2,166 research outputs found
Water and Risk Assessment
Thank you for giving me the opportunity to speak to you today about carcinogens in drinking water and water quality standards. In this emotion-filled, media-hyped, chemo-phobic society in which we live, the more we spend to comply with regulations that supposedly reduce the risk of cancer, the less safe the American public seems to feel
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Transient [3,3] Cope rearrangement of 3,3-dicyano-1,5-dienes: computational analysis and 2-step synthesis of arylcycloheptanes.
A simple and modular route to arylcycloheptene scaffolds is reported. The two-step route from Knoevenagel adducts and allylic electrophiles is made possible through the design of a Cope rearrangement that utilizes a "traceless" activating group to promote an otherwise thermodynamically unfavorable transformation. Experimentally, the [3,3] rearrangement occurrs transiently at room temperature with a computed barrier of 19.5 kcal mol-1, which ultimately allows for three-component bis-allylation. Ring-closing metathesis delivers the arylcycloheptane and removes the activating group. This report describes the design and optimization of the methodology, scope and mechanistic studies, and computational analysis
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Cinchona Urea-Catalyzed Asymmetric Sulfa-Michael Reactions: The Brønsted Acid-Hydrogen Bonding Model.
This is the final version of the article. It first appeared from the American Chemical Society via http://dx.doi.org/10.1021/jacs.6b05074The cinchona alkaloid-derived urea-catalyzed asymmetric conjugate addition of aromatic thiols to cycloalkenones was studied using density functional theory (DFT). Deprotonation of the thiol gives a protonated amine that activates the electrophile by Brønsted acid catalysis, while the urea group binds the nucleophilic thiolate by hydrogen bonding. These results demonstrate the generality of the Brønsted acid-hydrogen bonding transition state (TS) model for cinchona alkaloid catalysis that we recently showed to be favored over Wynberg's widely accepted ion pair-hydrogen bonding model and represent the first detailed mechanistic study of a cinchona urea-catalyzed reaction. The conformation of the catalyst methoxy group has a strong effect on the TS, an effect overlooked in previous mechanistic studies of reactions catalyzed by cinchona alkaloids.We are grateful to The English-Speaking Union (Lindemann Trust Fellowship to M.N.G.), Girton College, Cambridge (Research Fellowship to M.N.G.) and the NSF (CHE- 1361104 to K.N.H.) for financial support. Computational resources were provided by the UCLA Institute for Digital Research and Education (IDRE) and the Extreme Science and Engineering Discovery Environment (XSEDE), which is supported by the NSF (OCI-1053575). Part of this work was performed using the Darwin Supercomputer of the University of Cambridge High Performance Computing Service (http://www. hpc.cam.ac.uk/), provided by Dell Inc. using Strategic Research Infrastructure Funding from the Higher Education Funding Council for England and funding from the Science and Technology Facilities Council
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Cinchona Alkaloid-Catalyzed Asymmetric Conjugate Additions: The Bifunctional Brønsted Acid-Hydrogen Bonding Model.
Wynberg's report from 1977 that natural cinchona alkaloids catalyze the asymmetric conjugate addition of aromatic thiols to cycloalkenones is a landmark discovery in hydrogen bonding organocatalysis. Wynberg proposed that this reaction proceeded via the formation of a thiolate-alkylammonium tight ion pair and activation of the enone electrophile by a hydrogen bond from the catalyst's hydroxyl group. This reaction model provided the mechanistic basis for understanding Wynberg's reaction and many other asymmetric transformations since. Our quantum mechanical calculations reveal a different model should be used to explain the results: the alkylammonium ion activates the enone by Brønsted acid catalysis, and the catalyst's hydroxyl group orients the thiolate nucleophile. The new model rationalizes the stereoselective outcome of Wynberg's reaction and provides a new, general model for asymmetric cinchona organocatalysis
The search for habitable worlds: 1. The viability of a starshade mission
As part of NASA's mission to explore habitable planets orbiting nearby stars,
this paper explores the detection and characterization capabilities of a 4-m
space telescope plus 50-m starshade located at the Earth-Sun L2 point, a.k.a.
the New Worlds Observer (NWO). Our calculations include the true spectral types
and distribution of stars on the sky, an iterative target selection protocol
designed to maximize efficiency based on prior detections, and realistic
mission constraints. We carry out both analytical calculations and simulated
observing runs for a wide range in exozodiacal background levels ({\epsilon} =
1 - 100 times the local zodi brightness) and overall prevalence of Earth-like
terrestrial planets ({\eta}\oplus = 0.1 - 1). We find that even without any
return visits, the NWO baseline architecture (IWA = 65 mas, limiting FPB =
4\times10-11) can achieve a 95% probability of detecting and spectrally
characterizing at least one habitable Earth-like planet, and an expectation
value of ~3 planets found, within the mission lifetime and {\Delta}V budgets,
even in the worst-case scenario ({\eta}\oplus = 0.1 and {\epsilon} = 100 zodis
for every target). This achievement requires about one year of integration time
spread over the 5 year mission, leaving the remainder of the telescope time for
UV-NIR General Astrophysics. Cost and technical feasibility considerations
point to a "sweet spot" in starshade design near a 50-m starshade effective
diameter, with 12 or 16 petals, at a distance of 70,000-100,000 km from the
telescope.Comment: Refereed and accepted to PASP, scheduled for publication in the May
2012 issue (Vol. 124, No. 915
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