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

32 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 - 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",

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

language = "English (US)",

volume = "24",

pages = "261--264",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd",

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T1 - A stereoselective total synthesis of epi-lupinine

AU - Bremmer, Martin L.

AU - Weinreb, Steven M.

PY - 1983

Y1 - 1983

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).

AB - 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).

UR - https://www.scopus.com/pages/publications/0009579311

UR - https://www.scopus.com/pages/publications/0009579311#tab=citedBy

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

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

M3 - Article

AN - SCOPUS:0009579311

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

All Science Journal Classification (ASJC) codes

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