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Recent developments in the area of anndlated furans. a review

Albert Padwa, +1 more
- 01 Aug 1991 - 
- Vol. 23, Iss: 4, pp 545-568
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This article is published in Organic Preparations and Procedures International.The article was published on 1991-08-01. It has received 13 citations till now.

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Citations
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Electrochemical strategies for C-H functionalization and C-N bond formation.

TL;DR: This review provides an overview on the use of anodic electrochemical methods for expediting the development of carbon-hydrogen functionalization and carbon-nitrogen bond formation strategies and aims to provide inspiration for future synthetic applications in the field of electrosynthesis.
Journal ArticleDOI

Studies on the sequential multi-component coupling/Diels–Alder cycloaddition reaction

TL;DR: In this paper, the synthesis of highly functionalized oxabicyclo[2.2.1]heptadiene derivatives through the sequential use of an Ugi or Passerini multi-component coupling reaction followed by an intramolecular acetylene/furan Diels-Alder reaction was investigated.
Journal ArticleDOI

Electrooxidative coupling of furans and silyl enol ethers: application to the synthesis of annulated furans.

TL;DR: The preparation of annulated furan systems as key synthetic intermediates through the application of a two-step annulation involving an electrochemical ring closure between a furan and a silyl enol ether has been studied.
Journal ArticleDOI

A regioselective addition reaction of a sulfonyl radical to conjugate enynesulfones: A convenient synthesis of 1,4-bis(arylsulfonyl)-1,3-butadiene

TL;DR: Tolyl benzeneselenosulfonate regioselectively added to the conjugate enynesulfones 1−9 gave (1 E,3 E )-1,4-bis(arylsulfonyl)-1,3-butadienes 10−17, which were converted to the 4-hetero atom-substituted-1-phenylsulfonyls- 1,3butadiens 18, 21 and 22 as mentioned in this paper.
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Tungsten η1-Five-Membered Oxygenated Heterocycles Derived from Tungsten η1-Propargyl Compounds: Systematic Syntheses, Structural Rearrangement, Electrophilic Alkylations, and Oxidative Demetalations

TL;DR: In the presence of BF3·Et2O, Tungsten η1-propargyl complexes reacted smoothly with aldehydes to give tungsten 1-2,5-dihydro-3-furyl complexes 1−3 as discussed by the authors.
References
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Book

Comprehensive Heterocyclic Chemistry II

TL;DR: In this article, the CHEC III is organized in 15 volumes and closely follows the organization used in the previous edition: Volumes 1 and 2: Cover respectively three and four-membered heterocycles, together with all fused systems containing a three- or four-measured heterocyclic ring.
Journal ArticleDOI

Preparation, metallation and alkylation of allenyl ethers

TL;DR: Propargyl ethers HCCCH2OR [R = alkyl or-CH(CH8)(OC2H5)] have been isomerized with good yields into the corresponding allenyl ether's CH2CCHOR by warming with potassium tert-butoxide at 70°.
Book

The Total Synthesis of Natural Products

John ApSimon
TL;DR: The Total Synthesis of Macrocyclic Lactones Synthesis for the Leukotrienes Synthesis as discussed by the authors, 1980 - 1986, is a classic work in the field of macrocyclic lactones.