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MBHManaged Behavioral Health (various organizations)
MBHMini-Black Hole (physics)
MBHMaschinenfabrik Berthold Hermle (German engineering works company)
MBHMorita-Baylis-Hillman (chemical reaction)
MBHMaintenance-by-the-Hour (Singapore Technologies Aerospace)
MBHMexico Boutique Hotels (est. 1999)
MBHMann Bradley Hughes (authors of paper on climate change)
MBHMedial Basal Hypothalamus
MBHMissouri Baptist Hospital (St. Louis, MO)
MBHMobile Backhaul (Metro Ethernet Forum)
MBHMonex Beans Holdings, Inc. (Japan)
MBHMadeline and the Bad Hat (Ludwig Bemelmans book)
MBHMicroscopic Black Hole
MBHMy Brain Hurts
MBHModern Blues Harmonica
MBHMessage Board Help
MBHMit Beschrnkter Haftung (German: With Limited Liability)
MBHMobile Block Hessian (molecular vibrational node analysis)
MBHMr. Bean's Holiday (movie)
MBHMain Boiler House
MBHMan Bytes Hollywood
MBHThousand BTU's Per Hour (means cost guide)
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References in periodicals archive ?
The product of this reaction is known as Ruhemann's purple (Rp) [3-4].The literature review shows that study of reactions of ninhydrin is a subject of more interest and some of the useful reactions such as amidoalkylation[5], Knoevenagel condensation [6], oxidation [7,8], reduction [9,10], reaction with enols and aromatic compounds [11], synthesis of heterocyclic compounds [12], Friedel-Crafts type reaction [13-16], Kolbe-Schmitt [17], Passerini [18], Wittig [19] and Morita-Baylis-Hillman [20] have been investigated in this area.
Kim, A Practical Synthesis of Morita-Baylis-Hillman Adducts of Aryl Vinyl Ketones Catalyzed by a Proton Donor, Bull.
Bharadwaj, "Intramolecular Morita-Baylis-Hillman and Rauhut-Currier reactions.
Shi, "The Morita-Baylis-Hillman (MBH) and Hetero-MBH Reactions," Comprehensive Enantioselective Organocatalysis: Catalysts, Reactions, and Applications, vol.
Takizawa, 6.9 C-C Bond Formation: (aza) Morita-Baylis-Hillman Reaction Comprehensive Chirality, vol.
de Oliveira et al., "Synthesis and activity of novel homodimers of Morita-Baylis-Hillman adducts against Leishmania donovani: A twin drug approach," Bioorganic & Medicinal Chemistry Letters, vol.
Batra, "Applications of morita-baylis-hillman reaction to the synthesis of natural products and drug molecules," Current Organic Chemistry, vol.
Vasconcellos, "Morita-Baylis-Hillman adducts: Biological activities and potentialities to the discovery of new cheaper drugs," Bioorganic & Medicinal Chemistry, vol.
Another paper showed the Morita-Baylis-Hillman adducts (MBHA) are a novel group of synthetic molecules that act as anti-inflammatory by modulating inflammatory mediator expression in RAW264.7 macrophages and adenocarcinoma colorectal human HT-29 cells.
The Morita-Baylis-Hillman adducts (MBHA) have been described as anticancer compounds [20-22].
Marques-Santos, "Antimitotic activity on sea urchin embryonic cells of seven antiparasitic Morita-Baylis-Hillman adducts: a potential new class of anticancer drugs," Medicinal Chemistry, vol.
Bomfim et al., "Synthesis, cytotoxic activity on leukemia cell lines and quantitative structure-activity relationships (QSAR) studies of Morita-Baylis-Hillman adducts," Medicinal Chemistry, vol.