Search

Now showing items 1-10 of 14

Procedures for and Possible Mechanisms of Pd-Catalyzed Allylations of Primary and Secondary Amines with Allylic Alcohols

Type: Journal Paper

Author : Jacques Muzart

Year: 2007

Request PDF

Palladium-catalysed reactions of alcohols. Part B: Formation of C–C and C–N bonds from unsaturated alcohols

Type: Journal Paper

Author : Jacques Muzart

Year: 2005

Request PDF

Palladium-catalysed oxidation of primary and secondary alcohols

Type: Journal Paper

Author : Jacques Muzart

Publisher: Elsevier Science

Year: 2003

Request PDF

Palladium-catalysed reactions of alcohols. Part D: Rearrangements, carbonylations, carboxylations and miscellaneous reactions

Type: Journal Paper

Author : Jacques Muzart

Year: 2005

Request PDF

Silyl Ethers as Protective Groups for Alcohols: Oxidative Deprotection and Stability under Alcohol Oxidation Conditions

Type: Journal Paper

Author : Jacques Muzart

Year: 1993

Request PDF

Production of Csp3-Csp3Bonds through Palladium-Catalyzed Tsuji-Trost-Type Reactions of (Hetero)Benzylic Substrates

Type: Journal Paper

Author : Jean Le Bras; Jacques Muzart

Year: 2016

Request PDF

Selective copper-catalyzed allylic oxidations using a 1/1 ratio of cycloalkene and tert-butylperbenzoate

Type: Journal Paper

Author : Jean Le Bras; Jacques Muzart

Publisher: Elsevier Science

Year: 2002

Request PDF

Pd-catalyzed reduction of aryl halides using dimethylformamide as the hydride source

Type: Journal Paper

Author : Anna Maria Zawisza; Jacques Muzart

Year: 2007

Request PDF

Chromium-exchanged zeolite (CrE-ZSM-5) as catalyst for alcohol oxidation and benzylic oxidation with t-BuOOH

Type: Journal Paper

Author : Zoubida Lounis; Abdelkhalek Riahi; Fatiha Djafri; Jacques Muzart

Year: 2006

Request PDF

Water-mediated transition-metal-free Tsuji–Trost-type reaction

Type: Journal Paper

Author : Carole Chevrin; Jean Le Bras; Françoise Hénin; Jacques Muzart

Year: 2003

Request PDF

Search

Procedures for and Possible Mechanisms of Pd-Catalyzed Allylations of Primary and Secondary Amines with Allylic Alcohols

Palladium-catalysed reactions of alcohols. Part B: Formation of C–C and C–N bonds from unsaturated alcohols

Palladium-catalysed oxidation of primary and secondary alcohols

Palladium-catalysed reactions of alcohols. Part D: Rearrangements, carbonylations, carboxylations and miscellaneous reactions

Silyl Ethers as Protective Groups for Alcohols: Oxidative Deprotection and Stability under Alcohol Oxidation Conditions

Production of Csp3-Csp3Bonds through Palladium-Catalyzed Tsuji-Trost-Type Reactions of (Hetero)Benzylic Substrates

Selective copper-catalyzed allylic oxidations using a 1/1 ratio of cycloalkene and tert-butylperbenzoate

Pd-catalyzed reduction of aryl halides using dimethylformamide as the hydride source

Chromium-exchanged zeolite (CrE-ZSM-5) as catalyst for alcohol oxidation and benzylic oxidation with t-BuOOH

Water-mediated transition-metal-free Tsuji–Trost-type reaction

Author

Publisher

Year

Type

Language (ISO)

Content Type

Publication Title

Search

Filters

Procedures for and Possible Mechanisms of Pd-Catalyzed Allylations of Primary and Secondary Amines with Allylic Alcohols

Palladium-catalysed reactions of alcohols. Part B: Formation of C–C and C–N bonds from unsaturated alcohols

Palladium-catalysed oxidation of primary and secondary alcohols

Palladium-catalysed reactions of alcohols. Part D: Rearrangements, carbonylations, carboxylations and miscellaneous reactions

Silyl Ethers as Protective Groups for Alcohols: Oxidative Deprotection and Stability under Alcohol Oxidation Conditions

Production of Csp3-Csp3Bonds through Palladium-Catalyzed Tsuji-Trost-Type Reactions of (Hetero)Benzylic Substrates

Selective copper-catalyzed allylic oxidations using a 1/1 ratio of cycloalkene and tert-butylperbenzoate

Pd-catalyzed reduction of aryl halides using dimethylformamide as the hydride source

Chromium-exchanged zeolite (CrE-ZSM-5) as catalyst for alcohol oxidation and benzylic oxidation with t-BuOOH

Water-mediated transition-metal-free Tsuji–Trost-type reaction