A new general access to either type of securinega alkaloids: Synthesis of securinine and (-)-allonorsecurinine

Ramon Alibés; Marta Ballbé; Félix Busqué; Pedro De March; Laia Elias; Marta Figueredo; Josep Font

doi:10.1021/ol049455+

A new general access to either type of securinega alkaloids: Synthesis of securinine and (-)-allonorsecurinine

Ramon Alibés, Marta Ballbé, Félix Busqué, Pedro De March, Laia Elias, Marta Figueredo, Josep Font

Department of Chemistry

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

48 Citations (Scopus)

Abstract

Matrix presented. The syntheses of securinine and (-)-allonorsecurinine have been achieved starting from easily available α-amino acid derivatives and using as key steps a RCM and a Heck reaction for the formation of rings D and C, respectively.

Original language	English
Pages (from-to)	1813-1816
Journal	Organic Letters
Volume	6
Issue number	11
DOIs	https://doi.org/10.1021/ol049455+
Publication status	Published - 27 May 2004

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@article{33316161221244b59132e71e8e05aa77,

title = "A new general access to either type of securinega alkaloids: Synthesis of securinine and (-)-allonorsecurinine",

abstract = "Matrix presented. The syntheses of securinine and (-)-allonorsecurinine have been achieved starting from easily available α-amino acid derivatives and using as key steps a RCM and a Heck reaction for the formation of rings D and C, respectively.",

author = "Ramon Alib{\'e}s and Marta Ballb{\'e} and F{\'e}lix Busqu{\'e} and {De March}, Pedro and Laia Elias and Marta Figueredo and Josep Font",

year = "2004",

month = may,

day = "27",

doi = "10.1021/ol049455+",

language = "English",

volume = "6",

pages = "1813--1816",

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TY - JOUR

T1 - A new general access to either type of securinega alkaloids: Synthesis of securinine and (-)-allonorsecurinine

AU - Alibés, Ramon

AU - Ballbé, Marta

AU - Busqué, Félix

AU - De March, Pedro

AU - Elias, Laia

AU - Figueredo, Marta

AU - Font, Josep

PY - 2004/5/27

Y1 - 2004/5/27

N2 - Matrix presented. The syntheses of securinine and (-)-allonorsecurinine have been achieved starting from easily available α-amino acid derivatives and using as key steps a RCM and a Heck reaction for the formation of rings D and C, respectively.

AB - Matrix presented. The syntheses of securinine and (-)-allonorsecurinine have been achieved starting from easily available α-amino acid derivatives and using as key steps a RCM and a Heck reaction for the formation of rings D and C, respectively.

U2 - 10.1021/ol049455+

DO - 10.1021/ol049455+

M3 - Article

SN - 1523-7060

VL - 6

SP - 1813

EP - 1816

JO - Organic Letters

JF - Organic Letters

IS - 11

ER -

A new general access to either type of securinega alkaloids: Synthesis of securinine and (-)-allonorsecurinine

Abstract

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