دورية أكاديمية

Copper-Catalyzed Synthesis of Masked (Hetero)Aryl Sulfinates.

التفاصيل البيبلوغرافية
العنوان: Copper-Catalyzed Synthesis of Masked (Hetero)Aryl Sulfinates.
المؤلفون: Merino MR; Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford OX1 3TA, U.K., Cook XAF; Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford OX1 3TA, U.K., Blakemore DC; Medicine Design, Pfizer Inc., Eastern Point Road, Groton, Connecticut 06340, United States., Moses IB; Pharmaceutical Sciences, Pfizer Inc., Discovery Park, Ramsgate Road, Kent CT13 9ND, U.K., Sach NW; Medicine Design, La Jolla Laboratories, Pfizer Inc., 10777 Science Center Drive, San Diego, California 92121, United States., Shavnya A; Medicine Design, Pfizer Inc., Eastern Point Road, Groton, Connecticut 06340, United States., Willis MC; Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford OX1 3TA, U.K.
المصدر: Organic letters [Org Lett] 2024 Apr 12; Vol. 26 (14), pp. 2817-2820. Date of Electronic Publication: 2024 Jan 08.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: American Chemical Society Country of Publication: United States NLM ID: 100890393 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1523-7052 (Electronic) Linking ISSN: 15237052 NLM ISO Abbreviation: Org Lett Subsets: PubMed not MEDLINE; MEDLINE
أسماء مطبوعة: Original Publication: Washington, DC : American Chemical Society, c1999-
مستخلص: Catalysis using substoichiometric copper facilitates the synthesis of masked (hetero)aryl sulfinates under mild, base-free conditions from aryl iodides and the commercial sulfonylation reagent sodium 1-methyl 3-sulfinopropanoate (SMOPS). The development of a tert -butyl ester variant of the SMOPS reagent allowed the use of aryl bromide substrates. The sulfones thus generated can be unmasked and functionalized in situ to form a variety of sulfonyl-containing functional groups.
References: J Am Chem Soc. 2015 Aug 5;137(30):9571-4. (PMID: 26177230)
Org Biomol Chem. 2014 Dec 28;12(48):9743-59. (PMID: 25354469)
Chem Commun (Camb). 2020 Apr 14;56(30):4145-4155. (PMID: 32242574)
Chem Sci. 2017 Jun 1;8(6):4437-4442. (PMID: 28936330)
Bioconjug Chem. 2023 Sep 20;34(9):1679-1687. (PMID: 37657082)
Org Lett. 2011 Sep 16;13(18):4876-8. (PMID: 21866926)
J Org Chem. 2018 Jun 15;83(12):6589-6598. (PMID: 29786439)
Chem Rev. 2012 Mar 14;112(3):1650-80. (PMID: 22107104)
J Am Chem Soc. 2020 May 13;142(19):8972-8979. (PMID: 32302104)
Chem Asian J. 2022 Aug 15;17(16):e202200408. (PMID: 35644918)
Org Lett. 2017 Nov 17;19(22):6033-6035. (PMID: 29043813)
RSC Adv. 2021 Mar 1;11(16):9130-9221. (PMID: 35423435)
Org Lett. 2017 Jul 21;19(14):3819-3822. (PMID: 28670905)
J Org Chem. 2013 May 17;78(10):5022-5. (PMID: 23656304)
J Org Chem. 2012 Nov 16;77(22):10468-72. (PMID: 23113716)
Angew Chem Int Ed Engl. 2021 Oct 4;60(41):22461-22468. (PMID: 34342107)
Chem Sci. 2020 Oct 22;11(48):13071-13078. (PMID: 34094489)
J Am Chem Soc. 2018 Nov 21;140(46):15916-15923. (PMID: 30412397)
Chem Commun (Camb). 2012 Oct 14;48(80):10037-9. (PMID: 22945283)
تواريخ الأحداث: Date Created: 20240108 Latest Revision: 20240425
رمز التحديث: 20240425
مُعرف محوري في PubMed: PMC11020165
DOI: 10.1021/acs.orglett.3c03621
PMID: 38189248
قاعدة البيانات: MEDLINE
الوصف
تدمد:1523-7052
DOI:10.1021/acs.orglett.3c03621