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Iliohypogastric-ilioinguinal peripheral nerve block for post-Cesarean delivery analgesia decreases morphine use but not opioid-related side effects
PurposeTo examine if ilioinguinal-iliohypogastric nerve block could reduce the need for post-Cesarean delivery morphine analgesia and thus reduce the incidence of opioid relatedExpand
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Forest Roads Facilitate the Spread of Invasive Plants
Abstract The distribution and abundance of invasive species can be strongly influenced by habitat suitability and by corridors that facilitate dispersal. We synthesize results from a large-scaleExpand
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Double-Crop Soybean Leaf Area and Yield Responses to Mid-Atlantic Soils and Cropping Systems
Double-crop soybean (Glycine max L.) often yields less than full-season soybean, due in part to decreased leaf area development. Information is lacking on the effect of cropping system andExpand
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Evaluation of potentially labile soil organic carbon and nitrogen fractionation procedures
Abstract Particulate organic matter (POM) and light fraction (LF) organic matter are potentially labile (active) fractions of soil organic matter (SOM) that have been shown to be indicators ofExpand
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Effects of Twin-Row Spacing on Corn Silage Growth Development and Yield in the Shenandoah Valley
Virginia Cooperative Extension programs and employment are open to all, regardless of race, color, national origin, sex, religion, age, disability, political beliefs, sexual orientation, or maritalExpand
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Determination and Manipulation of Leaf Area Index to Facilitate Site-Specific Management of Double-Crop Soybean in the Mid-Atlantic, U.S.A.
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Commercial Route Research and Development for SGLT2 Inhibitor Candidate Ertugliflozin
A practical synthesis of SGLT2 inhibitor candidate ertugliflozin (1) has been developed for potential commercial application. The highly telescoped process involves only three intermediate isolationsExpand
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DBU catalysis of N,N'-carbonyldiimidazole-mediated amidations.
1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) has been found to catalyze the amidation of acyl imidazoles. The rate acceleration is especially evident with traditionally unreactive, electron-deficientExpand
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Cross-Coupling Methods for the Large-Scale Preparation of an Imidazole−Thienopyridine: Synthesis of [2-(3-Methyl-3H-imidazol-4-yl)- thieno[3,2-b]pyridin-7-yl]-(2-methyl-1H-indol-5-yl)-amine
The multihundred-gram synthesis of [2-(3-methyl-3H-imidazol-4-yl)-thieno[3,2-b]pyridin-7-yl]-(2-methyl-1H-indol-5-yl)-amine (1) is described utilizing a Stille cross-coupling of an iodothienopyridineExpand
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