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Chapter 8 Alkenes and Alkynes II
Chapter 8 Alkenes and Alkynes II

... The reaction of alkenes with dilute aqueous acid leads to Markovnikov addition of water ...
CrO3/Al2O3: Rapid oxidation of alcohols to carbonyl compounds in
CrO3/Al2O3: Rapid oxidation of alcohols to carbonyl compounds in

Organic Chemistry - Snow College | It's SNOWing
Organic Chemistry - Snow College | It's SNOWing

... • have lower boiling points and are less soluble in water than alcohols of comparable MW ...
Exam III
Exam III

... stereospecific reactions, be able to show the structures for the alkene reactants. -given the structures of the reactants and the products be able to state whether a reaction is syn- or anti-. ...
NUCLEOPHILIC SUBSTITUTION & ELIMINATION ON Csp 3
NUCLEOPHILIC SUBSTITUTION & ELIMINATION ON Csp 3

... Uses of SN2 in drug design an example: Ciguatera – a GI and a neuropathological condition caused by a natural toxin, ciguatoxin, found in certain tropical fish Treating ciguatera required using toxin to study its mode of action; as toxin is difficult to isolate it had to be prepared de novo – using ...
3.8 Aldehydes and ketones
3.8 Aldehydes and ketones

... In practise, KCN is added. This is because HCN is a weak acid (partially dissociates) giving a low [CN-] ...
Organometallic Chemistry
Organometallic Chemistry

... 1973 – Commercial synthesis of L-Dopa (Parkinsonʼs drug) ...
Synthesis of Novel Steroid-Peptoid Hybrid Macrocycles by
Synthesis of Novel Steroid-Peptoid Hybrid Macrocycles by

... synthetic receptor is not only a result of the presence of the proper recognition elements, but also of their relative disposition in space and the three-dimensional shape of the overall interaction [5]. In this sense, molecules such as steroids with well-defined, preorganized architectures are amen ...
Reactions of Alcohols - John Carroll University
Reactions of Alcohols - John Carroll University

... Many reagents are available to oxidize a simple secondary alcohol to a ketone. For a laboratory synthesis, however, dehydrogenation is not practical, and cost is not as large a factor as it would be in industry. Most labs would have chromium trioxide or sodium dichromate available, and the chromic a ...
Chapter 24. Amines
Chapter 24. Amines

... para is blocked ...
Chapter 24. Amines - Houston Community College System
Chapter 24. Amines - Houston Community College System

... para is blocked ...
Materials Chemistry Prof. S. Sunder Manoharan Department of
Materials Chemistry Prof. S. Sunder Manoharan Department of

... approach to solid state synthesis is the direct reaction of solids which is not very, very intricate it does not call for very stringent application, but then once you get a feel for it is easier for to make many materials. Therefore, these are grouped under 1 direct reaction of solids precursor met ...
File
File

... position decreases the electron density in the O−H bond. As a result, it is easier to lose a proton. Also, the o-nitrophenoxide ion formed after the loss of protons is stabilized by resonance. Hence, ortho nitrophenol is a stronger acid. On the other hand, methoxy group is an electron-releasing grou ...
Learning Guide for Chapter 16
Learning Guide for Chapter 16

... esters - also have C=O band alcohols - also have OH band anhydrides - also have 2 C=O bands NMR Spectra of Ethers What chemical shift are the H's next to the O in an ether? 3-4 ppm H ...
Ruthenium(II) Complexes Bearing a Pyridyl-Supported Pyrazolyl
Ruthenium(II) Complexes Bearing a Pyridyl-Supported Pyrazolyl

... for the ketone within 4 h (Table 1, entry 1). Under the same conditions, complexes 7 and 8 nearly exhibited the same catalytic activity, reaching 97-98% conversions for acetophenone over a period of 2 h and 97-98% conversions for 4-bromoacetophenone with a final TOF up to 1940 h-1 within 15 min. Pre ...
Ch 10 Haloalkanes n haloarenes
Ch 10 Haloalkanes n haloarenes

... Ans13 .A mixtures of 2 enantiomers. Ans 14 .DDT is used as an insecticide and Freon is used as refrigerant in refrigerator and air conditioner. Ans 15.Chlorination of Benzene in presence of AlCl3. Ans 16.enantiomers rotate the plane of polarized light either towards right or towards left. Ans17.1- b ...
NACOS with Nitroxy Radicals as Cocatalysts: An Efficient, Green
NACOS with Nitroxy Radicals as Cocatalysts: An Efficient, Green

... alcohols. Notably, Hu’s group has recently reported a series of metal-free aerobic alcohol oxidation protocols (TEMPO/Br2/NaNO2 system, and its modified versions). Those methods provided great advances in the field of non-metallic aerobic oxidation. However, they required expensive teflon-lined auto ...
Integration of chemical catalysis with extractive fermentation to
Integration of chemical catalysis with extractive fermentation to

... undecan-6-one. Yields based on acetone. Reaction conditions: acetone (2.3 mmol), ethanol (1 mmol), butanol (3.7 mmol), 5% Pd/C (0.01 mmol), K3PO4 (3 mmol), toluene (1.5 ml), temperature (x axis), 20 h. b, Effect of K3PO4 loading on product yields. K3PO4 loading is represented as molar equivalents wi ...
unit 6 alcohols
unit 6 alcohols

...  Esters: Now the LG is RO-, not usually considered “good,” but the reaction takes place by nucleophilic acyl substitution, not by SN2. In this mechanism, RO- leaving is exothermic and therefore favorable. ...
Staff demonstrating hours for level-3 Inorganic Lab
Staff demonstrating hours for level-3 Inorganic Lab

... EXAMPLE trans-(Et3P)2PtHCl + C2H4  trans-(Et3P)2PtCl(C2H5) In this example the resulting ethyl complex is stable because the d 8 platinum Pt(2+) atom strongly prefers square-planar geometry. A related route is insertion of a carbene into a TM-H bond EXAMPLE CpMo(CO)3H + CH2N2  CpMo(CO)3(CH3) CH2N2 ...
Sn1 and Sn2 Chemtivity
Sn1 and Sn2 Chemtivity

... 3. How is this different from the SN2 mechanism? ...
LECTURE PPT: Chapter 8
LECTURE PPT: Chapter 8

... • MTBE (methyl tertiary butyl ether, CH3OC(CH3)3) was the additive of choice by the oil companies. • MTBE is a compound that does not biodegrade readily. • MTBE made its way into drinking water through gasoline spills at gas stations, from boat motors, and from leaking underground storage tanks. • E ...
Handbook for the Lab Course Organic Chemistry I
Handbook for the Lab Course Organic Chemistry I

Chem 30CL-Lecture 12.. - UCLA Chemistry and Biochemistry
Chem 30CL-Lecture 12.. - UCLA Chemistry and Biochemistry

...  Acid removes the BOC group (CO2, tert.-BuOH)  Pd-C/H2 removes the benzyl group as toluene ...
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Discodermolide



(+)-Discodermolide is a polyketide natural product found to stabilize microtubule. (+)-discodermolide was isolated by Gunasekera and his co-workers at the Harbor Branch Oceanographic Institute from the deep-sea sponge Discodermia dissoluta in 1990. (+)-Discodermolide was found to be a potent inhibitor of tumor cell growth in several MDR cancer cell lines. (+)-discodermolide also shows some unique characters, including a linear backbone structure, immunosuppressive properties both in vitro and in vivo, potent induction of an accelerated senescence phenotype, and synergistic antiproliferative activity in combination with paclitaxel. Discodermolide was recognized as one of the most potent natural promoters of tubulin assembly. A large number of efforts toward the total synthesis of (+)-discodermolide were directed by its interesting biological activities and extreme scarcity of natural sources (0.002% w/w from frozen marine sponge). The compound supply necessary for complete clinical trials cannot be met by harvesting, isolation, and purification. As of 2005, attempts at synthesis or semi-synthesis by fermentation have proven unsuccessful. As a result, all discodermolide used in preclinical studies and clinical trials has come from large-scale total synthesis.
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