a two-step reaction sequence for the synthesis of tetrahydronaphthalenes

2

2005 Hydrogenated naphthalene derivatives Q 1010 A Two-Step Reaction Sequence for the Synthesis of Tetrahydronaphthalenes. — Diels—Alder reaction of a boron-functionalized enyne with substituted alkenes affords dihydroaromatic boronic esters (III) and (XXI). The latter are applied in further Diels—Alder sequences to give highly substituted and functionalized products in acceptable to very good yields. Five new C—C bonds from 4 simple components are formed in this process. — (HILT*, G.; LUEERS, S.; SMOLKO, K. I.; Org. Lett. 7 (2005) 2, 251-253; Fachbereich Chem., Philipps-Univ., D-35043 Marburg, Germany; Eng.) — Steudel 22- 086

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Page 1: A Two-Step Reaction Sequence for the Synthesis of Tetrahydronaphthalenes

2005

Hydrogenated naphthalene derivativesQ 1010 A Two-Step Reaction Sequence for the Synthesis of Tetrahydronaphthalenes. —

Diels—Alder reaction of a boron-functionalized enyne with substituted alkenes affords dihydroaromatic boronic esters (III) and (XXI). The latter are applied in further Diels—Alder sequences to give highly substituted and functionalized products in acceptable to very good yields. Five new C—C bonds from 4 simple components are formed in this process. — (HILT*, G.; LUEERS, S.; SMOLKO, K. I.; Org. Lett. 7 (2005) 2, 251-253; Fachbereich Chem., Philipps-Univ., D-35043 Marburg, Germany; Eng.) — Steudel

22- 086

Page 2: A Two-Step Reaction Sequence for the Synthesis of Tetrahydronaphthalenes

2005

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