Log in

Relevant bibliographies by topics / 6-azabicyclo[3.2.0]heptane / Journal articles

To see the other types of publications on this topic, follow the link: 6-azabicyclo[3.2.0]heptane.

Journal articles on the topic '6-azabicyclo[3.2.0]heptane'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic '6-azabicyclo[3.2.0]heptane.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Butcher, Ray J., Yousef M. Hijji, and Ellis Benjamin. "cis-3-Azabicyclo[3.2.0]heptane-2,4-dione." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (March 8, 2006): o1266—o1268. http://dx.doi.org/10.1107/s1600536806006933.

Full text

Abstract:

The title compound, C6H7NO2, was synthesized from cis-1,2-cyclobutanedicarboxylic anhydride by reaction with ammonium acetate under microwave conditions. The crystal structure of the compound shows that the cyclobutane ring is planar with angles ranging from 89.64 (12) to 90.37 (12)°. The cis-3-azabicyclo[3.2.0]heptane-2,4-dione molecules are linked into a chain formation through hydrogen N—H...O=C bonds. Parallel packing is seen between two cyclobutane rings related by inversion symmetry.

APA, Harvard, Vancouver, ISO, and other styles

2

Usman, Anwar, Ibrahim Abdul Razak, Hoong-Kun Fun, Suchada Chantrapromma, Bao-Guo Zhao, and Jian-Hua Xu. "1,5-Dichloro-3,6,6-triphenyl-3-azabicyclo[3.2.0]heptane-2,4-dione." Acta Crystallographica Section E Structure Reports Online 57, no. 8 (July 27, 2001): o792—o793. http://dx.doi.org/10.1107/s1600536801012673.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Hijji, Yousef M., Ellis Benjamin, Earl Benjamin, Ray J. Butcher, and Jerry P. Jasinski. "3-(2,6-Dioxopiperidin-3-yl)-3-azabicyclo[3.2.0]heptane-2,4-dione." Acta Crystallographica Section E Structure Reports Online 65, no. 2 (January 28, 2009): o394—o395. http://dx.doi.org/10.1107/s1600536809002839.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Saouane, Sofiane, Gernot Buth, and Francesca P. A. Fabbiani. "Crystal structure and packing energy calculations of (+)-6-aminopenicillanic acid." Acta Crystallographica Section C Crystal Structure Communications 69, no. 11 (October 24, 2013): 1238–42. http://dx.doi.org/10.1107/s0108270113025924.

Full text

Abstract:

The X-ray single-crystal structure of (2S,5R,6R)-6-amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, commonly known as (+)-6-aminopenicillanic acid (C8H12N2O3S) and a precursor of a variety of semi-synthetic penicillins, has been determined from synchrotron data at 150 K. The structure represents an ordered zwitterion and the crystals are nonmerohedrally twinned. The crystal structure is composed of a three-dimensional network built by three charge-assisted hydrogen bonds between the ammonium and carboxylate groups. The complementary analysis of the crystal packing by thePIXELmethod brings to light the nature and ranking of the energetically most stabilizing intermolecular interaction energies. In accordance with the zwitterionic nature of the structure,PIXELlattice energy calculations confirm the predominance of the Coulombic term (−379.1 kJ mol−1) ahead of the polarization (−141.4 kJ mol−1), dispersion (−133.7 kJ mol−1) and repulsion (266.3 kJ mol−1) contributions.

APA, Harvard, Vancouver, ISO, and other styles

5

Reck, G., J. Ječný, K. Huml, and J. Symerský. "Structure of 6-azabicyclo[3.2.0]heptan-7-one." Acta Crystallographica Section C Crystal Structure Communications 46, no. 4 (April 15, 1990): 720–22. http://dx.doi.org/10.1107/s0108270189011832.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Ji, Jianguo, William H. Bunnelle, Tao Li, Jennifer M. Pace, Michael R. Schrimpf, Kevin B. Sippy, David J. Anderson, and Michael D. Meyer. "Discovery of fused azetidines as novel selective α4β2 neuronal nicotinic receptor (NNR) agonists." Pure and Applied Chemistry 77, no. 12 (January 1, 2005): 2041–45. http://dx.doi.org/10.1351/pac200577122041.

Full text

Abstract:

An efficient synthesis of (1R,5S)-6-(5-cyano-3-pyridinyl)-3,6-diaza-bicyclo[3.2.0]heptane A-366833, a novel potent selective neuronal nicotinic receptor (NNR) agonist, is described. The enantiomerically pure pharmacophore benzyl (1S,5S)-3,6-diaza-bicyclo[3.2.0]heptane-3-carbamate was successfully constructed from benzyl N-allyl-N-(2-hydroxyimino-ethyl)-carbamate through a convenient approach including an intramolecular [1,3]-dipolar cycloaddition, reductive ring-opening reaction, chiral resolution, and intramolecular cyclization. Subsequent N-arylation of the pharmacophore with 3-bromo-5-cyanopyridine and N-Cbz deprotection with trifluoroacetic acid furnished A-366833.

APA, Harvard, Vancouver, ISO, and other styles

7

Homon, Anton A., Oleksandr V. Hryshchuk, Serhii Trofymchuk, Oleg Michurin, Yuliya Kuchkovska, Dmytro S. Radchenko, and Oleksandr O. Grygorenko. "Synthesis of 3-Azabicyclo[3.2.0]heptane-Derived Building Blocks via [3+2] Cycloaddition." European Journal of Organic Chemistry 2018, no. 40 (October 1, 2018): 5596–604. http://dx.doi.org/10.1002/ejoc.201800972.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Reinart-Okugbeni, Reet, Kerti Ausmees, Kadri Kriis, Franz Werner, Ago Rinken, and Tõnis Kanger. "Chemoenzymatic synthesis and evaluation of 3-azabicyclo[3.2.0]heptane derivatives as dopaminergic ligands." European Journal of Medicinal Chemistry 55 (September 2012): 255–61. http://dx.doi.org/10.1016/j.ejmech.2012.07.025.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Glass, Timothy E., and Phyllis A. Leber. "The thermal rearrangement of 6-methyl-6-vinylbicyclo)[3.2.0]heptane." Tetrahedron Letters 31, no. 8 (January 1990): 1085–88. http://dx.doi.org/10.1016/s0040-4039(00)88732-8.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Steiner, Gerd, Rainer Munschauer, Gerhard Klebe, and Lorenz Siggel. "Diastereoselective Synthesis of Exo-6-aryl-3-azabicyclo[3.2.0]heptane Derivatives by Intramolecular [2+2]Photocycloadditions of Diallylic Amines." HETEROCYCLES 40, no. 1 (1995): 319. http://dx.doi.org/10.3987/com-94-s34.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Reinart-Okugbeni, Reet, Kerti Ausmees, Kadri Kriis, Franz Werner, Ago Rinken, and Tonis Kanger. "ChemInform Abstract: Chemoenzymatic Synthesis and Evaluation of 3-Azabicyclo[3.2.0]heptane Derivatives as Dopaminergic Ligands." ChemInform 44, no. 3 (January 15, 2013): no. http://dx.doi.org/10.1002/chin.201303103.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Honda, Kiyoshi, Mari Konishi, Manabu Kawai, Akihisa Yamada, Yasuhiko Takahashi, Yujiro Hoshino, and Seiichi Inoue. "Stereoselective Synthesis of Bicyclo[3.1.1]Heptane Derivatives via Intramolecular Photocycloaddition Reaction." Natural Product Communications 7, no. 4 (April 2012): 1934578X1200700. http://dx.doi.org/10.1177/1934578x1200700410.

Full text

Abstract:

Optically active 1,3-bridged cyclobutanes 10 of the bicyclo[3.1.1]heptane ring system and 1,2-bridged cyclobutanes 11 of the bicyclo[3.2.0]heptane ring system were produced by UV irradiation of α,β,γ,δ-unsaturated esters 9a and 9c-f. The preference of endo-stereochemistry at C-6 bridged head was observed in cross-adducts 10. On the other hand, irradiation of conjugated dienol9b led via only parallel cycloaddition to 1,2-bridged cyclobutane 11.

APA, Harvard, Vancouver, ISO, and other styles

13

Otuokere, Ifeanyi Edozie, and Unwanaobong Friday Robert. "Synthesis, Characterization and Antibacterial Studies of (3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid-Cr (III) Complex." Journal of Nepal Chemical Society 41, no. 1 (July 29, 2020): 1–7. http://dx.doi.org/10.3126/jncs.v41i1.30370.

Full text

Abstract:

Benzylpenicillin, also known as (3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic, is a common bactericidal antibiotic of the betalactamin family which is mostly used to treat infections caused by gram-positive bacterial strains and few gram-negative bacterial strains. Cr (III) complex of benzylpenicillin was synthesized by the reaction of benzylpenicillin with CrCl3.6H2O. The structure of the complex was confirmed through elemental analysis, electrical conductivity, FT-IR, electronic spectra, 1H-NMR, and 13C-NMR spectroscopic methods. The physical properties such as solubility, color and melting point were also determined for both the ligand and the complex. The complex has a deep green color. Both the ligand and the complex are ionic (236.0 and 126.0 Sm2.mol-1). From the spectroscopic result, the ligand behaved as a pentadentate ligand coordinating to the metal ion through OH, NH, C=O of amide, carboxylate& β-lactam. A trigonal bipyramidal geometry has been proposed for the metal complex. The prepared complex was evaluated in vitro for its antibacterial activity against some pathogenic gram-positive (Staphylococcus aureus, Bacillus substilis, Bacillus cereus, and Enterococcus faecalis) and gram-negative bacteria (Escherichia coli, Enterobacter cloacae, Pneumonia aeruginosa and Campylobacter fetus). The metal complex showed enhanced antibacterial activity as compared to the uncomplexed ligand.

APA, Harvard, Vancouver, ISO, and other styles

14

STEINER, G., R. MUNSCHAUER, G. KLEBE, and L. SIGGEL. "ChemInform Abstract: Diastereoselective Synthesis of exo-6-Aryl-3-azabicyclo(3.2.0)heptane Derivatives by Intramolecular (2 + 2) Photocycloadditions of Diallylic Amines." ChemInform 26, no. 28 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199528120.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Chiba, Takuo, Takumi Takahashi, Junichi Sakaki, and Chikara Kaneko. "A simple method for synthesizing 7-oxo-4-thia-1-azabicyclo(3.2.0)heptane and its 6-methyl derivatives from ethyl cyanoacetate." CHEMICAL & PHARMACEUTICAL BULLETIN 33, no. 7 (1985): 3046–49. http://dx.doi.org/10.1248/cpb.33.3046.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Demchuk, Oleksandr P., Oleksandr V. Hryshchuk, Bohdan V. Vashchenko, Andriy V. Kozytskiy, Andriy V. Tymtsunik, Igor V. Komarov, and Oleksandr O. Grygorenko. "Photochemical [2 + 2] Cycloaddition of Alkenyl Boronic Derivatives: An Entry into 3-Azabicyclo[3.2.0]heptane Scaffold." Journal of Organic Chemistry 85, no. 9 (April 1, 2020): 5927–40. http://dx.doi.org/10.1021/acs.joc.0c00265.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

FRANZISKET, L., and A. HEESING. "ChemInform Abstract: Regio- and Stereoselectivity in Anionic Ring Opening Reactions of 2- Azabicyclo(3.2.0)heptane Derivatives." ChemInform 22, no. 22 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199122064.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Sano, Takehiro, Kazuhiko Tanaka, Yoshie Horiguchi, and Yoshisuke Tsuda. "Azabiocyclo[3.2.0]heptane-3,4-dione (10): A Thermal Azonia 1,3-Shift of 2-Azabicyclo[3.2.0]hept-2-enes to 2-Azanorborn-2-enes." HETEROCYCLES 23, no. 4 (1985): 813. http://dx.doi.org/10.3987/r-1985-04-0813.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Petz, Susanne, and Klaus T. Wanner. "Synthesis of 3-Azabicyclo[3.2.0]heptane Derivatives as γ-Aminobutyric Acid Analogues through Intermolecular [2+2] Photocycloaddition." European Journal of Organic Chemistry 2013, no. 19 (May 14, 2013): 4017–25. http://dx.doi.org/10.1002/ejoc.201201723.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Usman, Anwar, Ibrahim Abdul Razak, Hoong-Kun Fun, Suchada Chantrapromma, Bao-Guo Zhao, and Jian-Hua Xu. "1,5-Dichloro-3,6-diphenyl-3-azabicyclo[3.2.0]hept-6-ene-2,4-dione." Acta Crystallographica Section E Structure Reports Online 57, no. 10 (September 29, 2001): o990—o991. http://dx.doi.org/10.1107/s1600536801015665.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Longobardi, Lauren E., Tayseer Mahdi, and Douglas W. Stephan. "B(C6F5)3 mediated arene hydrogenation/transannulation of para-methoxyanilines." Dalton Transactions 44, no. 16 (2015): 7114–17. http://dx.doi.org/10.1039/c5dt00921a.

Full text

Abstract:

The stoichiometric reaction of para-methoxyanilines and B(C₆F₅)₃ under H₂ results in reduction of the N-bound phenyl ring(s), and subsequent transannular ring closure with elimination of methanol, affording the respective 7-azabicyclo[2.2.1]heptane derivatives.

APA, Harvard, Vancouver, ISO, and other styles

22

Walker, Daniel, Donn Wishka, Paul Beagley, Jessica Lyon, and Kathleen Farley. "A Concise Synthesis of 6-Oxa-3-azabicyclo[3.1.1]heptane Hydrotosylate." Synthesis 2011, no. 16 (July 14, 2011): 2619–24. http://dx.doi.org/10.1055/s-0030-1260116.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Donati, Daniele, Carla Marchioro, Bruno Tamburini, and Antonella Ursini. "STEREOSELECTIVE REDUCTION OF PIVALOYLOXYMETHYL (2S,5R,6S)-6-ACETYL-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLATE WITH SODIUM BOROHYDRIDE." Organic Preparations and Procedures International 24, no. 1 (February 1992): 48–51. http://dx.doi.org/10.1080/00304949209356696.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Poveda, J. C., J. A. Henao, J. A. Pinilla, V. V. Kouznetsov, and C. Ochoa. "X-ray powder diffraction analysis of 2-exo-(β-pyridyl)-6-exo-phenyl-7-oxa-1-azabicyclo[2.2.1]heptane." Powder Diffraction 18, no. 1 (March 2003): 47–49. http://dx.doi.org/10.1154/1.1515298.

Full text

Abstract:

The X-ray powder diffraction pattern for a bridgehead heterocyclic system was determined. 2-exo-(β-pyridyl)-6-exo-phenyl-7-oxa-1-azabicyclo[2.2.1]heptane, C16H16N2O, is triclinic with refined unit cell parameters a=1.1012(2), b=1.3950(2), c=1.0074(3) nm, α=111.09(2)°, β=104.97(2)°, γ=77.38(2)°, V=1.3813(3) nm3, Z=4, and Dx=1.212 g/cm3 with space group P-1 (No. 2).

APA, Harvard, Vancouver, ISO, and other styles

25

Barrett, Anthony G. M., Minn-Chang Cheng, Santi Sakdarat, Christopher D. Spilling, and Sven J. Taylor. "Stereocontrolled total synthesis of the penicillanate ester (2S,5R)-benzyl 3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0] heptane-2-carboxylate." Tetrahedron Letters 30, no. 18 (1989): 2349–50. http://dx.doi.org/10.1016/s0040-4039(01)80395-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Tang, Chao, Li Cai, Shuai Liu, Zhiwei Zheng, Gen Li, Jianli Chen, and Qiang Sui. "Crystal structure of tebipenem pivoxil." Acta Crystallographica Section E Crystallographic Communications 74, no. 9 (August 10, 2018): 1215–17. http://dx.doi.org/10.1107/s2056989018010770.

Full text

Abstract:

The molecular structure of the first orally active carbapenem antibacterial agent, tebipenem pivoxil (systematic name: (2,2-dimethylpropanoyloxy)methyl (4R,5S,6S)-3-{[1-(4,5-dihydro-1,3-thiazol-2-yl)azetidin-3-yl]sulfanyl}-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate), C22H31N3O6S2, has been determined and the configurations of the four chiral centers validated. The title compound crystallizes in the triclinic space group P1 with one molecule in the unit cell. Three out of the four rings adopt planar conformations while the thiazolinyl ring adopts an enveloped conformation. In the crystal, O—H...N hydrogen bonds link the molecules into chains along [1\overline{1}0].

APA, Harvard, Vancouver, ISO, and other styles

27

Chiba, Takuo, Jun-ichi Sakaki, Takumi Takahashi, and Chikara Kaneko. "A SHORT SYNTHESIS OF 7-OXO-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE. A BASIC SKELETON OF PENICILLIN-TYPE β-LACTAMS." Chemistry Letters 14, no. 5 (May 5, 1985): 659–60. http://dx.doi.org/10.1246/cl.1985.659.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

SANO, Takehiro, Yoshie HORIGUCHI, Kazuhiko TANAKA, Ken-ichi ABE, and Yoshisuke TSUDA. "Dioxopyrrolines. XLII. Mechanism of 7-epimerization reaction of 7-substituted 5-ethoxycarbonyl-1-phenyl-2-azabicyclo[3.2.0]heptane-3,4-diones." CHEMICAL & PHARMACEUTICAL BULLETIN 37, no. 3 (1989): 652–59. http://dx.doi.org/10.1248/cpb.37.652.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Bateson, John H., Stephen C. M. Fell, Robert Southgate, and John W. Tyler. "Olivanic acid analogues. Part 7. Lead tetra-acetate oxidation of 3-alkylthio-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylates." Journal of the Chemical Society, Perkin Transactions 1, no. 9 (1990): 2553. http://dx.doi.org/10.1039/p19900002553.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

DONATI, D., C. MARCHIORO, B. TAMBURINI, and A. URSINI. "ChemInform Abstract: Stereoselective Reduction of Pivaloyloxymethyl (2S,5R,6S)-6-Acetyl-3,3- dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylate with Sodium Borohydride." ChemInform 23, no. 36 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199236275.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

SANO, Takehiro, Yoshie HORIGUCHI, Suetaka KAMBE, Kazuhiko TANAKA, Jun'ichi TAGA, Jun TODA, and Yoshisuke TSUDA. "Dioxopyrrolines. XLVII. Thermal rearrangements of 7-vinyl derivatives of 1-aryl-5-ethoxycarbonyl-2-azabicyclo(3.2.0)heptane-3,4-diones and their imidates." CHEMICAL & PHARMACEUTICAL BULLETIN 38, no. 5 (1990): 1170–75. http://dx.doi.org/10.1248/cpb.38.1170.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Pombo-Villar, E., P. Supavilai, H. P. Weber, and H. W. G. M. Boddeke. "6-Carboxymethyl-2-azabicyclo[2.2.1]heptane enantiomers: muscarinic activities of rigid analogues of arecoline." Bioorganic & Medicinal Chemistry Letters 2, no. 5 (January 1992): 501–4. http://dx.doi.org/10.1016/s0960-894x(00)80178-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Yoshimura, Yuichi, Kazuhiro Asami, Tomozumi Imamichi, Tomoko Okuda, Kimiyasu Shiraki, and Hiroki Takahata. "Design and Synthesis of Isonucleosides Constructed on a 2-Oxa-6-thiabicyclo[3.2.0]heptane Scaffold(1)." Journal of Organic Chemistry 75, no. 12 (June 18, 2010): 4161–71. http://dx.doi.org/10.1021/jo100556u.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

FRANZISKET, L., and A. HEESING. "ChemInform Abstract: Cationic Rearrangements of 2-Azabicyclo(3.2.0)heptane Systems - NMR and MS Methods for the Analysis of 17O- or 18O-Labeled Compounds." ChemInform 23, no. 24 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199224070.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Bateson, John H., Patricia M. Roberts, Terence C. Smale, and Robert Southgate. "Olivanic acid analogues. Part 5. Synthesis of 3-alkylthio and 3-alkylsulphinyl analogues via Michael addition of thiols to 3-unsubstituted 1-azabicyclo[3.2.0]hept-2-ene-2-carboxylates. X-Ray molecular structure of (2RS,3RS,5SR)-benzyl 3-ethylthio-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylate and (2RS,3SR,5SR,6RS,1′RS)- and (2RS,3SR,5RS,6SR,1′SR)-benzyl 3-chloro-6-(1-hydroxyethyl)-7-oxo-3-[(SR)-phenylsulphinyl]-1-azabicyclo[3.2.0]heptane-2-carboxylate." J. Chem. Soc., Perkin Trans. 1, no. 6 (1990): 1541–53. http://dx.doi.org/10.1039/p19900001541.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Su, Min, and Jingkang Wang. "Molar Enthalpy of Crystallization of (2S,5R,6R)-6-Amino-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid in Aqueous Sodium Sulfate and Ammonium Sulfate Solutions†." Journal of Chemical & Engineering Data 55, no. 10 (October 14, 2010): 4546–48. http://dx.doi.org/10.1021/je100445s.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Walker, Daniel, Brian Eklov, and Matthew Bedore. "Practical Synthesis of 3-Oxa-6-azabicyclo[3.1.1]heptane Hydrotosylate; A Novel Morpholine-Based Building Block." Synthesis 44, no. 18 (July 26, 2012): 2859–62. http://dx.doi.org/10.1055/s-0032-1316748.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Theobald, F., N. Rodier, T. Lakhlifi, A. Sedqui, and B. Laude. "Structure of methyl 4,exo-6-diphenyl-exo-2,3-(phenyliminodicarbonyl)-7-azabicyclo[2.2.1]heptane-1-carboxylate." Acta Crystallographica Section C Crystal Structure Communications 46, no. 6 (June 15, 1990): 1074–77. http://dx.doi.org/10.1107/s0108270189010735.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Shiozaki, Masao, and Noboru Ishida. "Preparation and Reactions of Optically Active 6-(2,4-Dimethoxybenzyl)-2-[(1′,2′-O-isopropylidene)ethyl]-4-methoxy-3-oxa-7-oxo-6-azabicyclo[3.2.0]heptane. Syntheses of 2-Amino-2,3-dideoxy(branched-chain)sugar Analogues." Chemistry Letters 16, no. 7 (July 5, 1987): 1403–6. http://dx.doi.org/10.1246/cl.1987.1403.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

SANO, T., Y. HORIGUCHI, S. KAMBE, K. TANAKA, J. TAGA, J. TODA, and Y. TSUDA. "ChemInform Abstract: Dioxopyrrolines. Part 47. Thermal Rearrangements of 7-Vinyl Derivatives of 1-Aryl-5-ethoxycarbonyl-2-azabicyclo(3.2.0)heptane-3,4- diones and Their Imidates." ChemInform 22, no. 1 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199101103.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

SANO, Takehiro, Jun TODA, and Yoshisuke TSUDA. "Dioxopyrroline. L. Skeletal Rearrangements of 7-Vinyl-7-trimethylsilyloxy-5-ethoxycarbonyl-1-phenyl-2-azabicyclo(3.2.0)heptane-3,4-diones under Thermal, Basic, and Acidic Conditions." CHEMICAL & PHARMACEUTICAL BULLETIN 40, no. 1 (1992): 36–42. http://dx.doi.org/10.1248/cpb.40.36.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Hambalek, R. J., R. C. Hynes, and G. Just. "Structure of (±)-exo-4'-hydroxy-exo-6'-hydroxymethyl-endo-3'-thymin-1-yl-2',7'-dioxabicyclo[3.2.0]heptane." Acta Crystallographica Section C Crystal Structure Communications 49, no. 12 (December 15, 1993): 2055–56. http://dx.doi.org/10.1107/s0108270193004962.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Evans, Chris, Ray McCague, Stanley M. Roberts, Alan G. Sutherland, and Richard Wisdom. "Whole cell catalysed kinetic resolution of 6-azabicyclo[3.2.0]hept-3-en-7-one: synthesis of (–)-cispentacin (FR 109615)." J. Chem. Soc., Perkin Trans. 1, no. 9 (1991): 2276–77. http://dx.doi.org/10.1039/p19910002276.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

SAKAI, T., Y. KIMURA, K. KITASAKA, S. TSUBOI, M. UTAKA, and K. SOMEKAWA. "ChemInform Abstract: Synthesis of Highly Optically Active (-)-endo-6-Acetoxy-3-azabicyclo(3, 2,0)heptane-2,4-dione." ChemInform 24, no. 17 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199317154.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Semchenko, F. M., O. I. Lukashov, P. V. Kazakov, N. S. Mirzabekova, and M. I. Vlasov. "Preparative-Scale Production of the Analgesic (2R*)-2-(6′-Chloropyridin-3-yl)-7-Azabicyclo[2.2.1]Heptane (Epibatidine)." Pharmaceutical Chemistry Journal 47, no. 8 (November 2013): 437–41. http://dx.doi.org/10.1007/s11094-013-0976-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Qin, Changyong, and Steven R. Davis. "Thermal Isomerization of Tricyclo[4.1.0.02,7]heptane and Bicyclo[3.2.0]hept-6-ene through the (E,Z)-1,3-Cycloheptadiene Intermediate." Journal of Organic Chemistry 68, no. 23 (November 2003): 9081–87. http://dx.doi.org/10.1021/jo035168s.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Francisco, Cosme G., Antonio J. Herrera, and Ernesto Suárez. "Intramolecular hydrogen abstraction promoted by N-radicals: synthesis of chiral 7-oxa-2-azabicyclo[2.2.1]heptane and 8-oxa-6-azabicyclo[3.2.1]octane ring systems." Tetrahedron: Asymmetry 11, no. 19 (October 2000): 3879–82. http://dx.doi.org/10.1016/s0957-4166(00)00364-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Micheli, Fabrizio, Paolo Cavanni, Daniele Andreotti, Roberto Arban, Roberto Benedetti, Barbara Bertani, Michela Bettati, et al. "6-(3,4-Dichlorophenyl)-1-[(Methyloxy)methyl]-3-azabicyclo[4.1.0]heptane: A New Potent and Selective Triple Reuptake Inhibitor." Journal of Medicinal Chemistry 53, no. 13 (July 8, 2010): 4989–5001. http://dx.doi.org/10.1021/jm100481d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

HAMBALEK, R. J., R. C. HYNES, and G. JUST. "ChemInform Abstract: Structure of (.+-.)-exo-4′-Hydroxy-exo-6′-hydroxymethyl-endo-3′-thymin- 1-yl-2′,7′-dioxabicyclo(3.2.0)heptane." ChemInform 25, no. 13 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199413252.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Singh, Rajinder, and R. D. G. Cooper. "Synthesis and biological evaluation of 6-azabicyclo[3.2.0]hept-2-ene derivatives as potential anti-bacterial agents and β-lactamase inhibitors." Tetrahedron 50, no. 42 (January 1994): 12049–64. http://dx.doi.org/10.1016/s0040-4020(01)89559-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!