1,2-diacetals: a new opportunity for organic synthesis.

1,2-diacetals: a new opportunity for organic synthesis.

The use of 1,2-diacetals for a number of synthetic applications to provide diol protection and reactivity control was studied. The chiral versions of these systems were used to desymmetrize the enantiotopic diol pairs and to discriminate diequatorial diols in many carbohydrate derivatives. The fusio...

Volledige beschrijving

Bibliografische gegevens
Hoofdauteurs:	Ley, S, Baeschlin, D, Dixon, D, Foster, A, Ince, S, Priepke, H, Reynolds, D
Formaat:	Journal article
Taal:	English
Gepubliceerd in:	ACS 2001

Gelijkaardige items

A general and efficient procedure for the preparation of enantiopure anti-1,2-diols - synthesis and utility of (R ',R ',S,R)-2,3-butane diacetal protected butane tetrol
door: Dixon, D, et al.
Gepubliceerd in: (1999)

Preparation of desymmetrised meso-tartrate derivatives - synthesis and utility of (R ',R ',R,S)-2,3-butane diacetal protected dimethyl tartrate
door: Dixon, D, et al.
Gepubliceerd in: (1999)

New building blocks for efficient and highly diastereoselective polyol production - Synthesis and utility of (R ',R ',S,S) and (S ',S ',R,R)-2,3-butane diacetal protected butane tetrol derivatives
door: Barlow, J, et al.
Gepubliceerd in: (1999)

The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol
door: Dixon, D, et al.
Gepubliceerd in: (2001)

Butane-2,3-diacetal-desymmetrized glycolic acid—a new building block for the stereoselective synthesis of enantiopure α-hydroxy acids
door: Díez, E, et al.
Gepubliceerd in: (2001)

The use of butane diacetals of glycolic acid as precursors for the synthesis of the phytotoxic calmodulin inhibitor herbarumin II
door: Diez, E, et al.
Gepubliceerd in: (2003)

Total synthesis of the phytotoxic agent herbarumin II using butane diacetals of glycolic acid as building blocks
door: Diez, E, et al.
Gepubliceerd in: (2003)

Synthesis of a ceramide sphingolipid as a potential sex pheromone of the hair crab Erimacrus isenbeckii using butane-2,3-diacetal desymmetrised glycolic acid building blocks
door: Dixon, D, et al.
Gepubliceerd in: (2005)

Highly diastereoselective ketone aldol reactions of butane-2,3-diacetal desymmetrised glycolic acid
door: Dixon, D, et al.
Gepubliceerd in: (2002)

Phenyliodine(III)diacetate (PIDA): Applications in Organic Synthesis
door: Ravi Varala, et al.
Gepubliceerd in: (2022-12-01)

Highly diastereoselective Michael addition reactions of butane-2,3-diacetal desymmetrized glycolic acid. Preparation of alpha-hydroxy-gamma-amino acid derivatives.
door: Dixon, D, et al.
Gepubliceerd in: (2001)

Michael, Michael-aldol and Michael-Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives.
door: Ley, S, et al.
Gepubliceerd in: (2005)

Rapid assembly of anti,anti-1,2,3-triol motifs via stereoselective addition of organometallics to aldehydes obtained from (R ',R ',S,R)-2,3-butane diacetal protected butanetetraol derivatives
door: Dixon, D, et al.
Gepubliceerd in: (2001)

Highly diastereoselective lithium enolate aldol reactions of butane-2,3-diacetal desymmetrized glycolic acid and deprotection to enantiopure anti-2,3-dihydroxy esters.
door: Dixon, D, et al.
Gepubliceerd in: (2001)

Preparation of enantiopure butane-2,3-diacetals of glycolic acid and alkylation reactions leading to alpha-hydroxyacid and amide derivatives.
door: Ley, S, et al.
Gepubliceerd in: (2004)

1,2-Diacetates by epoxide ring opening promoted by erbium(III) triflate
door: Renato Dalpozzo, et al.
Gepubliceerd in: (2006-03-01)

Synthesis of New Chiral Amines with a Cyclic 1,2-Diacetal Skeleton Derived from (2R, 3R)-(+)-Tartaric Acid
door: Ana Maria FaÃƒÂsca Phillips, et al.
Gepubliceerd in: (2006-03-01)

Ethynodiol diacetate
door: 982 SIRIM

Benzene-1,3-diacetic acid
door: Mei Zhu
Gepubliceerd in: (2008-09-01)

The total synthesis of the annonaceous acetogenin, muricatetrocin C.
door: Dixon, D, et al.
Gepubliceerd in: (2002)

The total synthesis of the annonaceous acetogenin, muricatetrocin C.
door: Dixon, D, et al.
Gepubliceerd in: (2002)

The total synthesis of the annonaceous acetogenin, muricatetrocin C
door: Dixon, D, et al.
Gepubliceerd in: (2002)

Diacetin (glyceryl diacetate)
door: 8096 British Standards Institution

Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chlorides
door: Ley, S, et al.
Gepubliceerd in: (2004)

Studies on the generation of enolate anions from butane-2,3-diacetal protected glycolic acid derivatives and subsequent highly diastereoselective coupling reactions with aldehydes and acid chlorides.
door: Ley, S, et al.
Gepubliceerd in: (2004)

Diethyl 2,6,11-trioxo-2,3-dihydro-1H-anthra[1,2-d]imidazole-1,3-diacetate
door: Zahra Afrakssou, et al.
Gepubliceerd in: (2011-08-01)

5-Cyano-1,3-phenylene diacetate
door: Bahar Abbassi, et al.
Gepubliceerd in: (2014-06-01)

A short and efficient stereoselective synthesis of the polyhydroxylated macrolactone (+)-aspicillin
door: Dixon, D, et al.
Gepubliceerd in: (2000)

Stabilization and modification of cellulose diacetate /
door: Niyazi, Farukh Fatehovich
Gepubliceerd in: (c200)

(3-Nitrophenyl)methanediyl diacetate
door: Alireza Abbasi, et al.
Gepubliceerd in: (2008-01-01)

<b>Bioassay studies of metal(II) complexes of 2,2'-(ethane-1,2-diyldiimino)diacetic acid</b>
door: Saeed-ur-Rehman, et al.
Gepubliceerd in: (2011-08-01)

1-Benzyl-2,5-dioxopyrrolidine-3,4-diyl diacetate
door: Caracelli, I., et al.
Gepubliceerd in: (2010)

1-Benzyl-2,5-dioxopyrrolidine-3,4-diyl diacetate
door: Edward R. T. Tiekink, et al.
Gepubliceerd in: (2010-12-01)

Facile Conversion of Epoxides to 1,2-Diacetates with NaOAc•3H2O/Ac2O System
door: Masumeh Gilanizadeh, et al.
Gepubliceerd in: (2016-02-01)

Swietenolide diacetate from the seeds of Swietenia macrophylla
door: Goh, B.H., et al.
Gepubliceerd in: (2010)

A short and efficient stereoselective synthesis of the potent 5-lipoxygenase inhibitor, CMI-977
door: Dixon, D, et al.
Gepubliceerd in: (2001)

A short and efficient stereoselective synthesis of the potent 5-lipoxygenase inhibitor, CMI-977
door: Dixon, D, et al.
Gepubliceerd in: (2001)

A short and efficient stereoselective synthesis of the potent 5-lipoxygenase inhibitor CMI-977
door: Dixon, D, et al.
Gepubliceerd in: (2000)

trans-Ethylenedi-p-phenylene diacetate
door: Stefanie Ritter, et al.
Gepubliceerd in: (2009-09-01)

The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C We thank the EPSRC (D.J.D. and D.J.R.), the Novartis Research Fellowship (S.V.L.), and the BP Research Endowment (S.V.L.) for generous financial support for this work.
door: Dixon, D, et al.
Gepubliceerd in: (2000)