Synthetic approaches to homogynolides A and B
摘要：
A four step, efficient and general methodology for the conversion of a cyclic ketone into the corresponding alpha-spiro-beta-methylene-gamma-butyrolactone, the key structural feature present in tricyclic sesquiterpenes bakkanes, has been developed employing a regiospecific 5-exo dig radical cyclisation reaction as the key step. The methodology has been extended to the total synthesis of bakkanes including homogynolide-B and chiral homogynolide-A.
展开
关键词：
Radical chain reactions Organic-synthesis Stereoselective synthesis Cyclization Bakkanes Strategy Alpina Design
DOI：
10.1351/pac199668030699
被引量：
年份：
1996
De Gruyter
国家科技图书文献中心
(权威机构)
doi.org
掌桥科研
dx.doi.org
查看更多
ResearchGate
Citeseer
EBSCO
Citeseer
(全网免费下载)
eprints.iisc.ernet.in
list.iupac.org
(全网免费下载)
media.iupac.org
(全网免费下载)
moureu.iupac.org
(全网免费下载)
iupac.org
(全网免费下载)
old.iupac.org
(全网免费下载)
mendeley.com
iupac.org
(全网免费下载)
iupac.org
repository.ias.ac.in
core.ac.uk
学术范
学术范
(全网免费下载)
Citeseer
(全网免费下载)
media.iupac.org
(全网免费下载)
iupac.org
(全网免费下载)
moureu.iupac.org
(全网免费下载)
old.iupac.org
(全网免费下载)
iupac.org
(全网免费下载)
list.iupac.org
(全网免费下载)
学术范
(全网免费下载)
通过文献互助平台发起求助，成功后即可免费获取论文全文。
相似文献
参考文献
引证文献
辅助模式
引用
文献可以批量引用啦~
欢迎点我试用！
