Tandem and domino catalytic strategies for enantioselective synthesis

C.J. Chapman, C.G. Frost

Research output: Contribution to journalArticle

399 Citations (Scopus)

Abstract

Catalytic asymmetric methodologies provide versatile routes to many complex molecules through expedient and often elegant processes. This review summarises the work on the development and application of tandem and domino catalysed reactions within enantioselective organic synthesis. 1 Introduction 2 Transition-Metal-Catalysed Processes 2.1 Processes Involving Michael Additions 2.2 Hydroformylations 2.3 Heck Reactions 2.4 Allylic Substitutions 2.5 Processes Involving Pericyclic Reactions 2.6 Hydrogenations 2.7 Aldol Reactions 2.8 Metathesis Reactions 2.9 Processes Involving Epoxide Formation 2.10 Miscellaneous Transition-Metal-Catalysed Processes 3 Chiral Organocatalytic Reactions 3.1 Processes Involving Michael Additions 3.2 Aldol Reactions 3.3 Mannich Reactions 3.4 Processes Involving Pericyclic Reactions 3.5 Miscellaneous Organocatalytic Processes 4 Conclusions.
Original languageEnglish
Pages (from-to)1-21
Number of pages21
JournalSynthesis
Volume2007
Issue number1
DOIs
Publication statusPublished - 4 Jan 2007

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Transition metals
Hydroformylation
Epoxy Compounds
Hydrogenation
Substitution reactions
Molecules
3-hydroxybutanal

Cite this

Tandem and domino catalytic strategies for enantioselective synthesis. / Chapman, C.J.; Frost, C.G.

In: Synthesis, Vol. 2007, No. 1, 04.01.2007, p. 1-21.

Research output: Contribution to journalArticle

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