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Highly Diastereoselective and Enantioselective C-H Functionalization of 1,2-Dihydronaphthalenes: A Combined C-H Activation/Cope Rearrangement Followed by a Retro-Cope Rearrangement

ChemInform, 2004-12, Vol.35 (49), p.no-no

2004

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Double C-H Activation Strategy for the Asymmetric Synthesis of C2-Symmetric Anilines

ChemInform, 2004-10, Vol.35 (41), p.no-no

2004

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Double C—H Activation Strategy for the Asymmetric Synthesis of C 2 ‐Symmetric Anilines

ChemInform, 2004-10, Vol.35 (41)

2004

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Intermolecular C-H Activation at Benzylic Positions: Synthesis of (+)-Imperanene and (-)-α-Conidendrin

ChemInform, 2003-07, Vol.34 (30), p.no-no

2003

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ChemInform Abstract: Catalytic Asymmetric Allylic C-H Activation as a Surrogate of the Asymmetric Claisen Rearrangement

ChemInform, 2002-03, Vol.33 (11), p.no-no

2002

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New Strategic Reactions for Organic Synthesis: Catalytic Asymmetric C-H Activation α to Oxygen as a Surrogate to the Aldol Reaction

ChemInform, 2003-12, Vol.34 (49), p.no-no

2003

Volltextzugriff (PDF)

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Highly Diastereoselective and Enantioselective C-H Functionalization of 1,2-Dihydronaphthalenes: A Combined C-H Activation/Cope Rearrangement Followed by a Retro-Cope Rearrangement

Double C-H Activation Strategy for the Asymmetric Synthesis of C2-Symmetric Anilines

Double C—H Activation Strategy for the Asymmetric Synthesis of C 2 ‐Symmetric Anilines

Intermolecular C-H Activation at Benzylic Positions: Synthesis of (+)-Imperanene and (-)-α-Conidendrin

ChemInform Abstract: Catalytic Asymmetric Allylic C-H Activation as a Surrogate of the Asymmetric Claisen Rearrangement

New Strategic Reactions for Organic Synthesis: Catalytic Asymmetric C-H Activation α to Oxygen as a Surrogate to the Aldol Reaction

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