Effects of allylic and homoallylic substituents on the ring closing metathesis reaction used to synthesise simplified eleuthesides

Lorenzo Caggiano; Damiano Castoldi; Raphael Beumer; Pau Bayón; Joachim Telser; Cesare Gennari

doi:10.1016/j.tetlet.2003.09.010

Effects of allylic and homoallylic substituents on the ring closing metathesis reaction used to synthesise simplified eleuthesides

Lorenzo Caggiano, Damiano Castoldi, Raphael Beumer, Pau Bayón, Joachim Telser, Cesare Gennari

Department of Chemistry

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

45 Citations (Scopus)

Abstract

During the course of our synthetic studies towards simplified eleuthesides, we have found that p-methoxyphenyl (PMP) protected allylic alcohols are compatible with the RCM reaction and can give better yields than the corresponding free allylic alcohols. © 2003 Elsevier Ltd. All rights reserved.

Original language	English
Pages (from-to)	7913-7919
Journal	Tetrahedron Letters
Volume	44
Issue number	43
DOIs	https://doi.org/10.1016/j.tetlet.2003.09.010
Publication status	Published - 20 Oct 2003

Keywords

Antitumour compounds
P-methoxyphenyl (PMP)
Protective groups
Ring closing metathesis

Access to Document

10.1016/j.tetlet.2003.09.010

Cite this

@article{4cdf6c5e30944538883ea51ac9f08f7d,

title = "Effects of allylic and homoallylic substituents on the ring closing metathesis reaction used to synthesise simplified eleuthesides",

abstract = "During the course of our synthetic studies towards simplified eleuthesides, we have found that p-methoxyphenyl (PMP) protected allylic alcohols are compatible with the RCM reaction and can give better yields than the corresponding free allylic alcohols. {\textcopyright} 2003 Elsevier Ltd. All rights reserved.",

keywords = "Antitumour compounds, P-methoxyphenyl (PMP), Protective groups, Ring closing metathesis",

author = "Lorenzo Caggiano and Damiano Castoldi and Raphael Beumer and Pau Bay{\'o}n and Joachim Telser and Cesare Gennari",

year = "2003",

month = oct,

day = "20",

doi = "10.1016/j.tetlet.2003.09.010",

language = "English",

volume = "44",

pages = "7913--7919",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "43",

}

TY - JOUR

T1 - Effects of allylic and homoallylic substituents on the ring closing metathesis reaction used to synthesise simplified eleuthesides

AU - Caggiano, Lorenzo

AU - Castoldi, Damiano

AU - Beumer, Raphael

AU - Bayón, Pau

AU - Telser, Joachim

AU - Gennari, Cesare

PY - 2003/10/20

Y1 - 2003/10/20

N2 - During the course of our synthetic studies towards simplified eleuthesides, we have found that p-methoxyphenyl (PMP) protected allylic alcohols are compatible with the RCM reaction and can give better yields than the corresponding free allylic alcohols. © 2003 Elsevier Ltd. All rights reserved.

AB - During the course of our synthetic studies towards simplified eleuthesides, we have found that p-methoxyphenyl (PMP) protected allylic alcohols are compatible with the RCM reaction and can give better yields than the corresponding free allylic alcohols. © 2003 Elsevier Ltd. All rights reserved.

KW - Antitumour compounds

KW - P-methoxyphenyl (PMP)

KW - Protective groups

KW - Ring closing metathesis

U2 - 10.1016/j.tetlet.2003.09.010

DO - 10.1016/j.tetlet.2003.09.010

M3 - Article

SN - 0040-4039

VL - 44

SP - 7913

EP - 7919

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 43

ER -

Effects of allylic and homoallylic substituents on the ring closing metathesis reaction used to synthesise simplified eleuthesides

Abstract

Keywords

Access to Document

Fingerprint

Cite this