SOLUABLE POLYMER SUPPORTS FOR ORGANIC SYNTHESIS
SOLUABLE POLYMER SUPPORTS FOR ORGANIC SYNTHESIS
批准号:
6386713
负责人:
Kim Janda
金额:
$26.36万
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-09-30 至 2003-09-29
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION: Polymer-supported chemistry has undergone a dramatic revival.
The primary impetus has been the development of "small-molecule"
combinatorial technology for drug discover. However, despite the
popularity and successes of resins such as cross-linked polystyrene,
insoluble polymers have a number of drawbacks for use in organic
synthesis. There can be detrimental effects on reaction rates,
selectivities and yields. and spectroscopic analyses are hampered.
Furthermore, solid supports are not particularly effective in water.
Hence, a number of currently valuable biocatalytic transformations can not
be efficiently performed. A soluble support would allow the expectations
and methods of traditional solution chemistry, while affording the
benefits of the polymer phase.
The investigators have embarked on a multifaceted program to develop the
utility of soluble polymers in organic synthesis. This includes the
discovery of unique soluble polymers for synthetic applications.
Significantly a method coined "parallel polymer synthesis" will provide
access to a large number of novel materials. Finally, examples are
presented that highlight the power of soluble technology in the synthesis
of complex molecules such as prostanoids and chiral building blocks. This
will include library construction and the implementation of a polymer-
supported technique termed the "oscillating liquid phase" made possible by
the variance in physical properties of our new co-polymers. It is
anticipated that soluble-polymer supports will finding increasing utility
in synthesis in the coming years.
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DOI:
10.1021/jo016362m
发表时间:
2002-03
期刊:
The Journal of organic chemistry
影响因子:
--
作者:
[C. Spanka;B. Clapham;K. Janda]
通讯作者:
C. Spanka;B. Clapham;K. Janda
Developing soluble polymers for high-throughput synthetic chemistry.
开发用于高通量合成化学的可溶性聚合物。
DOI:
10.2174/1386207024607239
发表时间:
2002
期刊:
Combinatorial chemistry & high throughput screening
影响因子:
1.8
作者:
[Spanka,Carsten, WentworthJr,Paul, Janda,KimD]
通讯作者:
Janda,KimD
Exploring the scope of poly(ethylene glycol) (PEG) as a soluble polymer matrix for the Stille cross-coupling reaction.
探索聚乙二醇 (PEG) 作为 Stille 交叉偶联反应的可溶性聚合物基质的范围。
DOI:
10.1021/cc990052o
发表时间:
1999
期刊:
Journal of combinatorial chemistry.
影响因子:
--
作者:
[Sieber,F, WentworthJr,P, Janda,KD]
通讯作者:
Janda,KD
A polymer-supported proline-based diamine catalyst for the kinetic resolution of racemic secondary alcohols.
一种聚合物负载的脯氨酸基二胺催化剂,用于动力学拆分外消旋仲醇。
DOI:
10.1021/jo0013610
发表时间:
2001
期刊:
The Journal of organic chemistry
影响因子:
--
作者:
[Clapham,B, Cho,CW, Janda,KD]
通讯作者:
Janda,KD
Preparation of soluble and insoluble polymer supported IBX reagents.
可溶性和不溶性聚合物支持的 IBX 试剂的制备。
DOI:
10.1016/s0960-894x(02)00264-0
发表时间:
2002
期刊:
Bioorganic & medicinal chemistry letters
影响因子:
2.7
作者:
[Reed,NealN, Delgado,Mercedes, Hereford,Kristina, Clapham,Bruce, Janda,KimD]
通讯作者:
Janda,KimD
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High-Throughput Screen for the Oncoprotein MYC
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批准号:10657663
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High-Throughput Screen for the Oncoprotein MYC
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批准号:10436377
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财政年份:2021
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Covalent Inhibition as a Method to Counteract Botulinum Intoxication
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Covalent Inhibition as a Method to Counteract Botulinum Intoxication
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资助金额:$63.46万
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财政年份:2020
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依托单位:
Covalent Inhibition as a Method to Counteract Botulinum Intoxication
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资助金额:$69.27万
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依托单位:
"PRODUCTION AND DISTRIBUTION OF INVESTIGATIONAL GHRELIN VACCINES-- GHRELIN VACCINES AGAINST RAT HORMONE". TASK ORDER 5. 09/21/2019-12/31/2020.
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项目类别:
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资助金额:$11.62万
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依托单位:
Immunotherapy to Counteract Lethal Doses of Carfentanil
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项目类别:
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IGF::OT::IGF:The Scripps Research Institute. Task Order 3 (HHSN275201500006I/HHSN27500003)."Production and Distribution of Investigational Ghrelin Vaccines--Ghrelin Vaccine Against Rat Hormone. 09/21/
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资助金额:$12.24万
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依托单位:
A Multidisciplinary Approach for the Treatment of Botulinum Intoxication
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Enzympharmacotherapy for attenuating nicotine's psychoactive effects
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资助金额:$62.82万
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财政年份:2016
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Using Allosteric Inhibition as a Means to Ablate Botulinum Neurotoxin Protease
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资助金额:$24.06万
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Approaches to Counteract the Harmful Effects of Synthetic Opioid Designer Drugs
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依托单位:
海外基金