Conclusions. There is no basis for finding that the agreement discriminates against any telecommunications carrier not a party to the agreement.
Conclusions. Based upon the Internal Revenue Code of 1986, as amended (the "Code"), applicable Treasury Department regulations in effect as of the date hereof, current published administrative positions of the Internal Revenue Service contained in revenue rulings and procedures, and judicial decisions, and upon the assumptions and representations referred to herein and the documents provided to us by you (including the Proxy Statement and the Reorganization Agreement), it is our opinion for Federal income tax purposes that:
Conclusions. Stanxxx xxxcluded that, based upon and subject to its analysis, assumptions, limitations and qualifications cited in its opinion, and as of the date of the fairness opinion, the merger value to be paid in cash for the limited partner interests in connection with the mergers is fair from a financial point of view to the limited partner of each respective partnership. Compensation and Material Relationships. Stanxxx xxx been paid a fee of $200,000 in connection with the rendering of the fairness opinion. Such fee was not conditioned on Stanxxx'x xxxdings and is payable whether or not the mergers are consummated. In addition, Stanxxx xxxl be reimbursed for all reasonable out-of-pocket expenses, including legal fees, and will be indemnified against certain liabilities including certain liabilities under the securities laws. During the past two years, the partnerships had engaged Stanxxx xx render financial advisory services in connection with proposed transactions which were withdrawn and never consummated. In connection with such assignments Stanxxx xxx paid fees aggregating $125,000. ALTERNATIVE TRANSACTIONS TO THE MERGERS We considered the following alternative types of transactions before selecting the merger transaction described in this document. As discussed below, we believe that the mergers are the best available alternative for the partnerships to maximize the value of the partnerships' property interests.
Conclusions. There is no basis for finding that the amendment to the previously approved agreement discriminates against any telecommunications carrier not a party to the agreement.
Conclusions. Following the instructions above and providing accurate and readable text, tables, figures, and citations will help to make your report useful to readers. Scientists may read your report, as well as water planners, utility providers, and interested citizens. If your report successfully conveys accurate scientific information and explanations to these readers, we can help to create more informed decisions about the use, development, and management of water in the state.
Conclusions. If the College concludes that the charge of harassment is meritorious, it will provide timely notification to the accused of any corrective action proposed by the College.
Conclusions. The IN NRAs have consulted and closely cooperated and coordinated to reach agreement that they request an amendment to the IN cost sharing submitted by IN TSOs pursuant to Article 74 of CACM. The amended proposal should take into account the IN NRAs position stated above, and should be submitted by TSOs no later than 2 months after the last national decision to request an amendment has been made, in accordance with Article 9(12) of CACM.
Conclusions. In conclusion, we have developed a green version of organo- phosphorus-catalysed amide bond formation between unacti- vated aromatic carboxylic acids and amines. The commercially available pre-catalyst 3-methyl-1-phenyl-2-phospholene oxide 4 is reduced in situ by inexpensive and environmentally benign poly(methylhydrosiloxane) and bis( p-nitrophenyl) phosphate. With our newly developed method a wide variety of secondary and tertiary amides could be synthesised in very good to excel- lent yields. It is envisioned that organophosphorus catalysis will be a subject of extensive investigations in the upcoming years. Moreover, we believe that poly(methylhydrosiloxane) will find practical applications in several other common reactions in organic chemistry. Experimental A Radleys tube equipped with a magnetic stirbar was charged with carboxylic acid (0.5 mmol, 1.0 equiv.), phosphine oxide 4 (0.075 mmol or 0.125 mmol; 0.15 or 0.25 equiv.), and Published on 17 July 2017. Downloaded by Radboud University Nijmegen on 3/8/2019 8:23:31 AM. bis( p-nitrophenyl) phosphate (0.025 mmol, 0.05 equiv.). Subsequently toluene (2.5 mL, 0.2 M) was added, and to the formed suspension were added benzylamine (0.65 mmol, 1.3 equiv.), CCl4 (1.0 mmol, 2.0 equiv.), and poly(methyl- hydrosiloxane) (Mw 2450 Da, 0.12 mmol, 9 Si–H equiv.). The reaction was stirred at 110 °C for 20 hours. After cooling to room temperature, toluene was removed under reduced pressure and the crude product was resuspended in ethyl acetate (20 mL). The organic phase was washed with sat. aqueous NaHCO3 (2 × 20 mL), brine (1 × 20 mL), dried over Na2SO4, filtered, and evaporated. The crude product was puri- fied by silica column chromatography (ethyl acetate and n-heptane) to afford the desired amide. Conflict of interest There are no conflicts of interest to declare. Acknowledgements We thank Dr Xxxx Xxxxx for technical assistance with in situ VT 1H NMR and 31P NMR experiments. Notes and references 1 (a) X. X. xxx Xxxxxxxx, X. X. xxx Xxxxx and F. P. J. T. Rutjes, ChemSusChem, 2013, 6, 1615–1624; (b) X. Xxxxxxxxx and X. Xxxxx, Tetrahedron Lett., 2016, 57, 4443–4451. 2 (a) X. X. Xxxxxxx, X. X. XxXxxxxxx and X. XxXxxxxx-Xxxxx, Org. Lett., 2008, 10, 2589–2591; (b) X. Xxxx, X. Xxxxxxx, X. Xxxxxxx and X. Xxxxxx, Chem. Commun., 2014, 50, 7340–7343; (c) X. Xx, X. Xxxx, X. Xxxxx, X. Xxxxx and X. X. Xxxxxx, Tetrahedron, 2013, 69, 8769– 8776; (d) X. X. Xxxxxx, X. Xx, X. Xxxxxxxx, X. X. Xxxxx, X. Xxxxx and A. M. Xxxxxxx, X. Xxx....
Conclusions. In addition to the acetylenic transformations, leading to acetylene-based or benzenoid p-conjugated structures, the CuAAC reaction represents another powerful synthetic tool. Compared with other acetylenic reactions, a five-membered heteroaromatic ring is formed instead of an aromatic all-carbon ring. Employing its coordination and hydrogen- bond-accepting/-donating abilities, the triazole group brings new design opportunities; in addition to its heteroaromatic character, it can also serve as a functional building block. The conjugation- and function-related triazole-based materials, available to date, only started to appear few years ago; these examples, however, have highlighted the huge potential for new applications in different directions and opened a new sub-field within organic materials. We anticipate that this new class of materials may be applied in, for instance, sensors and responsive devices with well-defined tuneable (opto)electronic properties, and believe that this review will motivate future research in this field and add another brick on the road to carbon-rich functional materials. Acknowledgements Our thanks go to Xx Xxxxxx Xxxxxxxx, Xx´ n Xxxxx and Xx Xxxxx Xxxxxx Castriciano for their kind help, and to the Nederlandse Organisatie voor Wetenschappelijk Onderzoek (Netherlands Organisation for Scientific Research, NWO), NanoNed, Vici (A.E.R.), The Council for the Chemical Sciences of the Netherlands Organisation for Scientific Research and the European ITNs (CHEXTAN, SUPERIOR and HIERARCHY) for financial support. Notes and references 1 X. X. Xxxxx, X. X. Xxxxx, X. X. X’xxxxx, X. X. Xxxx and R. E. Xxxxxxx, Nature, 1985, 318, 162–163. 2 X. Xxxxxxxxx, Nature, 1994, 369, 199–207. 3 J.-X. Xx, X. Xxxxxx and X. Xx¨ llen, Chem. Rev., 2007, 107, 718–747.
Conclusions i. Concluding statement with reference to purpose of investigation and report
ii. Unanticipated conditions encountered
iii. Deviations from the plan (if any plan exists)
iv. Bedrock excavating conditions and rip ability
x. Xxxxx stability: Steepest cut slopes possible with a safety factor equal to or greater than 1:1 for a pseudo static condition.
vi. Surficial stability and erodibility of cut slopes and fill slopes
vii. Soil units
a. Classification