Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sureeporn Ruengsangtongkul"'
Autor:
Kunlayanee Punjajom, Sureeporn Ruengsangtongkul, Jumreang Tummatorn, Praneet Paiboonsombat, Somsak Ruchirawat, Charnsak Thongsornkleeb
Publikováno v:
The Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f9d5520698e1a29ae6f849a96d42dd5
https://doi.org/10.1021/acs.joc.3c00027
https://doi.org/10.1021/acs.joc.3c00027
Autor:
Charnsak Thongsornkleeb, Sureeporn Ruengsangtongkul, Takahito Kuribara, Nattawadee Chaisan, Jumreang Tummatorn, Somsak Ruchirawat
Publikováno v:
Synlett. 33:1329-1334
Unsymmetrical 1,1,2-triacylalkenes were conveniently prepared by the oxidative coupling of 1,3-keto esters with terminal alkynes by employing 4.0 equivalents of inexpensive ceric ammonium nitrate (CAN) as the oxidant in acetonitrile as the solvent at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5578187714583cb39613d82afb85d949
https://doi.org/10.1055/a-1774-6966
https://doi.org/10.1055/a-1774-6966
Autor:
Charnsak Thongsornkleeb, Nattawadee Chaisan, Sureeporn Ruengsangtongkul, Jumreang Tummatorn, Somsak Ruchirawat
Publikováno v:
Synlett. 33:1426-1430
A mild and convenient method for the synthesis of 2,2-dihaloketones and gem-dihalolactols has been developed. For the synthesis of 2,2-dihaloketones, alkynes were employed as substrates to react with halogenating agents, Cl2 or ClBr, that were genera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7fff9f26d224ad576e51c58be3f1704
https://doi.org/10.1055/a-1774-7077
https://doi.org/10.1055/a-1774-7077
Autor:
Sureeporn Ruengsangtongkul, Jumreang Tummatorn, Nattawadee Chaisan, Kittipong Chainok, Somsak Ruchirawat, Charnsak Thongsornkleeb
Publikováno v:
The Journal of Organic Chemistry. 86:4671-4698
The combination of catalytic aqueous hydrochloric acid (HCl) and N-bromosuccinimide (NBS) generated electrophilic bromine monochloride (BrCl), which readily induced spiroannulation of 2-alkynolyl anilides (n = 1-3) to form gem-dibromospirocyclic benz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d676d4e4f041c5b9fa2bd6039543f8f0
https://doi.org/10.1021/acs.joc.1c00086
https://doi.org/10.1021/acs.joc.1c00086
Autor:
Somsak Ruchirawat, Sureeporn Ruengsangtongkul, Jumreang Tummatorn, Kanyapat Lumyong, Charnsak Thongsornkleeb, Kunlayanee Punjajom, Phongprapan Nimnual, Warabhorn Rodphon, Nattawadee Chaisan
Publikováno v:
Organic Letters. 21:4694-4697
1,1-Disubstituted vinyl triflates are synthesized by direct hydrotriflation of terminal alkynes employing a combination of TfOH and TMSN3 in DCM at room temperature. Interestingly, under these cond...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb5760750bdfb404c0a4437652788da5
https://doi.org/10.1021/acs.orglett.9b01576
https://doi.org/10.1021/acs.orglett.9b01576
Autor:
Somsak Ruchirawat, Sureeporn Ruengsangtongkul, Nattawadee Chaisan, Jumreang Tummatorn, Charnsak Thongsornkleeb
Publikováno v:
Organic Letters. 21:2514-2517
Stoichiometric ceric ammonium nitrate (CAN) and a catalytic amount of Pd(PPh3)2Cl2 (5 mol %) can rapidly produce multisubstituted 2-ketofuran-4-carboxylate esters from 2-propargylic 1,3-ketoesters via oxidative O-cyclization reaction. Pd(PPh3)2Cl2 wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::133474c4f52ce4cf1c869aaff24e9b18
https://doi.org/10.1021/acs.orglett.9b00053
https://doi.org/10.1021/acs.orglett.9b00053
Autor:
Nattawadee, Chaisan, Sureeporn, Ruengsangtongkul, Jumreang, Tummatorn, Somsak, Ruchirawat, Kittipong, Chainok, Charnsak, Thongsornkleeb
Publikováno v:
The Journal of organic chemistry. 86(6)
The combination of catalytic aqueous hydrochloric acid (HCl) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6c8750da321b0374052fc508c14e29a5
https://pubmed.ncbi.nlm.nih.gov/33689323
https://pubmed.ncbi.nlm.nih.gov/33689323
Autor:
Nattawadee Chaisan, Jumreang Tummatorn, Sureeporn Ruengsangtongkul, Wilailak Kaewsri, Krissada Norseeda, Charnsak Thongsornkleeb, Somsak Ruchirawat
Publikováno v:
Asian Journal of Organic Chemistry. 7:203-211
A method for the TfOH-promoted (Tf=trifluoromethanesulfonyl) cyclization of alkyne-tethered 1,3-ketoesters to afford 2-cyclohexenone-2-carboxylate derivatives has been developed. The procedure requires no transition-metal reagent or catalyst and is p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c94c146e75dcd075014c5d644a66d439
https://doi.org/10.1002/ajoc.201700510
https://doi.org/10.1002/ajoc.201700510
Autor:
Jumreang, Tummatorn, Kunlayanee, Punjajom, Warabhorn, Rodphon, Sureeporn, Ruengsangtongkul, Nattawadee, Chaisan, Kanyapat, Lumyong, Charnsak, Thongsornkleeb, Phongprapan, Nimnual, Somsak, Ruchirawat
Publikováno v:
Organic letters. 21(12)
1,1-Disubstituted vinyl triflates are synthesized by direct hydrotriflation of terminal alkynes employing a combination of TfOH and TMSN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2d14f66c1aeb8431b1099f3f5a0b92c3
https://pubmed.ncbi.nlm.nih.gov/31184914
https://pubmed.ncbi.nlm.nih.gov/31184914
Autor:
Sureeporn, Ruengsangtongkul, Nattawadee, Chaisan, Charnsak, Thongsornkleeb, Jumreang, Tummatorn, Somsak, Ruchirawat
Publikováno v:
Organic letters. 21(8)
Stoichiometric ceric ammonium nitrate (CAN) and a catalytic amount of Pd(PPh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eaae2a091af3ad8220652b792ab49459
https://pubmed.ncbi.nlm.nih.gov/30816716
https://pubmed.ncbi.nlm.nih.gov/30816716