Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Venukrishnan Komanduri"'
Publikováno v:
Organic & Biomolecular Chemistry. 21:3245-3250
The preparation of highly strained o-dialkoxyphenylene benzothiazole paracyclophane-1,9-dienes is reported and the diastereoselectivity of the ring opening metathesis investigated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2135d67e8ef5fd6191d3fd08d67bbe4
https://doi.org/10.1039/d2ob01989b
https://doi.org/10.1039/d2ob01989b
Autor:
Yurachat Janpatompong, Andrew M. Spring, Venukrishnan Komanduri, Raja U. Khan, Michael L. Turner
Publikováno v:
Janpatompong, Y, Spring, A, Komanduri, V, Khan, R & Turner, M 2022, ' Synthesis and Ring Opening Metathesis Polymerisation of o-Dialkoxy Paracyclophanedienes ', Macromolecules, vol. 55, no. 24 . https://doi.org/10.1021/acs.macromol.2c02111
The highly strained ortho-diethylhexyloxy [2.2]paracyclophane-1,9-diene (M1) can be synthesized by ring contraction of a dithial[3.3]paracyclophane using a benzyne induced Stevens rearrangement. This paracyclophanediene undergoes ring opening metathe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4746324f3e246f71342251346a178359
https://research.manchester.ac.uk/en/publications/c68b9a66-b1d8-4222-8acc-5551227e4853
https://research.manchester.ac.uk/en/publications/c68b9a66-b1d8-4222-8acc-5551227e4853
Autor:
Yurachat, Janpatompong, Andrew M, Spring, Venukrishnan, Komanduri, Raja U, Khan, Michael L, Turner
Publikováno v:
Macromolecules. 55(24)
The highly strained
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d8388d073541ad5b72c08984ddaa9377
https://pubmed.ncbi.nlm.nih.gov/36590370
https://pubmed.ncbi.nlm.nih.gov/36590370
Autor:
Yurachat Janpatompong, Michael L. Turner, Daniel J. Tate, Raymundo Marcial-Hernandez, Venukrishnan Komanduri
Publikováno v:
Komanduri, V, Janpatompong, Y, Marcial Hernández, R, Tate, D & Turner, M 2021, ' A Sequential ROMP Strategy to Donor-Acceptor Di-, Tri-and Tetra Arylenevinylene Block Copolymers ', Polymer Chemistry, no. 46, pp. 6643-6782 . https://doi.org/10.1039/D1PY01202A
The synthesis of donor–acceptor di-, tri- and tetrablock copolymers via sequential ROMP of electron rich and electron deficient paracyclophanediene monomers using Grubbs ruthenium carbene initiator, G3, is discussed. Block copolymers were initially
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee11db29b58da3bec25cbfd8a8224a22
https://doi.org/10.1039/d1py01202a
https://doi.org/10.1039/d1py01202a
Autor:
Dharam R. Kumar, Daniel J. Tate, Michael L. Turner, Venukrishnan Komanduri, Raymundo Marcial-Hernandez
Publikováno v:
Macromolecules. 52:7137-7144
Dialkoxy- and dialkyl-substituted phenylene benzothiadiazole paracyclophane-1,9-diene monomers undergo living ring-opening metathesis polymerization using ruthenium carbene initiators (G3) to give ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3739bef1febf13381bc453ea84e04cb
https://doi.org/10.1021/acs.macromol.9b01244
https://doi.org/10.1021/acs.macromol.9b01244
Autor:
Daniel J. Tate, Raymundo Marcial-Hernandez, Benjamin J. Lidster, Venukrishnan Komanduri, Michael L. Turner, Dharam R. Kumar
Publikováno v:
Komanduri, V, Kumar, D, Tate, D, Marcial Hernandez, R, Lidster, B & Turner, M 2019, ' Bidirectional ROMP of Paracylophane-1,9-dienes to Tri-and Penta-Block p-Phenylenevinylene Copolymers ', Polymer Chemistry . https://doi.org/10.1039/C9PY00147F
Dialkoxy and dialkyl substituted paracyclophane-1,9-dienes undergo bidirectional ring opening metathesis polymerisation (ROMP) on addition of bifunctional Hoveyda-Grubbs initiators. The living nature of the polymerisation was demonstrated for differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eb8df7909340e378ab494e28c143541
https://doi.org/10.1039/c9py00147f
https://doi.org/10.1039/c9py00147f
Autor:
Dharam R. Kumar, Shuzo Hirata, Benjamin J. Lidster, Takuya Yamamoto, Venukrishnan Komanduri, Shoki Matsuda, Michael L. Turner, Yasuyuki Tezuka, Martin Vacha
Publikováno v:
Chemical Science
Lidster, B, Hirata, S, Matsuda, S, Yamamoto, T, Komanduri, V, Kumar, D, Tezuka, Y, Vacha, M & Turner, M 2018, ' Macrocyclic Poly(p-phenylenevinylene)s by Ring Expansion Metathesis Polymerisation and their Characterisation by Single-Molecule Spectroscopy ', Chemical Science . https://doi.org/10.1039/C7SC03945J
Lidster, B, Hirata, S, Matsuda, S, Yamamoto, T, Komanduri, V, Kumar, D, Tezuka, Y, Vacha, M & Turner, M 2018, ' Macrocyclic Poly(p-phenylenevinylene)s by Ring Expansion Metathesis Polymerisation and their Characterisation by Single-Molecule Spectroscopy ', Chemical Science . https://doi.org/10.1039/C7SC03945J
Ring expansion metathesis polymerisation (REMP) has proven to be a viable approach to prepare high purity cyclic polymers. Macrocyclic polymers with a fully conjugated defect free backbone are of particular interest as these polymers have no end grou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2525b325606b033f8c2a75b1958b72bf
Autor:
Xiaoda Niu, W. Michael Seganish, R. Jason Herr, James P. Harding, Deen Tulshian, Larry Yet, Brian J. Lavey, Thierry O. Fischmann, Koraboina Chandra Prakash, Christopher Sondey, William J. Greenlee, Jinhai Yang, Venukrishnan Komanduri, William T. McElroy
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 25:1836-1841
Interleukin receptor-associated kinase 4 (IRAK4) is a critical element of the Toll-like/interleukin-1 receptor inflammation signaling pathway. A screening campaign identified a novel diaminopyrimidine hit that exhibits weak IRAK4 inhibitory activity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8341cb6919ca89d984827a91b91440ad
https://doi.org/10.1016/j.bmcl.2015.03.043
https://doi.org/10.1016/j.bmcl.2015.03.043
Autor:
Benjamin John, Lidster, Shuzo, Hirata, Shoki, Matsuda, Takuya, Yamamoto, Venukrishnan, Komanduri, Dharam Raj, Kumar, Yasuyuki, Tezuka, Martin, Vacha, Michael L, Turner
Publikováno v:
Chemical Science
Ring expansion metathesis polymerisation (REMP) has proven to be a viable approach to prepare high purity macrocyclic phenylenevinylene polymers.
Ring expansion metathesis polymerisation (REMP) has proven to be a viable approach to prepare high
Ring expansion metathesis polymerisation (REMP) has proven to be a viable approach to prepare high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::51d0304f293831ef3ed5d5aeae4d16bc
https://pubmed.ncbi.nlm.nih.gov/29732077
https://pubmed.ncbi.nlm.nih.gov/29732077
Autor:
Boyoung Y. Park, Khoa D. Nguyen, Mani Raj Chaulagain, Michael J. Krische, Venukrishnan Komanduri
Publikováno v:
Journal of the American Chemical Society
The cationic ruthenium catalyst generated upon the acid-base reaction of H2Ru(CO)(PPh3)3 and 2,4,6-(2-Pr)3PhSO3H promotes the redox-triggered C-C coupling of 2-alkynes and primary alcohols to form (Z)-homoallylic alcohols with good to complete contro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d4def575101b82b95fe096fa4f38ac3
https://doi.org/10.1021/ja505962w
https://doi.org/10.1021/ja505962w