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The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues.

Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid

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The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues. / Coxon, GD; Knobl, S; Roberts, E et al.
Yn: Tetrahedron Letters, Cyfrol 40, Rhif 36, 03.09.1999, t. 6689-6692.

Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid

HarvardHarvard

Coxon, GD, Knobl, S, Roberts, E, Baird, MS, Al Dulayymi, JR, Besra, GS, Brennan, PJ & Minnikin, DE 1999, 'The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues.', Tetrahedron Letters, cyfrol. 40, rhif 36, tt. 6689-6692. https://doi.org/10.1016/S0040-4039(99)01378-7

APA

Coxon, GD., Knobl, S., Roberts, E., Baird, MS., Al Dulayymi, JR., Besra, GS., Brennan, PJ., & Minnikin, DE. (1999). The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues. Tetrahedron Letters, 40(36), 6689-6692. https://doi.org/10.1016/S0040-4039(99)01378-7

CBE

Coxon GD, Knobl S, Roberts E, Baird MS, Al Dulayymi JR, Besra GS, Brennan PJ, Minnikin DE. 1999. The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues. Tetrahedron Letters. 40(36):6689-6692. https://doi.org/10.1016/S0040-4039(99)01378-7

MLA

Coxon, GD et al. "The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues.". Tetrahedron Letters. 1999, 40(36). 6689-6692. https://doi.org/10.1016/S0040-4039(99)01378-7

VancouverVancouver

Coxon GD, Knobl S, Roberts E, Baird MS, Al Dulayymi JR, Besra GS et al. The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues. Tetrahedron Letters. 1999 Medi 3;40(36):6689-6692. doi: 10.1016/S0040-4039(99)01378-7

Author

Coxon, GD ; Knobl, S ; Roberts, E et al. / The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues. Yn: Tetrahedron Letters. 1999 ; Cyfrol 40, Rhif 36. tt. 6689-6692.

RIS

TY - JOUR

T1 - The synthesis of both enantiomers of lactobacillic acid and mycolic acid analogues.

AU - Coxon, GD

AU - Knobl, S

AU - Roberts, E

AU - Baird, MS

AU - Al Dulayymi, JR

AU - Besra, GS

AU - Brennan, PJ

AU - Minnikin, DE

PY - 1999/9/3

Y1 - 1999/9/3

N2 - (11R, 12S)-lactobacillic acid (1) has been prepared either from D-mannitol by asymmetric cyclopropanation or from cycyclopropane-1, 2-dimethanol by enzymatic desymmetrisation. The syntheses of (11S, 12R)-lactobacillic acid (2) and (1R, 2S) 1(3'-methoxycarbonylpropyl)-2-octadecylcopropane (26) and related analogues (27 and 28) have also been achieved. (C) 1999 Elsevier Science Ltd. All rights reserved.

AB - (11R, 12S)-lactobacillic acid (1) has been prepared either from D-mannitol by asymmetric cyclopropanation or from cycyclopropane-1, 2-dimethanol by enzymatic desymmetrisation. The syntheses of (11S, 12R)-lactobacillic acid (2) and (1R, 2S) 1(3'-methoxycarbonylpropyl)-2-octadecylcopropane (26) and related analogues (27 and 28) have also been achieved. (C) 1999 Elsevier Science Ltd. All rights reserved.

U2 - 10.1016/S0040-4039(99)01378-7

DO - 10.1016/S0040-4039(99)01378-7

M3 - Article

VL - 40

SP - 6689

EP - 6692

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 36

ER -