Selective deprotection of trialkylsilyl ethers using fluorosilicic acid

No abstract is available for this paper.

• Publication year

  1992

• Venue

  Journal of Organic Chemistry

• Publication date

  1992-04-01

• Fields of study

  Chemistry

• Identifiers
  DOI 10.1021/JO00034A057
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• No references are available for this paper.

• Regioselective Arene C-H Borylation with a MOF-Immobilized Iridium Bipyridine Catalyst.

  2026cites this paper
• Fluorosilicic acid: secondary raw material and reagent in technological practice and preparative synthesis (a review)

  2023cites this paper
• Total Synthesis of Aflastatin A.

  2022cites this paper
• Synthesis of Polyoxygenated Heterocycles by Diastereoselective Functionalization of a Bio-Based Chiral Aldehyde Exploiting the Passerini Reaction

  2020cites this paper
• Catalytic Activation of Trimethylsilylacetylenes: A One-Pot Route to Unsymmetrical Acetylenes and Heterocycles.

  2018cites this paper
• The First Stereoselective Total Synthesis of (–)‐Synrotolide

  2014cites this paper
• Access to the aeruginosin serine protease inhibitors through the nucleophilic opening of an oxabicyclo[2.2.1]heptane: total synthesis of microcin SF608.

  2014cites this paper
• Journey describing applications of oxone in synthetic chemistry.

  2013cites this paper
• Stereoselective synthesis of highly functionalized thiopeptide thiazole fragments from uronic acid/cysteine condensation products: access to the core dipeptide of the thiazomycins and nocathiacins

  2012cites this paper
• Development for an Improved Process of Selective Prostaglandin Receptor Agonist ONO-4819

  2011cites this paper
• Towards the synthesis of massadine: a unified strategy for the stereoselective synthesis of the carbocyclic C,D-ring subunit.

  2011cites this paper
• Good timing in total synthesis: the case of phoslactomycin A.

  2010cites this paper
• Enantioselective total synthesis of brevetoxin A: convergent coupling strategy and completion.

  2009cites this paper
• Deprotection of a silyl group with mesoporous silica.

  2007cites this paper
• Alkyl‐ and Arylation of Oxacyclic Ethers with Triethylsilyl Triflate — 2,4,6‐Collidine — Gilman Reagent Combination: Remarkable Discrimination of Two Ether Oxygens.

  2007cites this paper
• Reaction of Tetrahydropyranyl Ethers with Triethylsilyl Trifluoromethanesulfonate–2,4,6‐Collidine Combination: Speculation on the Intermediate, Efficient Deprotection, and Application to Efficient Ring‐Closing Metathesis as a Tether

  2007cites this paper
• Apoptolidin A: total synthesis and partially glycosylated analogues.

  2006cites this paper
• Design, synthesis and biological evaluation of novel, simplified analogues of laulimalide: modification of the side chain.

  2005cites this paper
• Selective Monodeprotection of Bis-Silyl Ethers

  2004cites this paper
• Total synthesis of (+/-)-kalihinol C.

  2004cites this paper
• Synthesis of (−)-xialenon A by enantioselective α-deprotonation-rearrangement of a meso-epoxide

  2003cites this paper
• Protection for the Hydroxyl Group, Including 1,2‐ and 1,3‐Diols

  2002cites this paper
• Efficient and chemoselective cleavage of TBS ethers by a sub-stoichiometric amount of decaborane

  2002cites this paper
• Reactions at Oxygen Atoms

  2001cites this paper
• An efficient synthesis of 3-hetero-13,14-dihydro prostaglandin F1alpha analogues.

  2001cites this paper
• Efficient and Selective Protection of Alcohols and Phenols with Triisopropylsilyl Chloride/Imidazole Using Microwave Irradiation

  2000cites this paper
• Steric Effects of Silyl Groups

  1999cites this paper
• A NOVEL, HIGHLY EFFICIENT AND SELECTIVE DESILYLATING METHOD FOR TRIALKYLSILYL ETHERS

  1998cites this paper
• Substrate specificity of human prolyl-4-hydroxylase.

  1998cites this paper
• A vinylogous urethane approach towards the synthesis of okadaic acid. construction of the C9-C18 Fragment. Part II

  1998cites this paper
• 1:1 and 1:2 complexes of Bu4NF and BF3·Et2O: Unique properties as reagents for cleavage of silyl ethers

  1996cites this paper
• A mild and efficient method for the deprotection of tert-butyldimethylsilyl ethers using iodine in methanol

  1996cites this paper
• Selective cleavage of ethers using silica-alumina gel catalysts prepared by the sol-gel method

  1996cites this paper
• Chromium [II]-mediated reductive cleavage of a tertiary halide bearing three β-alkoxy groups. Synthesis of the north hexacyclic steroid unit of the cephalostatin family

  1995cites this paper
• Selective Deprotection of Diphenylmethylsilylethers of Allylic and Benzylic Alcohols

  1995cites this paper
• A simple and highly chemoselective desilylation of tert-butyldimethylsilyl ethers

  1995cites this paper
• An Efficient and Highly Chemoselective Method to Desilylate Silyl Ethers

  1995cites this paper
• A MILD METHOD FOR THE CLEAVAGE OF SI-C BOND IN OLIGONUCLEOTIDE SYNTHESIS

  1995cites this paper
• Utilization of neutral alumina as a mild reagent for the selective cleavage of primary and secondary silyl ethers

  1994cites this paper
• FACILE DEPROTECTION OF SILYL NUCLEOSIDES WITH POTASSIUM FLUORIDE/18-CROWN-6

  1994cites this paper
• Highly stereoselective synthesis of cis-(2R,3S)-3-hydroxyproline

  1993cites this paper
• Chemoenzymatic preparation of a key intermediate for carbapenem synthesis starting from asymmetrized bis(hydroxymethyl)acetaldehyde (BHYMA

  1993cites this paper
• Selectivity in the catalytic transfer hydrogenolysis of silyl ether protecting groups

  1993cites this paper
• Deprotection of silyl ethers using 2,3-dichloro-5,6-dicyano-p-benzoquinone

  1992cites this paper
• Chapter 9. Synthetic methods

  1992cites this paper
• Selective Deprotection of Trialkylsilyl Ethers Using Fluorosilicic Acid.

  1992cites this paper