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  1. Article ; Online: Enantioselective synthesis of atropisomeric indoles via iron-catalysed oxidative cross-coupling.

    Surgenor, Richard R / Liu, Xiangqian / Keenlyside, Morgan J H / Myers, William / Smith, Martin D

    Nature chemistry

    2022  Volume 15, Issue 3, Page(s) 357–365

    Abstract: Heterobiaryl compounds that exhibit axial chirality are of increasing value and interest across several fields, but direct oxidative methods for their enantioselective synthesis remain elusive. Here we disclose that an iron catalyst in the presence of a ... ...

    Abstract Heterobiaryl compounds that exhibit axial chirality are of increasing value and interest across several fields, but direct oxidative methods for their enantioselective synthesis remain elusive. Here we disclose that an iron catalyst in the presence of a chiral PyBOX ligand and an oxidant enables direct coupling between naphthols and indoles to yield atropisomeric heterobiaryl compounds with high levels of enantioselectivity. The reaction exhibits remarkable chemoselectivity and exclusively yields cross-coupled products without competing homocoupling. Mechanistic investigations enable us to postulate that an indole radical is generated in the reaction but that this is probably an off-cycle event, and that the reaction proceeds through formation of a chiral Fe-bound naphthoxy radical that is trapped by a nucleophilic indole. We envision that this simple, cheap and sustainable catalytic manifold will facilitate access to a range of heterobiaryl compounds and enable their application across the fields of materials science, medicinal chemistry and catalysis.
    Language English
    Publishing date 2022-12-12
    Publishing country England
    Document type Journal Article
    ZDB-ID 2464596-5
    ISSN 1755-4349 ; 1755-4330
    ISSN (online) 1755-4349
    ISSN 1755-4330
    DOI 10.1038/s41557-022-01095-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Convergent and Stereoselective Method for the Synthesis of Acyclic α-Chloroenamides

    Surgenor, Richard R. / Grote, Andrea C. / McGeough, Catherine / Narayanan, Arjun / Wang, Wenyu / Collier, Philip N.

    Journal of organic chemistry. 2020 Oct. 12, v. 85, no. 21

    2020  

    Abstract: A direct, stereocontrolled synthesis of acyclic α-chloroenamides is presented. Our methodology showed good yields and substrate scope. Mechanistic insights are provided that account for the high levels of stereoselectivity reported. Subsequent synthetic ... ...

    Abstract A direct, stereocontrolled synthesis of acyclic α-chloroenamides is presented. Our methodology showed good yields and substrate scope. Mechanistic insights are provided that account for the high levels of stereoselectivity reported. Subsequent synthetic manipulation of the α-chloroenamides provides direct entry to polyfunctionalized acyclic enamides, compounds of wide use in organic chemistry and the pharmaceutical industry.
    Keywords organic chemistry ; pharmaceutical industry ; stereoselective synthesis ; stereoselectivity
    Language English
    Dates of publication 2020-1012
    Size p. 14158-14165.
    Publishing place American Chemical Society
    Document type Article
    ZDB-ID 123490-0
    ISSN 1520-6904 ; 0022-3263
    ISSN (online) 1520-6904
    ISSN 0022-3263
    DOI 10.1021/acs.joc.0c01370
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: Convergent and Stereoselective Method for the Synthesis of Acyclic α-Chloroenamides.

    Surgenor, Richard R / Grote, Andrea C / McGeough, Catherine / Narayanan, Arjun / Wang, Wenyu / Collier, Philip N

    The Journal of organic chemistry

    2020  Volume 85, Issue 21, Page(s) 14158–14165

    Abstract: A direct, stereocontrolled synthesis of acyclic α-chloroenamides is presented. Our methodology showed good yields and substrate scope. Mechanistic insights are provided that account for the high levels of stereoselectivity reported. Subsequent synthetic ... ...

    Abstract A direct, stereocontrolled synthesis of acyclic α-chloroenamides is presented. Our methodology showed good yields and substrate scope. Mechanistic insights are provided that account for the high levels of stereoselectivity reported. Subsequent synthetic manipulation of the α-chloroenamides provides direct entry to polyfunctionalized acyclic enamides, compounds of wide use in organic chemistry and the pharmaceutical industry.
    Language English
    Publishing date 2020-10-12
    Publishing country United States
    Document type Journal Article
    ZDB-ID 123490-0
    ISSN 1520-6904 ; 0022-3263
    ISSN (online) 1520-6904
    ISSN 0022-3263
    DOI 10.1021/acs.joc.0c01370
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Total Synthesis and Stereochemical Assignment of the Antimicrobial Lipopeptide Cerexin A1

    Cochrane, Stephen A / Surgenor Richard R / Khey Kevin M. W / Vederas John C

    Organic letters. 2015 Nov. 06, v. 17, no. 21

    2015  

    Abstract: The isolation and total synthesis of the antimicrobial lipopeptide cerexin A₁ is reported. This synthesis includes the preparation of orthogonally protected γ-hydroxylysine, utilizing a nitrile Reformatsky-type reaction as a key step to yield both ... ...

    Abstract The isolation and total synthesis of the antimicrobial lipopeptide cerexin A₁ is reported. This synthesis includes the preparation of orthogonally protected γ-hydroxylysine, utilizing a nitrile Reformatsky-type reaction as a key step to yield both diastereomers more efficiently than previously reported methods. The configuration of the β-hydroxyl in the lipid tail was determined by the use of a modified Ohrui–Akasaka approach. Furthermore, new cerexin analogues from Bacillus mycoides ATCC 21929 were isolated and characterized, revealing an ε-amino succinylation of a hydroxylysine residue that is unusual in a nonribosomal peptide synthetase product.
    Keywords Bacillus mycoides ; chemical reactions ; diastereomers ; hydroxylysine ; lipopeptides ; organic compounds ; stereochemistry
    Language English
    Dates of publication 2015-1106
    Size p. 5428-5431.
    Publishing place American Chemical Society
    Document type Article
    ISSN 1523-7052
    DOI 10.1021%2Facs.orglett.5b02779
    Database NAL-Catalogue (AGRICOLA)

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  5. Article ; Online: Total Synthesis and Stereochemical Assignment of the Antimicrobial Lipopeptide Cerexin A1.

    Cochrane, Stephen A / Surgenor, Richard R / Khey, Kevin M W / Vederas, John C

    Organic letters

    2015  Volume 17, Issue 21, Page(s) 5428–5431

    Abstract: The isolation and total synthesis of the antimicrobial lipopeptide cerexin A1 is reported. This synthesis includes the preparation of orthogonally protected γ-hydroxylysine, utilizing a nitrile Reformatsky-type reaction as a key step to yield both ... ...

    Abstract The isolation and total synthesis of the antimicrobial lipopeptide cerexin A1 is reported. This synthesis includes the preparation of orthogonally protected γ-hydroxylysine, utilizing a nitrile Reformatsky-type reaction as a key step to yield both diastereomers more efficiently than previously reported methods. The configuration of the β-hydroxyl in the lipid tail was determined by the use of a modified Ohrui-Akasaka approach. Furthermore, new cerexin analogues from Bacillus mycoides ATCC 21929 were isolated and characterized, revealing an ε-amino succinylation of a hydroxylysine residue that is unusual in a nonribosomal peptide synthetase product.
    MeSH term(s) Anti-Bacterial Agents/chemical synthesis ; Anti-Bacterial Agents/chemistry ; Anti-Bacterial Agents/pharmacology ; Anti-Infective Agents ; Bacillus cereus/chemistry ; Molecular Structure ; Peptides/chemical synthesis ; Peptides/chemistry ; Peptides/pharmacology
    Chemical Substances Anti-Bacterial Agents ; Anti-Infective Agents ; Peptides ; cerexins (65454-17-3)
    Language English
    Publishing date 2015-11-06
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1523-7052
    ISSN (online) 1523-7052
    DOI 10.1021/acs.orglett.5b02779
    Database MEDical Literature Analysis and Retrieval System OnLINE

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