A novel strategy for the asymmetric synthesis of chiral cyclopropane carboxaldehydes

M Cheeseman; F J P Feuillet; A L Johnson; S D Bull

doi:10.1039/b501847a

A novel strategy for the asymmetric synthesis of chiral cyclopropane carboxaldehydes

M Cheeseman, F J P Feuillet, A L Johnson, S D Bull

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

28 Citations (SciVal)

Abstract

A new way of combining chiral auxiliaries and substrate-directable reactions for asymmetric synthesis is described that employs a three-step sequence of aldol-cyclopropanation-retro-aldol reactions for the stereoselective synthesis of enantiopure cyclopropane carboxaldehydes.

Original language	English
Pages (from-to)	2372-2374
Number of pages	3
Journal	Chemical Communications
Issue number	18
DOIs	https://doi.org/10.1039/b501847a
Publication status	Published - 2005

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ID number: ISI:000228920600019

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10.1039/b501847a

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title = "A novel strategy for the asymmetric synthesis of chiral cyclopropane carboxaldehydes",

abstract = "A new way of combining chiral auxiliaries and substrate-directable reactions for asymmetric synthesis is described that employs a three-step sequence of aldol-cyclopropanation-retro-aldol reactions for the stereoselective synthesis of enantiopure cyclopropane carboxaldehydes.",

author = "M Cheeseman and Feuillet, \{F J P\} and Johnson, \{A L\} and Bull, \{S D\}",

note = "ID number: ISI:000228920600019",

year = "2005",

doi = "10.1039/b501847a",

language = "English",

pages = "2372--2374",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "18",

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T1 - A novel strategy for the asymmetric synthesis of chiral cyclopropane carboxaldehydes

AU - Cheeseman, M

AU - Feuillet, F J P

AU - Johnson, A L

AU - Bull, S D

N1 - ID number: ISI:000228920600019

PY - 2005

Y1 - 2005

N2 - A new way of combining chiral auxiliaries and substrate-directable reactions for asymmetric synthesis is described that employs a three-step sequence of aldol-cyclopropanation-retro-aldol reactions for the stereoselective synthesis of enantiopure cyclopropane carboxaldehydes.

AB - A new way of combining chiral auxiliaries and substrate-directable reactions for asymmetric synthesis is described that employs a three-step sequence of aldol-cyclopropanation-retro-aldol reactions for the stereoselective synthesis of enantiopure cyclopropane carboxaldehydes.

UR - https://www.scopus.com/pages/publications/19944381888

U2 - 10.1039/b501847a

DO - 10.1039/b501847a

M3 - Article

SN - 1359-7345

SP - 2372

EP - 2374

JO - Chemical Communications

JF - Chemical Communications

IS - 18

ER -

A novel strategy for the asymmetric synthesis of chiral cyclopropane carboxaldehydes

Abstract

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