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Synthesis of the C1-C15 fragment of elaiolide
被引:1
|
作者
:
Singh, Yadav Jhillu
论文数:
0
引用数:
0
h-index:
0
机构:
Indian Inst Chem Technol, Nat Prod Chem Div, Hyderabad 500007, Andhra Pradesh, India
Indian Inst Chem Technol, Nat Prod Chem Div, Hyderabad 500007, Andhra Pradesh, India
Singh, Yadav Jhillu
[
1
]
Yarrapothu, Gangadhara Rao
论文数:
0
引用数:
0
h-index:
0
机构:
Indian Inst Chem Technol, Nat Prod Chem Div, Hyderabad 500007, Andhra Pradesh, India
Indian Inst Chem Technol, Nat Prod Chem Div, Hyderabad 500007, Andhra Pradesh, India
Yarrapothu, Gangadhara Rao
[
1
]
Vemula, Rajender
论文数:
0
引用数:
0
h-index:
0
机构:
Indian Inst Chem Technol, Nat Prod Chem Div, Hyderabad 500007, Andhra Pradesh, India
Indian Inst Chem Technol, Nat Prod Chem Div, Hyderabad 500007, Andhra Pradesh, India
Vemula, Rajender
[
1
]
机构
:
[1]
Indian Inst Chem Technol, Nat Prod Chem Div, Hyderabad 500007, Andhra Pradesh, India
来源
:
RSC ADVANCES
|
2013年
/ 3卷
/ 01期
关键词
:
FORMAL TOTAL-SYNTHESIS;
ENANTIOSELECTIVE SYNTHESIS;
ALDOL REACTIONS;
STEREOSELECTIVE-SYNTHESIS;
SECONDARY METABOLITES;
ELAIOPHYLIN;
AZALOMYCINS;
(+)-11,11-DI-O-METHYLELAIOPHYLIDENE;
MACRODIOLIDE;
ESTERS;
D O I
:
10.1039/c2ra22122e
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
The synthesis of the C1-C15 fragment of elaiolide was achieved by successfully utilizing the desymmetrization strategy, zirconium catalyzed C-C bond formation and double stereodifferentiating aldol reactions.
引用
收藏
页码:55 / 58
页数:4
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