Статті в журналах з теми "N-N axially chiral molecules"
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Fukasawa, Sota, Tatsuya Toyoda, Ryohei Kasahara, Chisato Nakamura, Yuuki Kikuchi, Akiko Hori, Gary J. Richards, and Osamu Kitagawa. "Catalytic Enantioselective Synthesis of N-C Axially Chiral N-(2,6-Disubstituted-phenyl)sulfonamides through Chiral Pd-Catalyzed N-Allylation." Molecules 27, no. 22 (November 13, 2022): 7819. http://dx.doi.org/10.3390/molecules27227819.
Повний текст джерелаZhang, Xiaoke, Ya-Zhou Liu, Huawu Shao, and Xiaofeng Ma. "Advances in Atroposelectively De Novo Synthesis of Axially Chiral Heterobiaryl Scaffolds." Molecules 27, no. 23 (December 3, 2022): 8517. http://dx.doi.org/10.3390/molecules27238517.
Повний текст джерелаShi, Lei, Jiawei Zhu, Biqiong Hong, and Zhenhua Gu. "A Chiral Relay Race: Stereoselective Synthesis of Axially Chiral Biaryl Diketones through Ring-Opening of Optical Dihydrophenan-threne-9,10-diols." Molecules 28, no. 16 (August 8, 2023): 5956. http://dx.doi.org/10.3390/molecules28165956.
Повний текст джерелаCorti, Vasco, and Giulio Bertuzzi. "Organocatalytic Asymmetric Methodologies towards the Synthesis of Atropisomeric N-Heterocycles." Synthesis 52, no. 17 (June 15, 2020): 2450–68. http://dx.doi.org/10.1055/s-0040-1707814.
Повний текст джерелаPeerlings, H. W. I., and E. W. Meijer. "Synthesis and Characterization of Axially Chiral Molecules Containing Dendritic Substituents." European Journal of Organic Chemistry 1998, no. 4 (April 1998): 573–77. http://dx.doi.org/10.1002/(sici)1099-0690(199804)1998:4<573::aid-ejoc573>3.0.co;2-n.
Повний текст джерелаZeindlhofer, Veronika, Phillip Hudson, Ádám Márk Pálvölgyi, Matthias Welsch, Mazin Almarashi, H. Lee Woodcock, Bernard Brooks, Katharina Bica-Schröder, and Christian Schröder. "Enantiomerization of Axially Chiral Biphenyls: Polarizable MD Simulations in Water and Butylmethylether." International Journal of Molecular Sciences 21, no. 17 (August 28, 2020): 6222. http://dx.doi.org/10.3390/ijms21176222.
Повний текст джерелаWang, Jiaming, Changgui Zhao, and Jian Wang. "Recent Progress toward the Construction of Axially Chiral Molecules Catalyzed by an N-heterocyclic Carbene." ACS Catalysis 11, no. 20 (September 28, 2021): 12520–31. http://dx.doi.org/10.1021/acscatal.1c03459.
Повний текст джерелаSuzuki, Yuya, Masato Kageyama, Ryuichi Morisawa, Yasuo Dobashi, Hiroshi Hasegawa, Satoshi Yokojima, and Osamu Kitagawa. "The synthesis of optically active N–C axially chiral tetrahydroquinoline and its response to an acid-accelerated molecular rotor." Chemical Communications 51, no. 56 (2015): 11229–32. http://dx.doi.org/10.1039/c5cc03659c.
Повний текст джерелаMatsui, Ryosuke, Erina Niijima, Tomomi Imai, Hiroyuki Kobayashi, Akiko Hori, Azusa Sato, Yuko Nakamura, and Osamu Kitagawa. "Intermolecular Halogen Bond Detected in Racemic and Optically Pure N-C Axially Chiral 3-(2-Halophenyl)quinazoline-4-thione Derivatives." Molecules 27, no. 7 (April 6, 2022): 2369. http://dx.doi.org/10.3390/molecules27072369.
Повний текст джерелаKrishnamurthy, M. S., and Noor Shahina Begum. "Crystal structure of ethyl 2-cyano-3-[(1-ethoxyethylidene)amino]-5-(3-methoxyphenyl)-7-methyl-5H-1,3-thiazolo[3,2-a]pyrimidine-6-carboxylate." Acta Crystallographica Section E Crystallographic Communications 71, no. 4 (March 25, 2015): o256—o257. http://dx.doi.org/10.1107/s2056989015005241.
Повний текст джерелаTorii, Masahiro, Kohsuke Kato, Daisuke Uraguchi, and Takashi Ooi. "Chiral ammonium betaine-catalyzed asymmetric Mannich-type reaction of oxindoles." Beilstein Journal of Organic Chemistry 12 (September 28, 2016): 2099–103. http://dx.doi.org/10.3762/bjoc.12.199.
Повний текст джерелаTribedi, Soumi, and Raghavan B. Sunoj. "Molecular insights into chirality transfer from double axially chiral phosphoric acid in a synergistic enantioselective intramolecular amination." Chemical Science 13, no. 5 (2022): 1323–34. http://dx.doi.org/10.1039/d1sc05749a.
Повний текст джерелаZhang, Ming-Xing, Xin Chen, Kun-Lin Huang, Yi Zhu, and Shan-Shan Yang. "Distinct chiral units from an axially prochiral ligand in a photoluminescent zinc(II)–organic complex." Acta Crystallographica Section C Crystal Structure Communications 68, no. 4 (March 3, 2012): m90—m93. http://dx.doi.org/10.1107/s0108270112006051.
Повний текст джерелаNoor, Shabana, Shintaro Suda, Tomoyuki Haraguchi, Fehmeeda Khatoon, and Takashiro Akitsu. "Chiral crystallization of a zinc(II) complex." Acta Crystallographica Section E Crystallographic Communications 77, no. 5 (April 23, 2021): 542–46. http://dx.doi.org/10.1107/s2056989021003650.
Повний текст джерелаZhang, Ji-Wei, Shao-Hua Xiang, Shaoyu Li, and Bin Tan. "Copper-Catalyzed Synthesis of Axially Chiral Biaryls with Diaryliodonium Salts as Arylation Reagents." Molecules 26, no. 11 (May 27, 2021): 3223. http://dx.doi.org/10.3390/molecules26113223.
Повний текст джерелаDong, Ziyang, Chengming Jiang, and Changgui Zhao. "A Review on Generation and Reactivity of the N-Heterocyclic Carbene-Bound Alkynyl Acyl Azolium Intermediates." Molecules 27, no. 22 (November 17, 2022): 7990. http://dx.doi.org/10.3390/molecules27227990.
Повний текст джерелаYang, Xiaoqun, Tingting Li, Jinli Chen, Yixian Huang, Tingwei Shen, Shiguang Li, Zhichao Jin, and Shi-Chao Ren. "Carbene-Catalyzed Atroposelective Annulation for Quick Access to Axially Chiral Thiazine Derivatives." Molecules 28, no. 10 (May 12, 2023): 4052. http://dx.doi.org/10.3390/molecules28104052.
Повний текст джерелаHarada, Masashi, Sachise Karakawa, Hiroshi Miyano, and Kazutaka Shimbo. "Simultaneous Analysis of d,l-Amino Acids in Human Urine Using a Chirality-Switchable Biaryl Axial Tag and Liquid Chromatography Electrospray Ionization Tandem Mass Spectrometry." Symmetry 12, no. 6 (June 2, 2020): 913. http://dx.doi.org/10.3390/sym12060913.
Повний текст джерелаToze, Flavien A. A., Vladimir P. Zaytsev, Lala V. Chervyakova, Elisaveta A. Kvyatkovskaya, Pavel V. Dorovatovskii, and Victor N. Khrustalev. "Crystal structure of 3-benzyl-2-[(E)-2-(furan-2-yl)ethenyl]-2,3-dihydroquinazolin-4(1H)-one and 3-benzyl-2-[(E)-2-(thiophen-2-yl)ethenyl]-2,3-dihydroquinazolin-4(1H)-one from synchrotron X-ray diffraction." Acta Crystallographica Section E Crystallographic Communications 74, no. 1 (January 1, 2018): 10–14. http://dx.doi.org/10.1107/s2056989017017479.
Повний текст джерелаSato, Yasuhiro, Yuichi Kawata, Shungo Yasui, Yoshihito Kayaki, and Takao Ikariya. "New Bifunctional Bis(azairidacycle) with Axial Chirality via Double Cyclometalation of 2,2′-Bis(aminomethyl)-1,1′-binaphthyl." Molecules 26, no. 4 (February 22, 2021): 1165. http://dx.doi.org/10.3390/molecules26041165.
Повний текст джерелаSoloshonok, Vadim A., José Luis Aceña, Hisanori Ueki, and Jianlin Han. "Design and synthesis of quasi-diastereomeric molecules with unchanging central, regenerating axial and switchable helical chirality via cleavage and formation of Ni(II)–O and Ni(II)–N coordination bonds." Beilstein Journal of Organic Chemistry 8 (November 13, 2012): 1920–28. http://dx.doi.org/10.3762/bjoc.8.223.
Повний текст джерелаRoshchin, Alexander I., and Remir G. Kostyanovsky. "Configurationally stable axially chiral N,N’-dialkyl-2,2’-biphenylene-N,N’-ureas." Mendeleev Communications 13, no. 6 (January 2003): 275–76. http://dx.doi.org/10.1070/mc2003v013n06abeh001749.
Повний текст джерелаKikuchi, Yuki, Chisato Nakamura, Mizuki Matsuoka, Rina Asami, and Osamu Kitagawa. "Catalytic Enantioselective Synthesis of N–C Axially Chiral Sulfonamides through Chiral Palladium-Catalyzed N-Allylation." Journal of Organic Chemistry 84, no. 12 (May 22, 2019): 8112–20. http://dx.doi.org/10.1021/acs.joc.9b00989.
Повний текст джерелаBrunner, H., G. Olschewski, and B. Nuber. "Enantioselective Catalyses; 126: Axially Chiral N,N-Ligands with Binaphthyl/Bipyridyl Structure." Synthesis 1999, no. 03 (March 1999): 429–34. http://dx.doi.org/10.1055/s-1999-3424.
Повний текст джерелаKawabata, Takeo, Changsheng Jiang, Kazuhiro Hayashi, Kazunori Tsubaki, Tomoyuki Yoshimura, Swapan Majumdar, Takahiro Sasamori, and Norihiro Tokitoh. "Axially Chiral Binaphthyl Surrogates with an Inner N−H−N Hydrogen Bond." Journal of the American Chemical Society 131, no. 1 (January 14, 2009): 54–55. http://dx.doi.org/10.1021/ja808213r.
Повний текст джерелаVekemans, Jozef A. J. M., Jeroen A. F. Boogers, and Henk M. Buck. "Conformational interlocking in axially chiral methyl N-(2',4'-dimethylnicotinoyl)-N-methylphenylalaninates." Journal of Organic Chemistry 56, no. 1 (January 1991): 10–16. http://dx.doi.org/10.1021/jo00001a005.
Повний текст джерелаKoide, Hiroshige, Motokazu Uemura, and Motokazu Uemura. "Synthesis of axially chiral N,N-diethyl 2,6-disubstituted benzamides utilizing planar chiral (arene)chromium complexes." Chemical Communications, no. 22 (1998): 2483–84. http://dx.doi.org/10.1039/a806064i.
Повний текст джерелаKotora, Martin. "Synthesis of axially chiral bipyridine N,N'-dioxides and enantioselective allylation of aldehydes." Pure and Applied Chemistry 82, no. 9 (June 7, 2010): 1813–26. http://dx.doi.org/10.1351/pac-con-09-10-01.
Повний текст джерелаPan, Ming, Ying-Bo Shao, Qun Zhao, and Xin Li. "Asymmetric Synthesis of N–N Axially Chiral Compounds by Phase-Transfer-Catalyzed Alkylations." Organic Letters 24, no. 1 (December 20, 2021): 374–78. http://dx.doi.org/10.1021/acs.orglett.1c04028.
Повний текст джерелаFrey, Johanna, Sabine Choppin, Françoise Colobert, and Joanna Wencel-Delord. "Towards Atropoenantiopure N–C Axially Chiral Compounds via Stereoselective C–N Bond Formation." CHIMIA International Journal for Chemistry 74, no. 11 (November 25, 2020): 883–89. http://dx.doi.org/10.2533/chimia.2020.883.
Повний текст джерелаWu, Shijie, Yongfei Xing, Jie Wang, Xingchen Guo, Huajie Zhu, and Wan Li. "Axially chiral N,N′‐ dioxides ethers for catalysis in enantioselective allylation of aldehydes." Chirality 31, no. 11 (August 28, 2019): 947–57. http://dx.doi.org/10.1002/chir.23122.
Повний текст джерелаYe, Chen‐Xi, Shuming Chen, Feng Han, Xiulan Xie, Sergei Ivlev, K. N. Houk, and Eric Meggers. "Atroposelective Synthesis of Axially Chiral N‐Arylpyrroles by Chiral‐at‐Rhodium Catalysis." Angewandte Chemie 132, no. 32 (June 3, 2020): 13654–58. http://dx.doi.org/10.1002/ange.202004799.
Повний текст джерелаYe, Chen‐Xi, Shuming Chen, Feng Han, Xiulan Xie, Sergei Ivlev, K. N. Houk, and Eric Meggers. "Atroposelective Synthesis of Axially Chiral N‐Arylpyrroles by Chiral‐at‐Rhodium Catalysis." Angewandte Chemie International Edition 59, no. 32 (June 3, 2020): 13552–56. http://dx.doi.org/10.1002/anie.202004799.
Повний текст джерелаNakazaki, Atsuo, Keitaro Miyagawa, Noriaki Miyata, and Toshio Nishikawa. "ChemInform Abstract: Synthesis of a C-N Axially Chiral N-Arylisatin Through Asymmetric Intramolecular N-Arylation." ChemInform 46, no. 48 (November 12, 2015): no. http://dx.doi.org/10.1002/chin.201548124.
Повний текст джерелаGarcía-González, Ángel, Leland Belda, Alejandro Manchado, Carlos T. Nieto, and Narciso Martín Garrido. "(R)-N-Benzyl-N-(1-phenylethyl)cyclohexanamine." Molbank 2023, no. 1 (January 20, 2023): M1561. http://dx.doi.org/10.3390/m1561.
Повний текст джерелаChen, Jin-fang, Jin-yi Shi, Cong-cong Yin, Xin Cui, Guang-xun Li, Zhuo Tang, and Jin-zhong Zhao. "Synthesis of axially chiral N-aryl benzimidazoles via chiral phosphoric acid catalyzed enantioselective oxidative aromatization." New Journal of Chemistry 46, no. 14 (2022): 6398–402. http://dx.doi.org/10.1039/d1nj06092a.
Повний текст джерелаKinoshita, Shunsuke, and Ken Kamikawa. "Stereoselective synthesis of N-arylindoles and related compounds with axially chiral N–C bonds." Tetrahedron 72, no. 34 (August 2016): 5202–7. http://dx.doi.org/10.1016/j.tet.2015.11.053.
Повний текст джерелаFUJII, M., and A. HONDA. "ChemInform Abstract: Preparation of an Axially Chiral Heteroaromatic Compound 1,1′- Biisoquinoline-N,N′-dioxide." ChemInform 23, no. 31 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199231195.
Повний текст джерелаKamikawa, K., M. Uemura, S. Kinoshita, and H. Matsuzaka. "Formation of Axially Chiral N-Aryl Indoles and Stereoselective Functionalization." Synfacts 2006, no. 5 (May 2006): 0466. http://dx.doi.org/10.1055/s-2006-934353.
Повний текст джерелаShimizu, Ken D., Heather O. Freyer, and Richard D. Adams. "Synthesis, resolution and structure of axially chiral atropisomeric N-arylimides." Tetrahedron Letters 41, no. 29 (July 2000): 5431–34. http://dx.doi.org/10.1016/s0040-4039(00)00835-2.
Повний текст джерелаRokade, Balaji V., and Patrick J. Guiry. "Axially Chiral P,N-Ligands: Some Recent Twists and Turns." ACS Catalysis 8, no. 1 (December 26, 2017): 624–43. http://dx.doi.org/10.1021/acscatal.7b03759.
Повний текст джерелаLin, Wei, Qun Zhao, Yao Li, Ming Pan, Chen Yang, Guo-Hui Yang, and Xin Li. "Asymmetric synthesis of N–N axially chiral compounds via organocatalytic atroposelective N-acylation." Chemical Science 13, no. 1 (2022): 141–48. http://dx.doi.org/10.1039/d1sc05360d.
Повний текст джерелаKoide, Hiroshige, and Motokazu Uemura. "Axially chiral benzamides: Diastereoselective nucleophilic additions to planar chiral (N, N-diethyl-2-acyl-6-methylbenzamide)chromium complexes." Tetrahedron Letters 40, no. 17 (April 1999): 3443–46. http://dx.doi.org/10.1016/s0040-4039(99)00462-1.
Повний текст джерелаZhou, Qian-Yi, and Xin Li. "Atroposelective construction of axially chiral enamides via N-allylic alkylation." Chemical Communications 58, no. 30 (2022): 4727–30. http://dx.doi.org/10.1039/d2cc01000c.
Повний текст джерелаRen, Qiao, Tingting Cao, Chunnian He, Meihua Yang, Haitao Liu, and Lei Wang. "Highly Atroposelective Rhodium(II)-Catalyzed N–H Bond Insertion: Access to Axially Chiral N-Arylindolocarbazoles." ACS Catalysis 11, no. 10 (May 6, 2021): 6135–40. http://dx.doi.org/10.1021/acscatal.1c01232.
Повний текст джерелаBrunner, H., G. Olschewski, and B. Nuber. "ChemInform Abstract: Enantioselective Catalyses. Part 126. Axially Chiral N,N-Ligands with Binaphthyl/Bipyridyl Structure." ChemInform 30, no. 27 (June 15, 2010): no. http://dx.doi.org/10.1002/chin.199927158.
Повний текст джерелаKotora, Martin. "ChemInform Abstract: Synthesis of Axially Chiral Bipyridine N,N′-Dioxides and Enantioselective Allylation of Aldehydes." ChemInform 42, no. 9 (February 3, 2011): no. http://dx.doi.org/10.1002/chin.201109268.
Повний текст джерелаYang, Guo-Hui, Hanliang Zheng, Xin Li, and Jin-Pei Cheng. "Asymmetric Synthesis of Axially Chiral Phosphamides via Atroposelective N-Allylic Alkylation." ACS Catalysis 10, no. 3 (January 17, 2020): 2324–33. http://dx.doi.org/10.1021/acscatal.9b05443.
Повний текст джерелаBrown, Richard J., Gary Annis, Albert Casalnuovo, Dominic Chan, Rafael Shapiro, and William J. Marshall. "Synthesis and properties of axially-chiral N-(2,6-disubstituted)phenyl triazolones." Tetrahedron 60, no. 20 (May 2004): 4361–75. http://dx.doi.org/10.1016/j.tet.2004.03.056.
Повний текст джерелаLi, Dawei, Sijing Wang, Shulin Ge, Shunxi Dong, and Xiaoming Feng. "Asymmetric Synthesis of Axially Chiral Anilides via Organocatalytic Atroposelective N-Acylation." Organic Letters 22, no. 14 (June 30, 2020): 5331–36. http://dx.doi.org/10.1021/acs.orglett.0c01581.
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