1,880,123 research outputs found
Lucas' B&B Restaurant
No full textRecto: [imprinted] Lucas' B & B Restaurant Serving Dallas Since 1911, 3520 Oak Lawn Avenue, Dallas, Texas. Verso: [imprinted] Lucas B&B Restaurant. 15,342 F. Pub. by Crescent Adv., N.Y., N.Y. [descriptive text not transcribed]
[Stammbuch B. B.]
No full text[STAMMBUCH B. B.]
[Stammbuch B. B.] ( - )
Cover ( - )
Exlibris: Hans Stula ( - )
Einträge, S. 1 - 19 (1)
Einträge, S. 21 - 49 (21)
Einträge, S. 55 - 85 (55)
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Boston, Massachusetts 1868
No full textShows wards and railroads; Relief shown by hachures; Oriented with north to the upper right; Inset: East Boston; "Entered according to act of Congress in the year 1868 by B.B. Russell in the clerk's office of the District Court of Mass." Held at the American Geographical Society Library, University of Wisconsin Milwaukee.Color
B. B. King
No full textHandy Awards; Prince Gabe, Phineas Newbern Jr., B. B. Kinghttps://egrove.olemiss.edu/bluesphoto_one/1296/thumbnail.jp
<b>Site Suitability for turmeric production in India </b><b></b><b>—</b><b> A GIS interpretation</b>
No full text142-147India has 1,49,410 hectares area under turmeric cultivation with a total
annual production of 527,960 tonnes. The compound growth rate of turmeric area
is 6.30 and production is 3.37 when comparing 2000 levels over those of 1970. It
shows that the increase in area is not having significant effect over the
production rate. In the present paper the suitability maps and area productivity
graphs are given to show, the position of turmeric in the important turmeric
growing states. It was found that site suitability is an important factor to
determine the productivity of the crop. A highly suitable location may not
result in larger yields than suitable or marginally suitable areas. Suitability
maps are useful to determine areas which will have the greatest success for
growing a particular crop in a region
<b>Phyto-pharmacology of <i>Moringa oleifera</i></b><b> Lam. </b><b>— </b><b>An overview</b>
No full text347-353Moringa
oleifera Lam. is a
small or medium-sized tree, about 10 m high, cultivated throughout India. It is
a multipurpose tree, used as vegetable, spice, a source of cooking and cosmetic
oil and as a medicinal plant. It is reported to contain alkaloids, flavonoids,
anthocyanins, proanthocyanidins and cinnamates. It possesses anti-inflammatory,
antioxidant, antimicrobial, antihyperlipidaemic, antifertility, anticancer,
antihepatotoxic and antiulcer activities. Further, activity guided phytochemical
and phytoanalytical studies may lead to development of novel agents to be used
in various disorders. An overview of chemical constituents present in the plant
and their pharmacological actions are given in the present paper
[Memo to W. P. Gannaway by B. B. Norris, December 5, 1963]
No full textPhotocopy of an office memorandum addressed to Captain W. P. Gannaway of the Special Service Bureau in Dallas, Texas. In the memo, detective B. B. Norris states that FBI agents A. J. Zimmerman and Joseph J. Peggs came into the office to look at the file on Joe Bonds
Going Beyond Counting First Authors in Author Co-citation Analysis
Full text linkThe present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Nitrogen ligands: The transition metal catalyzed reaction of aryl halides with olefins (Mizoroki-Heck), phenylboronic acid (Suzuki coupling) and Buchwald-Hartwig amination, new catalysts and effect of co-catalysts<b> </b><b>—</b><b> </b>Aryl halide activation<b> </b><b>—</b><b> </b>Part I
No full text1894-1908Nitrogen ligands are an excellent alternative for the traditional
P-ligands in the Pd catalyzed Mizoroki-Heck reaction, Suzuki coupling and
Buchwald-Hartwig aryl amination. Pd complexes of dimethyl glyoxime,
8-hydroxyquinoline, salen, picolinic acid, and DAB ligands gave high yields of
the E-cinnamates and E-stilbenes from aryl iodides. Acetophenone
oxime N, N-dimethybenzylamine and ferrocenyl oxime palladacycle are better
catalysts with comparable yields, high TON (95, 000) and TOF's (2, 500 h-1) to P-ligand catalysts. Aryl bromides and
in a few cases, aryl chlorides could also be activated by these complexes by
the use of Lewis acid and (C4H9)4NI as
additives. Cy-DAB ligands gave good yields with electron rich aryl bromides and
the use of ionic liquid improve the yield. These N-ligand metal complexes can
be readily synthesized and the ligands possess the advantage of easy functional
group modifications and convenient synthetic methods compared to P-ligands. The
degradation reactions associated with P-ligands are not observed in the
N-ligands, with comparable, high thermal, moisture and air stability and
insensitivity. Activation of aryl bromides (Mizoroki-Heck reaction, Suzuki reaction)
could be achieved in high yields, TON and TOF (86-94% yield, TON: 36, 000-90,
000, TOF: 6, 000-11, 500 h-1) catalyzed by monomeric amine and oxime
palladacycles (Cat-8, 11, 13 B) with a N-heterocyclic carbene ligand
better than a phosphorous ligand. Molten (C4H9)4NBr
is an efficient ionic liquid medium for the Mizoroki-Heck reaction of aryl
bromides, giving higher yields. Low to moderate yields of aryl amination are
obtained with the carbene palladacycle and N, N-dibenzyl piperazine Pd
complexes
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