Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (±)-hippodamine and (±)-epi-hippodamine

Martin Rejzek; Robert A. Stockman; David L. Hughes

doi:10.1039/b413052a

Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (±)-hippodamine and (±)-epi-hippodamine

Martin Rejzek, Robert A. Stockman, David L. Hughes

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

30 Citations (Scopus)

Abstract

Two-directional total stereoselective syntheses of (±)-hippodamine and (±)-epi-hippodamine, utilising a tandem deprotection/intramolecular double Michael addition sequence as the key step, are presented.

Original language	English
Pages (from-to)	73-83
Number of pages	11
Journal	Organic & Biomolecular Chemistry
Volume	3
Issue number	1
DOIs	https://doi.org/10.1039/b413052a
Publication status	Published - 1 Jan 2005

Access to Document

10.1039/b413052a

Cite this

@article{dbb0bd9bd4a147e9b4f7fa46276df444,

title = "Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (±)-hippodamine and (±)-epi-hippodamine",

abstract = "Two-directional total stereoselective syntheses of (±)-hippodamine and (±)-epi-hippodamine, utilising a tandem deprotection/intramolecular double Michael addition sequence as the key step, are presented.",

author = "Martin Rejzek and Stockman, {Robert A.} and Hughes, {David L.}",

year = "2005",

month = jan,

day = "1",

doi = "10.1039/b413052a",

language = "English",

volume = "3",

pages = "73--83",

journal = "Organic & Biomolecular Chemistry",

issn = "1477-0520",

publisher = "Royal Society of Chemistry",

number = "1",

}

TY - JOUR

T1 - Combining two-directional synthesis and tandem reactions: an efficient strategy for the total syntheses of (±)-hippodamine and (±)-epi-hippodamine

AU - Rejzek, Martin

AU - Stockman, Robert A.

AU - Hughes, David L.

PY - 2005/1/1

Y1 - 2005/1/1

N2 - Two-directional total stereoselective syntheses of (±)-hippodamine and (±)-epi-hippodamine, utilising a tandem deprotection/intramolecular double Michael addition sequence as the key step, are presented.

AB - Two-directional total stereoselective syntheses of (±)-hippodamine and (±)-epi-hippodamine, utilising a tandem deprotection/intramolecular double Michael addition sequence as the key step, are presented.

U2 - 10.1039/b413052a

DO - 10.1039/b413052a

M3 - Article

VL - 3

SP - 73

EP - 83

JO - Organic & Biomolecular Chemistry

JF - Organic & Biomolecular Chemistry

SN - 1477-0520

IS - 1

ER -