115 related articles for article (PubMed ID: 11430084)
1. The particular sensitivity of silyl ethers of D-glucal toward two Vilsmeier-Haack reagents POCl3.DMF and (CF3SO2)2O.DMF. Their unique and selective conversion to the corresponding C(6)-O-formates.
Lellouche JP; Koeller S
J Org Chem; 2001 Feb; 66(3):693-6. PubMed ID: 11430084
[TBL] [Abstract][Full Text] [Related]
2. A simple homemade reaction station for use in parallel solution-phase synthesis. Optimization of a regioselective one-step deprotective o-formylation reaction mediated by the Vilsmeier-Haack reagent POCl3.DMF.
Kotlyar V; Shahar L; Lellouche JP
Mol Divers; 2006 May; 10(2):255-64. PubMed ID: 16710806
[TBL] [Abstract][Full Text] [Related]
3. A selective Sc(OTf)3-catalyzed trialkylsilyl ether to acetyl ester exchange reaction with beta-l-idopyranoside and 3,4-O-isopropylidene-beta-D-galactopyranoside derivatives.
Ke W; Whitfield DM
Carbohydr Res; 2004 Dec; 339(18):2841-50. PubMed ID: 15582610
[TBL] [Abstract][Full Text] [Related]
4. P(MeNCH2CH2)3N: an efficient catalyst for the desilylation of tert-butyldimethylsilyl ethers.
Yu Z; Verkade JG
J Org Chem; 2000 Apr; 65(7):2065-8. PubMed ID: 10774026
[TBL] [Abstract][Full Text] [Related]
5. O-Silylated C3-halohydrins as a novel class of protected building blocks for total, regio- and stereocontrolled synthesis of glycerolipid frameworks.
Stamatov SD; Stawinski J
Org Biomol Chem; 2010 Jan; 8(2):463-77. PubMed ID: 20066285
[TBL] [Abstract][Full Text] [Related]
6. Vilsmeier-Haack-Initiated Formylative Rearrangement of Spirodioxo-lan-5-ones into Functionalized 4,5,6,7-Tetrahydrobenzofurans.
Varenichenko SA; Markov V; Goebel JF; Gooßen LJ; Farat OK
J Org Chem; 2024 Mar; 89(5):2840-2846. PubMed ID: 38329890
[TBL] [Abstract][Full Text] [Related]
7. Use of XtalFluor-E as an Alternative to POCl
Roudias M; Vallée F; Martel J; Paquin JF
J Org Chem; 2018 Aug; 83(15):8731-8738. PubMed ID: 29989816
[TBL] [Abstract][Full Text] [Related]
8. Influence of Various Silyl Protecting Groups on Stereoselective 2-Deoxyrhamnosylation.
Mukherji A; Rotta MKV; Sarmah BK; Kancharla PK
J Org Chem; 2023 Jan; 88(1):245-260. PubMed ID: 36524596
[TBL] [Abstract][Full Text] [Related]
9. Chemoselective deprotection of triethylsilyl ethers.
Chandra T; Broderick WE; Broderick JB
Nucleosides Nucleotides Nucleic Acids; 2009 Nov; 28(11):1016-29. PubMed ID: 20183570
[TBL] [Abstract][Full Text] [Related]
10. Facile cleavage of triethylsilyl (TES) ethers using o-iodoxybenzoic acid (IBX) without affecting tert-butyldimethylsilyl (TBS) ethers.
Wu Y; Huang JH; Shen X; Hu Q; Tang CJ; Li L
Org Lett; 2002 Jun; 4(13):2141-4. PubMed ID: 12074652
[TBL] [Abstract][Full Text] [Related]
11. KHF
Lakshman MK; Tine FA; Khandaker TA; Basava V; Agyemang NB; Benavidez MSA; Gaši M; Guerrera L; Zajc B
Synlett; 2017 Mar; 28(3):381-385. PubMed ID: 28713205
[TBL] [Abstract][Full Text] [Related]
12. Continuous-/Micro-Flow Reactions Using Highly Electrophilic PCl
Kitamura H; Fuse S
Chempluschem; 2023 Jun; 88(6):e202300176. PubMed ID: 37222183
[TBL] [Abstract][Full Text] [Related]
13. Synthesis and Applications of Silyl 2-Methylprop-2-ene-1-sulfinates in Preparative Silylation and GC-Derivatization Reactions of Polyols and Carbohydrates.
Marković D; Tchawou WA; Novosjolova I; Laclef S; Stepanovs D; Turks M; Vogel P
Chemistry; 2016 Mar; 22(12):4196-205. PubMed ID: 26864218
[TBL] [Abstract][Full Text] [Related]
14. Regioselective silylation of N-phthaloylchitosan with TBDMS and TBDPS groups.
Binette A; Gagnon J
Biomacromolecules; 2007 Jun; 8(6):1812-5. PubMed ID: 17487971
[TBL] [Abstract][Full Text] [Related]
15. Catalytic Vilsmeier-Haack Reactions for C1-Deuterated Formylation of Indoles.
Xue J; Zhang YS; Huan Z; Yang JD; Cheng JP
J Org Chem; 2022 Nov; 87(22):15539-15546. PubMed ID: 36348629
[TBL] [Abstract][Full Text] [Related]
16. Synthesis of gamma-aminobutyric acid analogs based on carbohydrate scaffolds.
Zhong M; Meng XB; Li ZJ
Carbohydr Res; 2010 Jun; 345(9):1099-106. PubMed ID: 20400064
[TBL] [Abstract][Full Text] [Related]
17. Efficient method for the deprotection of tert-butyldimethylsilyl ethers with TiCl4-Lewis base complexes: application to the synthesis of 1beta-methylcarbapenems.
Iida A; Okazaki H; Misaki T; Sunagawa M; Sasaki A; Tanabe Y
J Org Chem; 2006 Jul; 71(14):5380-3. PubMed ID: 16808532
[TBL] [Abstract][Full Text] [Related]
18. A new, simple, and selective palladium-catalyzed cleavage of triethylsilyl ethers.
Rotulo-Sims D; Prunet J
Org Lett; 2002 Dec; 4(26):4701-4. PubMed ID: 12489965
[TBL] [Abstract][Full Text] [Related]
19. Regioselective and stereospecific acylation across oxirane- and silyloxy systems as a novel strategy to the synthesis of enantiomerically pure mono-, di- and triglycerides.
Stamatov SD; Stawinski J
Org Biomol Chem; 2007 Dec; 5(23):3787-800. PubMed ID: 18004458
[TBL] [Abstract][Full Text] [Related]
20. tert-Butyldimethylsilyl O-protected chitosan and chitooligosaccharides: useful precursors for N-modifications in common organic solvents.
Rúnarsson OV; Malainer C; Holappa J; Sigurdsson ST; Másson M
Carbohydr Res; 2008 Oct; 343(15):2576-82. PubMed ID: 18768174
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
