208

页数：4

共 21 条

[11] DREWES SE, IN PRESS SYNTH COMMU
[12] DREWES SE, UNPUB
[13] DRREWES DE, 1990, CHEM BER, V123, P2455
[14] SELECTIVE MONO AND BISCONDENSATIONS OF DIALDEHYDES WITH METHYLACRYLATE
FORT, Y
BERTHE, MC
CAUBERE, P
[J]. SYNTHETIC COMMUNICATIONS, 1992, 22 (09) : 1265 - 1275
[15] ASYMMETRIC INDUCTION IN THE BAYLIS-HILLMAN REACTION
GILBERT, A
HERITAGE, TW
ISAACS, NS
[J]. TETRAHEDRON-ASYMMETRY, 1991, 2 (10) : 969 - 972
[16] LODER JW, 1977, HETEROCYCLES, V7, P113
[17] STEREOSELECTIVE ADDITION OF METHYL ACRYLATE TO ALPHA-AMINO ALDEHYDES
MANICKUM, T
ROOS, G
[J]. SYNTHETIC COMMUNICATIONS, 1991, 21 (22) : 2269 - 2274
[18] DABCO-CATALYZED COUPLING OF ALDEHYDES WITH ACTIVATED DOUBLE-BONDS .6. STEREOSELECTIVE GENERATION AND FACILE DIMERIZATION OF (E)-2-METHYLENE-3-ALKENOIC ACID-ESTERS
POLY, W
SCHOMBURG, D
HOFFMANN, HMR
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (16) : 3701 - 3710
[19] AN INTRAMOLECULAR BAYLIS-HILLMAN REACTION
ROTH, F
GYGAX, P
FRATER, G
[J]. TETRAHEDRON LETTERS, 1992, 33 (08) : 1045 - 1048
[20] BENZILIC ACID AND RELATED REARRANGEMENTS
SELMAN, S
EASTHAM, JF
[J]. QUARTERLY REVIEWS, 1960, 14 (03): : 221 - 235

← 1 2 3 →