Electronic Resource

Diastereodivergent Synthesis of 2‑Ene-1,4-hydroxy Sulfides from 2‑Sulfinyl Dienes via Tandem Sulfa-Michael/Sulfoxide-Sulfenate Rearrangement

التفاصيل البيبلوغرافية
العنوان: Diastereodivergent Synthesis of 2‑Ene-1,4-hydroxy Sulfides from 2‑Sulfinyl Dienes via Tandem Sulfa-Michael/Sulfoxide-Sulfenate Rearrangement
المؤلفون: Ministerio de Economía y Competitividad (España), Fernández de la Pradilla, Roberto [0000-0002-6633-8499], Viso, Alma [0000-0003- 2622-4777], Velado, Marina, Fernández de la Pradilla, Roberto, Viso, Alma
بيانات النشر: American Chemical Society 2021
نوع الوثيقة: Electronic Resource
مستخلص: The highly diastereoselective sulfa-Michael addition of thiolates to enantiopure 2-sulfinyl dienes leads to anti or syn 2- ene-1,4-hydroxy sulfides in good yields and selectivities dependent on the reaction conditions in a diastereodivergent process. Synthetic applications of these enantiopure hydroxy sulfides by subsequent sigmatropic rearrangements have been outlined.
مصطلحات الفهرس: artículo
URL: http://hdl.handle.net/10261/232257
https://doi.org/10.1021/acs.orglett.0c03929
Postprint
https://doi.org/10.1021/acs.orglett.0c03929
Sí
info:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2016-77555-C2-2-R
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-107380GB-100
الاتاحة: Open access content. Open access content
openAccess
ملاحظة: English
Other Numbers: CTK oai:digital.csic.es:10261/232257
Organic Letters 23 : 202−206 (2021)
1523-7060
10.1021/acs.orglett.0c03929
1523-7052
1286565061
المصدر المساهم: CSIC
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رقم الانضمام: edsoai.on1286565061
قاعدة البيانات: OAIster