Works about ACYLALS

Results: 9

Synthesis of sulfonated carbon-based solid acid as a novel and efficient nanocatalyst for the preparation of highly functionalized piperidines and acylals: a DFT study.

Published in:

Research on Chemical Intermediates, 2016, v. 42, n. 6, p. 6105, doi. 10.1007/s11164-016-2448-4

By:

Hoseinabadi, Zahra;
Pourmousavi, Seied;
Zamani, Mahdi

Publication type:

Article

Synthesis of geminal dinitro derivatives of cycloalka[ b]pyridin-2-one.

Published in:

Russian Journal of Organic Chemistry, 2016, v. 52, n. 6, p. 827, doi. 10.1134/S1070428016060105

By:

Ershov, O.;
Tafeenko, V.;
Fedoseev, S.;
Eremkin, A.;
Nasakin, O.

Publication type:

Article

NaBH4/Ac2O/DOWEX(R)50WX4: A Convenient System for Fast Preparation of gem-Diacetates from Aldehydes.

Published in:

Journal of the Chinese Chemical Society, 2014, v. 61, n. 8, p. 940, doi. 10.1002/jccs.201400049

By:

Asl, Parisa Azizi;
Setamdideh, Davood

Publication type:

Article

Synthesis and Conformational Analysis of 1:1 [α/α‐Nα‐Bn‐Hydrazino] and 1:1 [α‐Nα‐Bn‐Hydrazino/α] Trimers: Determination of the Δδ Value for the γ‐Turn Structuration

Published in:

European Journal of Organic Chemistry, 2018, v. 2018, n. 34, p. 4754, doi. 10.1002/ejoc.201800755

By:

Romero, Eugénie;
Moussodia, Ralph‐Olivier;
Jamart‐Grégoire, Brigitte;
Acherar, Samir

Publication type:

Article

Molecular Properties of Additive Poly(bis(trimethylsilyl)tricyclonones) with Vicinal and Geminal Side Substituents.

Published in:

Polymer Science -- Series A, 2018, v. 60, n. 2, p. 162, doi. 10.1134/S0965545X18020050

By:

Yevlampieva, N. P.;
Bermeshev, M. V.;
Vezo, O. S.;
Chapala, P. P.;
Il’yasova, Yu. V.

Publication type:

Article

Green procedures for the chemoselective synthesis of acylals and their cleavage promoted by recoverable sulfonic acid based nanoporous carbon (CMK-5-SOH).

Published in:

Journal of Chemical Sciences, 2015, v. 127, n. 7, p. 1229, doi. 10.1007/s12039-015-0884-0

By:

ZAREYEE, DARYOUSH;
MIRZAJANZADEH, EHSAN;
KHALILZADEH, MOHAMMAD

Publication type:

Article

Frontispiece: Short Total Synthesis of (±)-γ-Lycorane by a Sequential Intramolecular Acylal Cyclisation (IAC) and Intramolecular Heck Addition Reaction.

Published in:

Chemistry - A European Journal, 2017, v. 23, n. 20, p. n/a, doi. 10.1002/chem.201782062

By:

Monaco, Alessandra;
Szulc, Blanka R.;
Rao, Zenobia X.;
Barniol‐Xicota, Marta;
Sehailia, Moussa;
Borges, Bruno M. A.;
Hilton, Stephen T.

Publication type:

Article

Intramolecular Acylal Cyclisation (IAC) as an Efficient Synthetic Strategy towards the Total Synthesis of Erythrina Alkaloid Derivatives.

Published in:

Chemistry - A European Journal, 2015, v. 21, n. 40, p. 13909, doi. 10.1002/chem.201502436

By:

Monaco, Alessandra;
Aliev, Abil E.;
Hilton, Stephen T.

Publication type:

Article

CELLULOSE SULPHURIC ACID (CSA) AS A BIODEGRADABLE, RECYCLABLE CATALYST FOR AN EFFICIENT FORMATION OF CARBON-SULPHUR BOND: EXPLORED THROUGH THE TRANSTHIOACETALIZATION OF ACETALS AND ACYLALS.

Published in:

Journal of Advanced Scientific Research, 2020, v. 11, n. 3, p. 281

By:

Kadam, Kailas R.

Publication type:

Article

Works about ACYLALS

Synthesis of sulfonated carbon-based solid acid as a novel and efficient nanocatalyst for the preparation of highly functionalized piperidines and acylals: a DFT study.

Synthesis of geminal dinitro derivatives of cycloalka[ b]pyridin-2-one.

NaBH<sub>4</sub>/Ac<sub>2</sub>O/DOWEX(R)50WX4: A Convenient System for Fast Preparation of gem-Diacetates from Aldehydes.

Synthesis and Conformational Analysis of 1:1 [α/α‐N<sup>α</sup>‐Bn‐Hydrazino] and 1:1 [α‐N<sup>α</sup>‐Bn‐Hydrazino/α] Trimers: Determination of the Δδ Value for the γ‐Turn Structuration

Molecular Properties of Additive Poly(bis(trimethylsilyl)tricyclonones) with Vicinal and Geminal Side Substituents.

Green procedures for the chemoselective synthesis of acylals and their cleavage promoted by recoverable sulfonic acid based nanoporous carbon (CMK-5-SOH).

Frontispiece: Short Total Synthesis of (±)-γ-Lycorane by a Sequential Intramolecular Acylal Cyclisation (IAC) and Intramolecular Heck Addition Reaction.

Intramolecular Acylal Cyclisation (IAC) as an Efficient Synthetic Strategy towards the Total Synthesis of Erythrina Alkaloid Derivatives.

CELLULOSE SULPHURIC ACID (CSA) AS A BIODEGRADABLE, RECYCLABLE CATALYST FOR AN EFFICIENT FORMATION OF CARBON-SULPHUR BOND: EXPLORED THROUGH THE TRANSTHIOACETALIZATION OF ACETALS AND ACYLALS.