A stereoselective total synthesis of epi-lupinine

Martin L. Bremmer; Steven M. Weinreb

doi:10.1016/S0040-4039(00)81380-5

A stereoselective total synthesis of epi-lupinine

Martin L. Bremmer, Steven M. Weinreb

Chemistry

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

2 Scopus citations

Abstract

An intromallecular imino Diels-Alder reaction has been used both to construct the quinolizidine ring system and to set the proper relative stereochemistry of the alkaloid epi-lupinine (1).

Original language	English (US)
Pages (from-to)	261-264
Number of pages	4
Journal	Tetrahedron Letters
Volume	24
Issue number	3
DOIs	https://doi.org/10.1016/S0040-4039(00)81380-5
State	Published - Jan 1 1983

All Science Journal Classification (ASJC) codes

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(00)81380-5

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title = "A stereoselective total synthesis of epi-lupinine",

abstract = "An intromallecular imino Diels-Alder reaction has been used both to construct the quinolizidine ring system and to set the proper relative stereochemistry of the alkaloid epi-lupinine (1).",

author = "Bremmer, {Martin L.} and Weinreb, {Steven M.}",

year = "1983",

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doi = "10.1016/S0040-4039(00)81380-5",

language = "English (US)",

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pages = "261--264",

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AU - Bremmer, Martin L.

AU - Weinreb, Steven M.

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N2 - An intromallecular imino Diels-Alder reaction has been used both to construct the quinolizidine ring system and to set the proper relative stereochemistry of the alkaloid epi-lupinine (1).

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U2 - 10.1016/S0040-4039(00)81380-5

DO - 10.1016/S0040-4039(00)81380-5

M3 - Article

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SN - 0040-4039

VL - 24

SP - 261

EP - 264

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 3

ER -

A stereoselective total synthesis of epi-lupinine

Abstract

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