Stereochemistry of contiguous cyclopropane formation from cascade cyclization of a skipped dienyl homoallyl triflate

Christopher Lincoln; James D. White; Alexandre F.T. Yokochi

doi:10.1039/b412811g

Stereochemistry of contiguous cyclopropane formation from cascade cyclization of a skipped dienyl homoallyl triflate

Christopher Lincoln, James D. White, Alexandre F.T. Yokochi

Houston Methodist

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

9 Scopus citations

Abstract

Solvolysis of asymmetric homoallylic triflates bearing a terminal stannyl substituent gives disubstituted cyclopropanes and bicyclopropanes bearing differentiated termini in high enantiopurity.

Original language	English (US)
Pages (from-to)	2846-2847
Number of pages	2
Journal	Chemical Communications
Issue number	24
DOIs	https://doi.org/10.1039/b412811g
State	Published - Dec 21 2004

ASJC Scopus subject areas

Catalysis
Electronic, Optical and Magnetic Materials
Ceramics and Composites
General Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Materials Chemistry

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title = "Stereochemistry of contiguous cyclopropane formation from cascade cyclization of a skipped dienyl homoallyl triflate",

abstract = "Solvolysis of asymmetric homoallylic triflates bearing a terminal stannyl substituent gives disubstituted cyclopropanes and bicyclopropanes bearing differentiated termini in high enantiopurity.",

author = "Christopher Lincoln and White, \{James D.\} and Yokochi, \{Alexandre F.T.\}",

year = "2004",

month = dec,

day = "21",

doi = "10.1039/b412811g",

language = "English (US)",

pages = "2846--2847",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

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T1 - Stereochemistry of contiguous cyclopropane formation from cascade cyclization of a skipped dienyl homoallyl triflate

AU - Lincoln, Christopher

AU - White, James D.

AU - Yokochi, Alexandre F.T.

PY - 2004/12/21

Y1 - 2004/12/21

N2 - Solvolysis of asymmetric homoallylic triflates bearing a terminal stannyl substituent gives disubstituted cyclopropanes and bicyclopropanes bearing differentiated termini in high enantiopurity.

AB - Solvolysis of asymmetric homoallylic triflates bearing a terminal stannyl substituent gives disubstituted cyclopropanes and bicyclopropanes bearing differentiated termini in high enantiopurity.

UR - https://www.scopus.com/pages/publications/11244327658

UR - https://www.scopus.com/inward/citedby.url?scp=11244327658&partnerID=8YFLogxK

U2 - 10.1039/b412811g

DO - 10.1039/b412811g

M3 - Article

AN - SCOPUS:11244327658

SN - 1359-7345

SP - 2846

EP - 2847

JO - Chemical Communications

JF - Chemical Communications

IS - 24

ER -

Stereochemistry of contiguous cyclopropane formation from cascade cyclization of a skipped dienyl homoallyl triflate

Abstract

ASJC Scopus subject areas

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