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Journal ArticleDOI

A new method for the preparation of tertiary butyl ethers and esters

Alan Armstrong, +3 more
- 01 Jan 1988 - 
- Vol. 29, Iss: 20, pp 2483-2486
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TLDR
T-butyl 2,2,2-trichloroacetimidate is an efficient reagent for the preparation of t- butyl ethers and esters in the presence of a catalytic amount of boron trifluoride etherate.
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This article is published in Tetrahedron Letters.The article was published on 1988-01-01. It has received 152 citations till now. The article focuses on the topics: Trichloroacetonitrile & Boron trifluoride.

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Citations
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A General Strategy for the Synthesis of Large Peptides: r1~he Combined Solid-Phase and Solution Approach.

TL;DR: The Naα-Fmoc(9-fluorenylmethoxycarbonyl) method allows the selective acidolytic cleavage of fully protected peptides with a free α-carboxyl group from the solid-phase resin to give products in high yield and purity.
Journal ArticleDOI

Design, Synthesis, and Proposed Active Site Binding Analysis of Monocyclic 2-Azetidinone Inhibitors of Prostate Specific Antigen

TL;DR: It is concluded that the design approach has been successful in developing PSA inhibitors and could also be applied to the inhibition of other enzymes, especially in the absence of crystallographic information.
Journal ArticleDOI

Total synthesis of 3-deoxy-D-manno-2-octulosonic acid (KDO) and 2-deoxy-beta-KDO.

TL;DR: In this article, total synthesisation of KDO and 2-deoxy-β-KDO is reported, and the C2-symmetric dienediol was desymmetrized by conversion to its corresponding 1,4-dioxanone.
Journal ArticleDOI

Stereospecific synthesis of dealanylalahopcin

TL;DR: In this article, the first α-amino acid dealanylalahopcin starting from (L) -aspartic acid was described, and the first synthesis of the novel α-AMINO acid was performed starting from
Journal ArticleDOI

9‐Fluorenylmethyloxycarbonyl/ tbutyl‐based convergent protein synthesis

TL;DR: This review summarizes CPS performed utilizing the mild 9-fluorenylmethyloxycarbonyl/tbutyloxy carbonyl-based protecting scheme for the amino acids.
References
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Journal ArticleDOI

New Methods for the Synthesis of Glycosides and Oligosaccharides—Are There Alternatives to the Koenigs‐Knorr Method? [New Synthetic Methods (56)]

TL;DR: Emphasis is placed on glycoside and saccharide formation by 1-O-alkylation, on the trichloroacetimidate method, and on activation through the formation of glycosylsulfonium salts and Glycosyl fluorides.
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Imidoester, I. Darstellung von Trichloracetimidsäureestern

TL;DR: In this article, trichloracetonitril lagert leicht Alkohole unter Bildung von Trichloracetimidsaureestern an: die Reaktion wird durch Alkali (Alkoholat, Salze der Alkoxysauren, Carbonat) katalysiert.
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Darstellung von Carbonsäureestern mittels O‐Alkyl‐N.N′‐dicyclohexyl‐isoharnstoffen

TL;DR: O-Alkyl-N.N′-dicyclohexyl-isoharnstoffe reagieren mit carbonsauren zu Carbonsaureestern.
Journal ArticleDOI

Imidoester, V. Die Umlagerung von Trichloracetimidaten zu N‐substituierten Säureamiden

TL;DR: In this paper, the durch Bortrifluorid katalysierte Umlagerung von Alkyl-trichloracetimidaten (I, R = CCl3, R′ = Alkyls, R″ = H) zu N-substituierten Saureamiden verlauft uber einen ionischen Mechanismus.
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Convenient one-pot esterification of N-protected aminoacids via isopropenyl chloroformate activation.

TL;DR: In this paper, N-protected aminoacids by isopropenyl chloroformate leads to esters of primary, secondary and tertiary alcohols with 4-dimethylamino-pyridine as catalyst.
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