Bowen, M. E.; Monguchi, Y.; Sankaranarayanan, R.; Vagner, J.; Begay, L. J.; Xu, L.; Jagadish, B.; Hruby, V. J.; Gillies, R. J.; Mash, E. A. J. Org. Chem. 2007, 72, 1675 - 1680 and 3608.
Moore, W. R. A. D.; ODowd, M. In Properties and Applications of Polyvinyl Alcohol; Finch, C. A., Ed.; Staples Printers Ltd: Kent, England, 1968; Chapter 4, pp 77 - 87.
2; see: Sawyer, T. K.; Sanfilippo, P. J.; Hruby, V. J.; Engel, M. H.; Heward, C. B.; Burnett, J. B.; Hadley, M. E. Proc. Natl. Acad. Sci. U.S.A. 1980, 77, 5754-5758
2, was based on the minimal active sequence for full agonist activity of α-MSH; see
2, was based on the minimal active sequence for full agonist activity of α-MSH; see: Hruby, V. J.; Wilkes, B. C.; Hadley, M. E.; Al-Obeidi, F.; Sawyer, T. K.; Staples, D. J.; de Vaux, A. E.; Dym, O.; de L. Castrucci, A. M.; Hintz, M. F.; Riehm, J. P.; Rao, K. R. J. Med. Chem. 1987, 30, 2126-2130
Castrucci, A. M. L.; Hadley, M. E.; Sawyer, T. K.; Wilkes, B. C.; Al-Obiedi, F.; Staples, D. J.; de Vaux, A. E.; Dym, O.; Hintz, M. F.; Riehm, J. P.; Rao, K. R.; Hruby, V. J. Gen. Comp. Endocrinol. 1989, 73, 157-163
Xu, L.; Vagner, J.; Alleti, R.; Rao, V.; Jagadish, B.; Morse, D. L.; Hruby, V. J.; Gillies, R. J.; Mash, E. A. Bioorg. Med. Chem. Lett. 2010, 20, 2489-2492
This presumably was due to temporary intermolecular and intramolecular cross-linking during hydroboration, leading to sterically inaccessible, unreactive double bonds. Similar behavior was noted in previous work on the hydroboration of polyisoprene; see refs 8a-8d
This presumably was due to temporary intermolecular and intramolecular cross-linking during hydroboration, leading to sterically inaccessible, unreactive double bonds. Similar behavior was noted in previous work on the hydroboration of polyisoprene; see refs 8a-8d.
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Use of triisopinocampheyldiborane as described in ref 8b gave mixtures of polyols and isopinocampheol that were difficult to separate. The byproduct from use of disiamylborane, 3-methyl-2-butanol, was more easily removed from the polyol product under vacuum
Use of triisopinocampheyldiborane as described in ref 8b gave mixtures of polyols and isopinocampheol that were difficult to separate. The byproduct from use of disiamylborane, 3-methyl-2-butanol, was more easily removed from the polyol product under vacuum.
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0001319936
Sharma, S.; Oehlschlager, A. C. J. Org. Chem. 1989, 54, 5064-5073
Serine amide is commercially available from Senn Chemicals USA
Hidy, P. H.; Hodge, E. B.; Young, V. V.; Harned, R. L.; Brewer, G. A.; Phillips, W. F.; Runge, W. F.; Stavely, H. E.; Pohland, A.; Boaz, H.; Sullivan, H. R. J. Am. Chem. Soc. 1955, 77, 2345-2346 Serine amide is commercially available from Senn Chemicals USA.
Copper ion could not be removed by dialysis, presumably due to the strong chelatory properties of MSH(4)
Caplin, S. Tissue Cult. Assoc. Man. 1976, 2, 439-440 Copper ion could not be removed by dialysis, presumably due to the strong chelatory properties of MSH(4).
The hMC4R vector was originally received from Dr. Ira Gantz; see
The hMC4R vector was originally received from Dr. Ira Gantz; see: Gantz, I.; Miwa, H.; Konda, Y.; Shimoto, Y.; Tashiro, T.; Watson, S. J.; DelValle, J.; Yamada, T. J. Biol. Chem. 1993, 268, 15174-15179
The General Experimental section appears in the Supporting Information
The General Experimental section appears in the Supporting Information.
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This method was validated by titration of 0.10 M solutions of citronellal and geraniol in methanol with a 0.10 M solution of bromine in methanol. A negative control experiment with hexol A (see ref 2d for the preparation of A) gave a persistent bromine color upon addition of the first drop of bromine solution
This method was validated by titration of 0.10 M solutions of citronellal and geraniol in methanol with a 0.10 M solution of bromine in methanol. A negative control experiment with hexol A (see ref 2d for the preparation of A) gave a persistent bromine color upon addition of the first drop of bromine solution.
* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.