Erratum: Kinetic resolution of activated nitroallylic acetates with aldehydes and ketones through a conjugate addition-elimination SN2' process (European Journal of Organic Chemistry (2012) (353-365))

Raju Jannapu Reddy, Pei Hsun Lee, Dhananjay R. Magar, Jung Hsuan Chen, Kwunmin Chen

Research output: Contribution to journalComment/debate

Abstract

The absolute stereochemistry of the recovered nitroallylic acetates 1 and double bond geometry in the products 3-5 in our original paper were misassigned.[1] The correct chemical structures and stereochemistry for reactions in the presence of either catalyst 2b or 14c are shown in Scheme 1 and Figure 2. Subsequently, corrections of the chemical structure and stereochemistry should be made in the paper accordingly and new Supporting Information is provided. The authors apologize for any inconvenience caused.

Original languageEnglish
Number of pages1
JournalEuropean Journal of Organic Chemistry
Volume2015
Issue number3
DOIs
Publication statusPublished - 2015 Jan

Fingerprint

organic chemistry
Stereochemistry
stereochemistry
Ketones
aldehydes
Aldehydes
ketones
acetates
elimination
Acetates
Kinetics
kinetics
catalysts
Catalysts
Geometry
products
geometry
Organic Chemistry

Keywords

  • Aldehydes
  • Diastereoselectivity
  • Enantioselectivity
  • Ketones
  • Kinetic resolution
  • Organocatalysis

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

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title = "Erratum: Kinetic resolution of activated nitroallylic acetates with aldehydes and ketones through a conjugate addition-elimination SN2' process (European Journal of Organic Chemistry (2012) (353-365))",
abstract = "The absolute stereochemistry of the recovered nitroallylic acetates 1 and double bond geometry in the products 3-5 in our original paper were misassigned.[1] The correct chemical structures and stereochemistry for reactions in the presence of either catalyst 2b or 14c are shown in Scheme 1 and Figure 2. Subsequently, corrections of the chemical structure and stereochemistry should be made in the paper accordingly and new Supporting Information is provided. The authors apologize for any inconvenience caused.",
keywords = "Aldehydes, Diastereoselectivity, Enantioselectivity, Ketones, Kinetic resolution, Organocatalysis",
author = "Reddy, {Raju Jannapu} and Lee, {Pei Hsun} and Magar, {Dhananjay R.} and Chen, {Jung Hsuan} and Kwunmin Chen",
year = "2015",
month = "1",
doi = "10.1002/ejoc.201403513",
language = "English",
volume = "2015",
journal = "Annalen der Pharmacie",
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publisher = "Wiley-VCH Verlag",
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T2 - Kinetic resolution of activated nitroallylic acetates with aldehydes and ketones through a conjugate addition-elimination SN2' process (European Journal of Organic Chemistry (2012) (353-365))

AU - Reddy, Raju Jannapu

AU - Lee, Pei Hsun

AU - Magar, Dhananjay R.

AU - Chen, Jung Hsuan

AU - Chen, Kwunmin

PY - 2015/1

Y1 - 2015/1

N2 - The absolute stereochemistry of the recovered nitroallylic acetates 1 and double bond geometry in the products 3-5 in our original paper were misassigned.[1] The correct chemical structures and stereochemistry for reactions in the presence of either catalyst 2b or 14c are shown in Scheme 1 and Figure 2. Subsequently, corrections of the chemical structure and stereochemistry should be made in the paper accordingly and new Supporting Information is provided. The authors apologize for any inconvenience caused.

AB - The absolute stereochemistry of the recovered nitroallylic acetates 1 and double bond geometry in the products 3-5 in our original paper were misassigned.[1] The correct chemical structures and stereochemistry for reactions in the presence of either catalyst 2b or 14c are shown in Scheme 1 and Figure 2. Subsequently, corrections of the chemical structure and stereochemistry should be made in the paper accordingly and new Supporting Information is provided. The authors apologize for any inconvenience caused.

KW - Aldehydes

KW - Diastereoselectivity

KW - Enantioselectivity

KW - Ketones

KW - Kinetic resolution

KW - Organocatalysis

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U2 - 10.1002/ejoc.201403513

DO - 10.1002/ejoc.201403513

M3 - Comment/debate

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VL - 2015

JO - Annalen der Pharmacie

JF - Annalen der Pharmacie

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IS - 3

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