Facile Lewis Acid-Mediated Ring Opening of 4-Hydroxypyrrolidin-2-ones by Amino Acid Esters

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7 Citations (Scopus)

Abstract

Lewis acid mediated ring opening of 4-hydroxypyrrolidin-2-ones by certain amino acid t-butyl esters leads directly to hydroxyethylene dipeptides.

Original languageEnglish
Pages (from-to)479-480
Number of pages2
JournalSynlett
Volume1996
Issue number5
DOIs
StatePublished - 1 Jan 1996

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Lewis Acids
Dipeptides
Esters
Amino Acids
hydroxyethylene

Cite this

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title = "Facile Lewis Acid-Mediated Ring Opening of 4-Hydroxypyrrolidin-2-ones by Amino Acid Esters",
abstract = "Lewis acid mediated ring opening of 4-hydroxypyrrolidin-2-ones by certain amino acid t-butyl esters leads directly to hydroxyethylene dipeptides.",
author = "David Rotella",
year = "1996",
month = "1",
day = "1",
doi = "10.1055/s-1996-5456",
language = "English",
volume = "1996",
pages = "479--480",
journal = "Synlett",
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}

Facile Lewis Acid-Mediated Ring Opening of 4-Hydroxypyrrolidin-2-ones by Amino Acid Esters. / Rotella, David.

In: Synlett, Vol. 1996, No. 5, 01.01.1996, p. 479-480.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

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AU - Rotella, David

PY - 1996/1/1

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N2 - Lewis acid mediated ring opening of 4-hydroxypyrrolidin-2-ones by certain amino acid t-butyl esters leads directly to hydroxyethylene dipeptides.

AB - Lewis acid mediated ring opening of 4-hydroxypyrrolidin-2-ones by certain amino acid t-butyl esters leads directly to hydroxyethylene dipeptides.

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U2 - 10.1055/s-1996-5456

DO - 10.1055/s-1996-5456

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VL - 1996

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EP - 480

JO - Synlett

JF - Synlett

SN - 0936-5214

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