Studies directed toward the total synthesis of the rubradirin antibiotics. 4. A new Diels-Alder-Claisen effective diene

Alan P. Kozikowski; Kiyoshi Sugiyama; Edward Huie

doi:10.1016/S0040-4039(01)81911-0

Studies directed toward the total synthesis of the rubradirin antibiotics. 4. A new Diels-Alder-Claisen effective diene

Alan P. Kozikowski, Kiyoshi Sugiyama, Edward Huie

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

10 Scopus citations

Abstract

A new diene has been synthesized which effectively couples the Diels-Alder reaction with the Claisen rearrangement.

Original language	English (US)
Pages (from-to)	3381-3384
Number of pages	4
Journal	Tetrahedron Letters
Volume	22
Issue number	35
DOIs	https://doi.org/10.1016/S0040-4039(01)81911-0
State	Published - 1981
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(01)81911-0

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@article{f520ee2f06a742049b0d404810410678,

title = "Studies directed toward the total synthesis of the rubradirin antibiotics. 4. A new Diels-Alder-Claisen effective diene",

abstract = "A new diene has been synthesized which effectively couples the Diels-Alder reaction with the Claisen rearrangement.",

author = "Kozikowski, {Alan P.} and Kiyoshi Sugiyama and Edward Huie",

note = "Funding Information: This work was supported by Merck Sharp & Dohmea nd by the Sloan Foundation.",

year = "1981",

doi = "10.1016/S0040-4039(01)81911-0",

language = "English (US)",

volume = "22",

pages = "3381--3384",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "35",

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T1 - Studies directed toward the total synthesis of the rubradirin antibiotics. 4. A new Diels-Alder-Claisen effective diene

AU - Kozikowski, Alan P.

AU - Sugiyama, Kiyoshi

AU - Huie, Edward

N1 - Funding Information: This work was supported by Merck Sharp & Dohmea nd by the Sloan Foundation.

PY - 1981

Y1 - 1981

N2 - A new diene has been synthesized which effectively couples the Diels-Alder reaction with the Claisen rearrangement.

AB - A new diene has been synthesized which effectively couples the Diels-Alder reaction with the Claisen rearrangement.

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U2 - 10.1016/S0040-4039(01)81911-0

DO - 10.1016/S0040-4039(01)81911-0

M3 - Article

AN - SCOPUS:0019410771

SN - 0040-4039

VL - 22

SP - 3381

EP - 3384

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 35

ER -

Studies directed toward the total synthesis of the rubradirin antibiotics. 4. A new Diels-Alder-Claisen effective diene

Abstract

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