SYNTHESIS OF (+/-)-(ALPHA)-CUPARENONES VIA HYDROCARBONYLATING CYCLIZATION OF 1,4-DIENES

被引：11

作者：

EILBRACHT, P

BALSS, E

ACKER, M

机构：

来源：

TETRAHEDRON LETTERS | 1984年 / 25卷 / 11期

关键词：

D O I：

10.1016/S0040-4039(01)91541-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

收藏

页码：1131 / 1132

页数：2

相关论文

共 10 条

[1] CHAKRAVA.J, 1969, INDIAN J CHEM, V7, P215
[2] A HYBRID BIRCH-CLAISEN METHODOLOGY FOR ARYLATION AT ALLYLIC TERMINI - SYNTHESIS OF (+/-)-HERBERTENE
CHANDRASEKARAN, S
TURNER, JV
[J]. TETRAHEDRON LETTERS, 1982, 23 (37) : 3799 - 3802
[3] ALKYLSUBSTITUTED CYCLOPENTANONES VIA HYDROCARBONYLATING CYCLIZATION OF 1,4-PENTADIENE SYSTEMS MEDIATED BY METAL-CARBONYLS
EILBRACHT, P
ACKER, M
TOTZAUER, W
[J]. CHEMISCHE BERICHTE-RECUEIL, 1983, 116 (01): : 238 - 242
[4] AN ACCIDENTAL SYNTHESIS OF (+/-)-HERBERTENE
FRATER, G
[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1982, (09) : 521 - 522
[5] EFFICIENT REGIOSELECTIVE SYNTHESES OF ALPHA-CUPARENONES AND BETA-CUPARENONES - A NEW APPROACH FOR THE CONSTRUCTION OF THE CYCLOPENTANE RING
HALAZY, S
ZUTTERMAN, F
KRIEF, A
[J]. TETRAHEDRON LETTERS, 1982, 23 (42) : 4385 - 4388
[6] HAYAKAWA Y, 1978, TETRAHEDRON LETT, P993
[7] SYNTHESIS OF DL-3-HYDROXYCUPARENE BY A CLAISEN REARRANGEMENT OF ALLYL ARYL ETHER
INOUYE, Y
INOMATA, S
ISHIHARA, Y
KAKISAWA, H
[J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1982, 55 (01) : 208 - 211
[8] LEVIVEREND ML, 1982, J CHEM SOC CHEM COMM, P866
[9] DIRECTING EFFECT OF NEIGHBORING AROMATIC-GROUPS ON THE REGIOCHEMISTRY OF FORMATION AND ON THE STEREOCHEMISTRY OF ALKYLATION AND BROMINATION OF KETONE LITHIUM ENOLATES - EVIDENCE FOR LITHIUM-ARENE PI-COORDINATION AND FOR A DRAMATIC EFFECT OF EVEN SMALL AMOUNTS OF COPPER(I) IN CONTROLLING STEREOCHEMISTRY AND IN LIMITING POLYALKYLATIONT
POSNER, GH
LENTZ, CM
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1979, 101 (04) : 934 - 946
[10] DIRECT GEMINAL DIMETHYLATION OF KETONES USING DIMETHYLTITANIUM DICHLORIDE
REETZ, MT
WESTERMANN, J
STEINBACH, R
[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1981, (05) : 237 - 239