Synthesis of a new spiroacetal based herbicide

被引：4

作者：

Brimble, MA ^{[1
]}

Johnston, AD ^{[1
]}

Furneaux, RH ^{[1
]}

机构：

[1] IND RES LTD,PETONE,NEW ZEALAND

来源：

TETRAHEDRON LETTERS | 1997年 / 38卷 / 20期

基金：

澳大利亚研究理事会;

关键词：

D O I：

10.1016/S0040-4039(97)00671-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[3R*, 5S*, 6S*]-3-Benzyloxy-5-methoxy-1,7-dioxaspiro[5.5]undecane 3 and [3R*, 5S*, 6S*]-3-methoxy-5-benzyloxy-1,7-dioxaspiro[5.5]undecane 4 were prepared making use of a base induced rearrangement of a 4,5-epoxy-1,7-dioxaspiro[5.5]undecane. (C) 1997 Elsevier Science Ltd.

引用

页码：3591 / 3594

页数：4

共 9 条

[1] 2-BENZYLOXY-6,8-DIOXABICYCLO[3.2.1]OCTANES - NEW CARBOHYDRATE-DERIVED HERBICIDES
BLATTNER, R
FURNEAUX, RH
MASON, JM
TYLER, PC
[J]. PESTICIDE SCIENCE, 1991, 31 (04): : 419 - 435
[2] SYNTHETIC ROUTES TO TETRAHYDROFURAN, TETRAHYDROPYRAN, AND SPIROKETAL UNITS OF POLYETHER ANTIBIOTICS AND A SURVEY OF SPIROKETALS OF OTHER NATURAL-PRODUCTS
BOIVIN, TLB
[J]. TETRAHEDRON, 1987, 43 (15) : 3309 - 3362
[3] ALLYLIC FUNCTIONALIZATION OF THE 1,7-DIOXASPIRO[5.5]UNDEC-4-ENE AND 1,6,8-TRIOXADISPIRO[4.1.5.3]PENTADEC-13-ENE RING-SYSTEMS
BRIMBLE, MA
EDMONDS, MK
WILLIAMS, GM
[J]. TETRAHEDRON, 1992, 48 (31) : 6455 - 6466
[4] Deslongchamps P., 1983, Stereoelectronic Effects in Organic Chemistry
[5] SYNTHESIS AND THERMAL CHEMISTRY OF ISOLEVOGLUCOSENONE
FURNEAUX, RH
GAINSFORD, GJ
SHAFIZADEH, F
STEVENSON, TT
[J]. CARBOHYDRATE RESEARCH, 1986, 146 (01) : 113 - 128
[6] KLUGE AF, 1986, HETEROCYCLES, V24, P1699
[7] Payne SB., 1983, Patent No. 81893
[8] CHEMISTRY OF SPIROKETALS
PERRON, F
ALBIZATI, KF
[J]. CHEMICAL REVIEWS, 1989, 89 (07) : 1617 - 1661
[9] SAMMES PG, 1983, J CHEM SOC P1, P2727

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