2.15 Selected Diastereoselective Reactions

Substrate Controlled Stereoselective Conjugate Addition Reactions with Organocopper Reagents

P. Siengalewicz, J. Mulzer, U. Rinner

Research output: Chapter in Book/Report/Conference proceedingChapter

3 Citations (Scopus)

Abstract

The importance of conjugate addition reactions with organocopper reagents has increased since the seminal synthetic application, as reported by Robinson in the early 1940s. This review chapter is intended to provide an overview of substrate-controlled diastereoselective conjugate organocuprate addition reactions, utilized in the preparation of complex natural products on selected syntheses which have been published within the past decade.

Original languageEnglish
Title of host publicationComprehensive Chirality
PublisherElsevier Ltd
Pages441-471
Number of pages31
Volume2
ISBN (Print)9780080951683
DOIs
Publication statusPublished - Sep 2012

Fingerprint

Addition reactions
Substrates
Biological Products

Keywords

  • Complex natural products
  • Diastereoselective conjugate organocuprate addition reactions
  • Organocopper reagents

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

2.15 Selected Diastereoselective Reactions : Substrate Controlled Stereoselective Conjugate Addition Reactions with Organocopper Reagents. / Siengalewicz, P.; Mulzer, J.; Rinner, U.

Comprehensive Chirality. Vol. 2 Elsevier Ltd, 2012. p. 441-471.

Research output: Chapter in Book/Report/Conference proceedingChapter

@inbook{2c2e9b95fc96450d84ffd2976519b3ba,
title = "2.15 Selected Diastereoselective Reactions: Substrate Controlled Stereoselective Conjugate Addition Reactions with Organocopper Reagents",
abstract = "The importance of conjugate addition reactions with organocopper reagents has increased since the seminal synthetic application, as reported by Robinson in the early 1940s. This review chapter is intended to provide an overview of substrate-controlled diastereoselective conjugate organocuprate addition reactions, utilized in the preparation of complex natural products on selected syntheses which have been published within the past decade.",
keywords = "Complex natural products, Diastereoselective conjugate organocuprate addition reactions, Organocopper reagents",
author = "P. Siengalewicz and J. Mulzer and U. Rinner",
year = "2012",
month = "9",
doi = "10.1016/B978-0-08-095167-6.00225-1",
language = "English",
isbn = "9780080951683",
volume = "2",
pages = "441--471",
booktitle = "Comprehensive Chirality",
publisher = "Elsevier Ltd",

}

TY - CHAP

T1 - 2.15 Selected Diastereoselective Reactions

T2 - Substrate Controlled Stereoselective Conjugate Addition Reactions with Organocopper Reagents

AU - Siengalewicz, P.

AU - Mulzer, J.

AU - Rinner, U.

PY - 2012/9

Y1 - 2012/9

N2 - The importance of conjugate addition reactions with organocopper reagents has increased since the seminal synthetic application, as reported by Robinson in the early 1940s. This review chapter is intended to provide an overview of substrate-controlled diastereoselective conjugate organocuprate addition reactions, utilized in the preparation of complex natural products on selected syntheses which have been published within the past decade.

AB - The importance of conjugate addition reactions with organocopper reagents has increased since the seminal synthetic application, as reported by Robinson in the early 1940s. This review chapter is intended to provide an overview of substrate-controlled diastereoselective conjugate organocuprate addition reactions, utilized in the preparation of complex natural products on selected syntheses which have been published within the past decade.

KW - Complex natural products

KW - Diastereoselective conjugate organocuprate addition reactions

KW - Organocopper reagents

UR - http://www.scopus.com/inward/record.url?scp=84902425239&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84902425239&partnerID=8YFLogxK

U2 - 10.1016/B978-0-08-095167-6.00225-1

DO - 10.1016/B978-0-08-095167-6.00225-1

M3 - Chapter

SN - 9780080951683

VL - 2

SP - 441

EP - 471

BT - Comprehensive Chirality

PB - Elsevier Ltd

ER -