Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Damon Parrish"'
Autor:
Mao-Xi Zhang, Nathaniel B. Zuckerman, Philip F. Pagoria, Bradley A. Steele, I-Feng Kuo, Gregory H. Imler, Damon Parrish
Publikováno v:
Molecules, Vol 26, Iss 14, p 4209 (2021)
Mono- and dinitro-BN-naphthalenes, i.e., 1-nitro-, 3-nitro-, 1,6-dinitro-, 3,6-dinitro-, and 1,8-dinitro-BNN, were generated in the nitration of 9,10-BN-naphthalene (BNN), a boron–nitrogen (BN) bond-embedded naphthalene, with AcONO2 and NO2BF4 in a
Externí odkaz:
https://doaj.org/article/d02e7ab88b444d848a8afcb5847fcbdf
Autor:
Damon Parrish, Andrew Purdy
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 3, Pp m147-m147 (2013)
The title compound, [Al2K2(C2H6N)8(C4H8O)]n, formed during the sonochemical reaction between Al(NMe2)3 and sodium–potassium alloy in the presence of tetrahydrofuran (THF). Its asymmetric unit has two inequivalent K+ sites. One site is coordinated b
Externí odkaz:
https://doaj.org/article/b9634d94eba94f8682a3c3311d0191dc
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 10, Pp o2355-o2355 (2009)
The title compound, C4H2BrNO3, is one of a series of three substituted oxauracils prepared as precursors in the preparation of 1-aza-1,3-butadienes. Although each structure has identical potential for N—H...O intermolecular hydrogen bonds, each for
Externí odkaz:
https://doaj.org/article/5447994118cb4d0f9d00e8e29d8b496a
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 10, Pp o2354-o2354 (2009)
In the title compound, C5H5NO3, the planar (maximum deviation = 0.075 Å for the ring O atom) molecules form N—H...O hydrogen bonds in a zigzag chain (C—O...N bond angle ≃ 140°) between glide-related molecules.
Externí odkaz:
https://doaj.org/article/34620e37a46c4464b0c55d2798380bd8
Publikováno v:
Acta Crystallographica Section E, Vol 65, Iss 10, Pp o2356-o2356 (2009)
In the title compound, C4HCl2NO3, the essentially planar (maximum deviation = 0.023 Å for the ring O atom) molecules form N—H...O hydrogen bonds between molecules lying about inversion centers, forming eight-membered rings with an R22(8) motif in
Externí odkaz:
https://doaj.org/article/afbd6c59701340029aa9019a96099a91
Publikováno v:
Journal of the American Chemical Society. 131:12240-12249
In order to understand how electronic and other structural characteristics of biphenyl phosphine ligands affect Pd-catalyzed C-N and C-C bond-forming reactions, a new ligand, 2-(dicyclohexylphosphino)-4'-(N,N-dimethylamino)-1,1'-biphenyl, was synthes
Autor:
Jeewoo Lee, Thushara P. Abeyweera, Damon Parrish, Alyson R. Baker, Robert J. Surawski, Matthew R. Young, Jean-Philip Truman, Nancy H. Colburn, Adriana Haimovitz-Friedman, Hee Kim, Young Ho Kim, Victor E. Marquez, Dehui Duan, Peter M. Blumberg, Nicholas A. Perry, Howard A. Young, Nancy E. Lewin, Jeffrey R. Deschamps, Noemi Kedei, Jae-Uk Chung, Megan L. Peach, James A. Kelley, Saïd El Kazzouli, Christopher C. Lai, Dina M. Sigano, Susan A. Rotenberg
Publikováno v:
Journal of Medicinal Chemistry. 51:5198-5220
Diacylglycerol-lactone (DAG-lactone) libraries generated by a solid-phase approach using IRORI technology produced a variety of unique biological activities. Subtle differences in chemical diversity in two areas of the molecule, the combination of wh
Autor:
Raja Duddu, Paritosh R. Dave, Reddy Damavarapu, Rao Surapaneni, Richard Gilardi, Damon Parrish
Publikováno v:
Synthetic Communications. 38:767-774
Syntheses of azido derivatives of hexaazaisowurtzitane, triazine, and tetrazine heterocyclic compounds are described.
Autor:
Anthony Lozama, John S. Partilla, Thomas E. Prisinzano, Denise S. Simpson, Damon Parrish, Hernán A. Navarro, Peter L. Katavic, Christina M. Dersch, Wayne W. Harding, Jeffrey R. Deschamps, Richard B. Rothman
Publikováno v:
Journal of Medicinal Chemistry. 50:3596-3603
Further modification of salvinorin A (1a), the major active component of Salvia divinorum, has resulted in the synthesis of novel neoclerodane diterpenes with opioid receptor affinity and activity. We report in this study that oxadiazole 11a and salv
Autor:
Carmen I. Mitan, Damon Parrish, and Kenneth R. Phares, ‡ Norica Branzǎ-Nichita, Robert M. Moriarty
Publikováno v:
Organic Letters. 8:3465-3467
A facile synthesis is reported for five-membered iminocyclitols which allows for variation in stereochemistry at all the chiral centers, diverse C1- and N-substitution, and the potential for a three-component combinatorial process. The key step is in