A short and efficient synthesis of (R)-(-)-sporochnol A

Ramón Alibés; Félix Busqué; Gisela G. Bardají; Pedro de March; Marta Figueredo; Josep Font

doi:10.1016/j.tetasy.2006.09.013

A short and efficient synthesis of (R)-(-)-sporochnol A

Ramón Alibés, Félix Busqué, Gisela G. Bardají, Pedro de March, Marta Figueredo, Josep Font

Department of Chemistry

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

7 Citations (Scopus)

Abstract

A short and efficient synthesis of (R)-(-)-sporochnol A in five steps and 9% overall yield has been developed. The sequence uses as starting material the easily available enantiopure monoketal derived from 1,4-cyclohexanedione and (R,R)-hydrobenzoin that serves as a chiral auxiliary. © 2006 Elsevier Ltd. All rights reserved.

Original language	English
Pages (from-to)	2632-2636
Journal	Tetrahedron Asymmetry
Volume	17
Issue number	18
DOIs	https://doi.org/10.1016/j.tetasy.2006.09.013
Publication status	Published - 16 Oct 2006

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title = "A short and efficient synthesis of (R)-(-)-sporochnol A",

abstract = "A short and efficient synthesis of (R)-(-)-sporochnol A in five steps and 9% overall yield has been developed. The sequence uses as starting material the easily available enantiopure monoketal derived from 1,4-cyclohexanedione and (R,R)-hydrobenzoin that serves as a chiral auxiliary. {\textcopyright} 2006 Elsevier Ltd. All rights reserved.",

author = "Ram{\'o}n Alib{\'e}s and F{\'e}lix Busqu{\'e} and Bardaj{\'i}, {Gisela G.} and {de March}, Pedro and Marta Figueredo and Josep Font",

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T1 - A short and efficient synthesis of (R)-(-)-sporochnol A

AU - Alibés, Ramón

AU - Busqué, Félix

AU - Bardají, Gisela G.

AU - de March, Pedro

AU - Figueredo, Marta

AU - Font, Josep

PY - 2006/10/16

Y1 - 2006/10/16

N2 - A short and efficient synthesis of (R)-(-)-sporochnol A in five steps and 9% overall yield has been developed. The sequence uses as starting material the easily available enantiopure monoketal derived from 1,4-cyclohexanedione and (R,R)-hydrobenzoin that serves as a chiral auxiliary. © 2006 Elsevier Ltd. All rights reserved.

AB - A short and efficient synthesis of (R)-(-)-sporochnol A in five steps and 9% overall yield has been developed. The sequence uses as starting material the easily available enantiopure monoketal derived from 1,4-cyclohexanedione and (R,R)-hydrobenzoin that serves as a chiral auxiliary. © 2006 Elsevier Ltd. All rights reserved.

U2 - 10.1016/j.tetasy.2006.09.013

DO - 10.1016/j.tetasy.2006.09.013

M3 - Article

VL - 17

SP - 2632

EP - 2636

IS - 18

ER -