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  1. Article ; Online: The genus Contracaecum Raillet & Henry (Nematoda: Anisakidae): host and geographical distribution on Neotropical and Antarctic species.

    Garbin, Lucas E / Diaz, Julia I / Servián, Andrea / Fusaro, Bruno / Navone, Graciela T

    Zootaxa

    2023  Volume 5256, Issue 1, Page(s) 43–62

    Abstract: Nematodes of the genus Contracaecum Raillet & Henry, 1912 (Anisakidae, Contracaecinae) have ...

    Abstract Nematodes of the genus Contracaecum Raillet & Henry, 1912 (Anisakidae, Contracaecinae) have a worldwide distribution. The taxonomy of the genus Contracaecum is well-known nowadays due to several morphometric studies, scanning electron microscopy, and molecular biology. The aim of this work was to review, clarify, and summarize the valid species of the genus Contracaecum parasitizing piscivorous sea birds and mammals from both the Neotropical and Antarctic regions reviewing all scientific available papers and electronic searching data up to date. A checklist on Neotropical and Antarctic Contracaecum spp. was organized through a revision of scientific papers and original descriptions. The systematic online search and the most updated papers were obtained through SCOPUS, Google Scholar, PubMed, Medline, World Register of Marine Species, etc. We provide information about hosts, Neotropical and Antarctic localities where worms were collected, references, molecular markers, and Genbank accession numbers. Twenty-five Neotropical and Antarctic Contracaecum species have been recorded up to date and checked out as valid ones according to the most updated data. Twenty-one species parasitize exclusively fish-eating birds, two species were reported only on marine mammals, and the other two parasitize both sea birds and mammals. A total of 20 Contracaecum species are exclusively reported for the Neotropical region, three only for Antarctic hosts, and two species were reported parasitizing both Neotropical and Antarctic hosts. Several Contracaecum species (10) have been corroborated by molecular analysis of different genetic markers. After reviewing all morphological descriptions of the Contracaecum species, and despite most of them have been characterized only by morphometric methods, we are convinced that all species listed in this work correspond to good and valid Contracaecum Neotropical and Antarctic species. Present results indicate that more taxonomic and molecular studies are needed to advance the understanding of the distribution and host specificity of the Contracaecum species.
    MeSH term(s) Animals ; Antarctic Regions ; Ascaridida Infections/veterinary ; Bird Diseases ; Ascaridoidea/anatomy & histology ; Ascaridoidea/genetics ; Birds ; Mammals
    Language English
    Publishing date 2023-03-16
    Publishing country New Zealand
    Document type Journal Article
    ISSN 1175-5334
    ISSN (online) 1175-5334
    DOI 10.11646/zootaxa.5256.1.3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The Relationship of William Henry Perkin, Jr. and Sir Robert Robinson: Teacher and Student, then Student and Teacher.

    Seeman, Jeffrey I

    Chemistry (Weinheim an der Bergstrasse, Germany)

    2020  Volume 27, Issue 5, Page(s) 1576–1591

    Abstract: William Henry Perkin, Jr. FRS, the son of the inventor of mauve and other commercial dyes and ...

    Abstract William Henry Perkin, Jr. FRS, the son of the inventor of mauve and other commercial dyes and credited for initiating the industrialization of chemistry, was himself a notable chemist. He was the Professor of Organic Chemistry at Manchester from 1892-1912 and then was the Waynflete Professor of Chemistry at Oxford and the first Head of the Dyson Perrins Laboratory from 1912-1929. One of Perkin's graduate students and research assistants at Manchester was Robert Robinson, subsequently Sir Robert Robinson, FRS and recipient of the 1947 Nobel Prize in Chemistry. Perkin and Robinson had perhaps the most productive and broad collaboration between a professor and one's student. Together, during and after Robinson's student days, they had 71 joint publications, 25 of which involved just the two of them, 17 of which involved the structure determination of strychnine, and eight of which were published after Perkin's death in 1929. Upon Perkin's early death, Robinson succeeded him as the fourth Waynflete Professor of Chemistry at the Dyson Perrins Laboratory, Oxford University. This Essay will examine the professional relationship of Perkin, Jr. and Robinson as revealed in their joint publications on the structure of strychnine.
    Language English
    Publishing date 2020-12-29
    Publishing country Germany
    Document type Journal Article ; Review
    ZDB-ID 1478547-X
    ISSN 1521-3765 ; 0947-6539
    ISSN (online) 1521-3765
    ISSN 0947-6539
    DOI 10.1002/chem.202002924
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Formal (4+1) Cycloaddition and Enantioselective Michael-Henry Cascade Reactions To Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles.

    Huang, Ji-Rong / Sohail, Muhammad / Taniguchi, Tohru / Monde, Kenji / Tanaka, Fujie

    Angewandte Chemie (International ed. in English)

    2017  Volume 56, Issue 21, Page(s) 5853–5857

    Abstract: ... oxindole-functionalized spiro[4,5]decanes and organocatalytic enantioselective Michael-Henry cascade ...

    Abstract Spiro[4,5]decanes and polycyclic compounds bearing spiro[4,5]decane systems are important biofunctional molecules. Described are diastereoselective formal (4+1) cycloaddition reactions to afford oxindole-functionalized spiro[4,5]decanes and organocatalytic enantioselective Michael-Henry cascade reactions of the (4+1) cycloaddition products to generate spirooxindole polycyclic derivatives bearing the spiro[4,5]decane system. Spiro[4,5]decanes bearing oxindoles containing three stereogenic centers and spirooxindole polycycles having seven stereogenic centers, including two all-carbon chiral quaternary centers and one tetrasubstituted chiral carbon center, were obtained with high diastereo- and enantioselectivities.
    Language English
    Publishing date 2017-04-11
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2011836-3
    ISSN 1521-3773 ; 1433-7851
    ISSN (online) 1521-3773
    ISSN 1433-7851
    DOI 10.1002/anie.201701049
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Bis(oxazoline)-based coordination polymers: a recoverable system for enantioselective Henry reactions.

    Angulo, Beatriz / García, José I / Herrerías, Clara I / Mayoral, José A / Miñana, Ana C

    The Journal of organic chemistry

    2012  Volume 77, Issue 13, Page(s) 5525–5532

    Abstract: ... in the Henry reaction is described. This strategy is based on the precipitation of an insoluble coordination ...

    Abstract An efficient release-capture strategy for the recovery and reuse of enantioselective catalysts in the Henry reaction is described. This strategy is based on the precipitation of an insoluble coordination polymer at the end of each reaction, allowing easy separation from products. The coordination polymer is formed through aggregation of Cu(II) ions with ditopic bisoxazoline-based chiral ligands. Up to 11 catalytic cycles have been conducted keeping good yields and enantioselectivities.
    MeSH term(s) Aldehydes/chemistry ; Catalysis ; Copper/chemistry ; Ligands ; Molecular Structure ; Nitro Compounds/chemical synthesis ; Nitro Compounds/chemistry ; Organometallic Compounds/chemical synthesis ; Organometallic Compounds/chemistry ; Oxazoles/chemistry ; Polymers/chemical synthesis ; Polymers/chemistry ; Stereoisomerism
    Chemical Substances Aldehydes ; Ligands ; Nitro Compounds ; Organometallic Compounds ; Oxazoles ; Polymers ; Copper (789U1901C5)
    Language English
    Publishing date 2012-07-06
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 123490-0
    ISSN 1520-6904 ; 0022-3263
    ISSN (online) 1520-6904
    ISSN 0022-3263
    DOI 10.1021/jo3005974
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: d-Mannitol-derived novel chiral thioureas: Synthesis and application in asymmetric Henry reactions

    Liu, Miaoxi / Ji, Nan / Wang, Li / Liu, Peng / He, Wei

    Tetrahedron letters. 2018 Mar. 14, v. 59, no. 11 p.999-1004

    2018  

    Abstract: ... as starting material and applied as catalysts in the asymmetric Henry reaction. Using catalyst 7a, (1S,2R)-2-nitro-1 ...

    Abstract Five novel thioureas have been obtained through multi-step reactions from d-Mannitol as starting material and applied as catalysts in the asymmetric Henry reaction. Using catalyst 7a, (1S,2R)-2-nitro-1-phenylpropan-1-ol containing two chiral centers was obtained in high yield and with high selectivity (up to 95% yield, 87% ee, 91:9 dr). This catalyst also retained activity in the presence of water, affording a up to 93% yield, 88% ee, and 94:6 dr.
    Keywords catalysts ; chemical reactions ; chemical structure ; mannitol ; Asymmetric catalysis ; Oxaziridination ; Cinchonaalkaloids ; Organic catalysis
    Language English
    Dates of publication 2018-0314
    Size p. 999-1004.
    Publishing place Elsevier Ltd
    Document type Article ; Online
    ZDB-ID 204287-3
    ISSN 1873-3581 ; 0040-4039
    ISSN (online) 1873-3581
    ISSN 0040-4039
    DOI 10.1016/j.tetlet.2018.01.082
    Database NAL-Catalogue (AGRICOLA)

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  6. Article ; Online: Polytopic bis(oxazoline)-based ligands for recoverable catalytic systems applied to the enantioselective Henry reaction.

    Angulo, Beatriz / García, José I / Herrerías, Clara I / Mayoral, José A / Miñana, Ana C

    Organic & biomolecular chemistry

    2015  Volume 13, Issue 35, Page(s) 9314–9322

    Abstract: ... catalytic systems for the Henry reaction. The results obtained with the different ligands are, in general ...

    Abstract Several kinds of polytopic chiral ligands (including ditopic, tritopic and tetratopic), based on the bis(oxazoline) and azabis(oxazoline) motifs, have been tested in the preparation of recoverable catalytic systems for the Henry reaction. The results obtained with the different ligands are, in general, good, but they point to the existence of a delicate balance between the coordinating ability of the ligand, the catalytic activity and the recovery of the catalyst by formation of the coordination polymer, related to the easiness to form oligomeric species in solution.
    Language English
    Publishing date 2015-09-21
    Publishing country England
    Document type Journal Article
    ZDB-ID 2097583-1
    ISSN 1477-0539 ; 1477-0520
    ISSN (online) 1477-0539
    ISSN 1477-0520
    DOI 10.1039/c5ob01033k
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Design Aspects of Metal-Free Nitrogen-Based Catalysts and Their Influence on the Yield in the Henry Reaction

    Yao, Qiong Ji / Khong, Duc Thinh / Gao, Qi / Judeh, Zaher M. A.

    Synthesis

    2014  Volume 46, Issue 13, Page(s) 1793–1801

    Abstract: Design aspects of metal-free nitrogen-based catalysts and their influence on the yield in the Henry ...

    Abstract Design aspects of metal-free nitrogen-based catalysts and their influence on the yield in the Henry reaction are disclosed. C 1 -Symmetric, N N -1,2-disposed amine-imine type catalysts were found to be most efficient. C 1 N N -1,2-Disposed 1,2,3,4-tetrahydro-1,1′-biisoquinoline selectively and efficiently catalyzed the addition of nitromethane to α-keto esters and aldehydes giving exclusively the corresponding β-nitro alcohol adducts in excellent yields under very mild conditions.
    Keywords catalyst design ; biisoquinoline ; C–C bond formation ; Henry reaction ; Proton Sponge
    Language English
    Publishing date 2014-04-17
    Publisher © Georg Thieme Verlag
    Publishing place Stuttgart ; New York
    Document type Article
    ZDB-ID 2033062-5
    ISSN 1437-210X ; 0039-7881
    ISSN (online) 1437-210X
    ISSN 0039-7881
    DOI 10.1055/s-0033-1341125
    Database Thieme publisher's database

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  8. Article ; Online: Construction of chiral quaternary carbon center via catalytic asymmetric aza-Henry reaction with α-substituted nitroacetates

    Li, Minghua / Ji, Nan / Lan, Ting / He, Wei / Liu, Rui

    RSC advances. 2014 May 07, v. 4, no. 39 p.20346-20350

    2014  

    Abstract: The catalytic enantioselective aza-Henry reaction of N-Boc aldimines 2 and 2-nitropropionic acid ...

    Abstract The catalytic enantioselective aza-Henry reaction of N-Boc aldimines 2 and 2-nitropropionic acid ethyl ester 3 in the mixed solvents of toluene–saturated brine (10 : 1) was catalyzed by cinchona quaternary ammonium salts to form a new quaternary carbon center. High yields (up to 90%), and excellent enantioselectivities (up to 99% ee) and diastereoselectivity ratio (up to 22 : 1) were successfully obtained with mild conditions.
    Keywords Cinchona ; aldimines ; ammonium salts ; carbon ; catalytic activity ; diastereoselectivity ; enantioselectivity ; quaternary ammonium compounds ; solvents
    Language English
    Dates of publication 2014-0507
    Size p. 20346-20350.
    Publishing place The Royal Society of Chemistry
    Document type Article ; Online
    ISSN 2046-2069
    DOI 10.1039/c4ra01390e
    Database NAL-Catalogue (AGRICOLA)

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  9. Article ; Online: The Henry reaction of (1R)-(1,4:3,6-dianhydro-D-mannitol-2-yl)-1,4:3,6-dianhydro-D-fructose 5,5'-dinitrate. Different reactive features of nitromethane to nitroethane.

    Liu, Feng-Wu / Wang, Zhen-Ji / Song, Xiao-Ping / Zhang, Sai-Yang / Liu, Hong-Min

    Carbohydrate research

    2009  Volume 344, Issue 18, Page(s) 2439–2443

    Abstract: Henry reactions of a novel higher sugar derivative, (1R)-(1,4:3,6-dianhydro-D-mannitol-2-yl)-1,4:3 ...

    Abstract Henry reactions of a novel higher sugar derivative, (1R)-(1,4:3,6-dianhydro-D-mannitol-2-yl)-1,4:3,6-dianhydro-D-fructose 5,5'-dinitrate (Alternate nomenclature: (1R)-(isomannid-2-yl)-1,4:3,6-dianhydro-D-fructose 5,5'-dinitrate), with nitromethane and nitroethane were studied. The kinetic and thermodynamic reactions with nitromethane under different conditions were carried out to afford (2S)- and (2R)-beta-nitroalcohols, respectively. But when using nitroethane the reaction gave a (2S)-beta-nitroalcohol with an inverted configuration at vicinal carbon C-1. Two stereogenic centers were generated, and one was altered in the reaction.
    MeSH term(s) Alcohols/chemical synthesis ; Carbohydrates/chemistry ; Ethane/analogs & derivatives ; Ethane/chemistry ; Kinetics ; Methane/analogs & derivatives ; Methane/chemistry ; Nitroparaffins/chemistry ; Stereoisomerism ; Thermodynamics
    Chemical Substances Alcohols ; Carbohydrates ; Nitroparaffins ; nitroethane (6KEL3ZAU0V) ; Ethane (L99N5N533T) ; Methane (OP0UW79H66) ; nitromethane (RU5WG8C3F4)
    Language English
    Publishing date 2009-12-14
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1435-7
    ISSN 1873-426X ; 0008-6215
    ISSN (online) 1873-426X
    ISSN 0008-6215
    DOI 10.1016/j.carres.2009.09.028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Quality circles--the Henry Ford Hospital experience.

    Dutkewych, J I / Buback, K

    Dimensions in health service

    1982  Volume 59, Issue 12, Page(s) 20–22

    MeSH term(s) Cost Control ; Hospital Bed Capacity, 500 and over ; Hospital Departments/standards ; Michigan ; Organizational Innovation ; Personnel Administration, Hospital/methods ; Pilot Projects ; Quality Control
    Language English
    Publishing date 1982-12
    Publishing country Canada
    Document type Journal Article
    ZDB-ID 194947-0
    ISSN 0317-7645
    ISSN 0317-7645
    Database MEDical Literature Analysis and Retrieval System OnLINE

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