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Use of a sulfinyl tether to control diastereofacial selectivity in [5C + 2C] pyrone-alkene cycloadditions

✍ Scribed by Antonio Rumbo; Luis Castedo; JoséL. Mascareñas

Book ID
104257663
Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
130 KB
Volume
38
Category
Article
ISSN
0040-4039

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📜 SIMILAR VOLUMES

ChemInform Abstract: Use of a Sulfinyl T
ChemInform Abstract: Use of a Sulfinyl Tether to Control Diastereofacial Selectivity in (5C + 2C) Pyrone-Alkene Cycloadditions.
✍ A. RUMBO; L. CASTEDO; J. L. MASCARENAS 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

Use of a Sulfinyl Tether to Control Diastereofacial Selectivity in (5C + 2C) Pyrone-Alkene Cycloadditions. -The incorporation of a sulfoxide group on the tether connecting an alkene to a 4-pyrone diminishes significantly the temperature needed for inducing their thermal (5C + 2C) cycloaddition comp

ChemInform Abstract: Reversal of Stereos
ChemInform Abstract: Reversal of Stereoselectivity in [5 + 2] Pyrone—Alkene Cycloadditions Using a Sulfoxide-to-Sulfoximine Switch. Enantiodivergent Synthesis of 8-Oxabicyclo[3.2.1]octane Systems.
✍ Fernando Lopez; Luis Castedo; Jose L. Mascarenas 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

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