Literature DB >> 21202537

2-O-Benzhydryl-3,4-(S)-O-benzyl-idene-d-xylono-1,4-lactone.

Sarah F Jenkinson, Sebastian D Rule, Kathrine V Booth, George W J Fleet, David J Watkin, Sigthor Petursson.   

Abstract

X-ray crystallography unequivocally shows that protection of the free hydroxyl group of 3,5-O-benzyl-idene-d-xylono-1,4-lactone with diphenyl-diazo-methane proceeded smoothly to give the title compound, C(25)H(22)O(5), with no accompanying epimerization. Unlike the analogously protected lyxono lactone, the isomeric xylono lactone has two mol-ecules present in the asymmetric unit (Z' = 2). The 5-ring lactones adopt envelope conformations and the 6-ring ketals adopt chair conformations.

Entities:  

Year:  2008        PMID: 21202537      PMCID: PMC2961596          DOI: 10.1107/S1600536808012567

Source DB:  PubMed          Journal:  Acta Crystallogr Sect E Struct Rep Online        ISSN: 1600-5368


Related literature

For related literature, see: Collins & Ferrier (1995 ▶); Draths et al. (1992 ▶); Jackson et al. (1982 ▶); Petursson & Webber (1982 ▶); Petursson et al. (2007 ▶); Petursson (2001 ▶, 2003 ▶); Best et al. (2008 ▶); Jenkinson et al. (2008 ▶); Görbitz (1999 ▶).

Experimental

Crystal data

C25H22O5 M = 402.45 Monoclinic, a = 14.8159 (3) Å b = 9.1959 (2) Å c = 15.0797 (2) Å β = 93.7245 (12)° V = 2050.20 (7) Å3 Z = 4 Mo Kα radiation μ = 0.09 mm−1 T = 150 K 0.80 × 0.30 × 0.10 mm

Data collection

Nonius KappaCCD area-detector diffractometer Absorption correction: multi-scan (DENZO/SCALEPACK; Otwinowski & Minor, 1997 ▶) T min = 0.55, T max = 0.99 25081 measured reflections 4938 independent reflections 3950 reflections with I > 2σ(I) R int = 0.047

Refinement

R[F 2 > 2σ(F 2)] = 0.034 wR(F 2) = 0.101 S = 0.89 4938 reflections 542 parameters 1 restraint H-atom parameters constrained Δρmax = 0.25 e Å−3 Δρmin = −0.27 e Å−3 Data collection: COLLECT (Nonius, 2001 ▶).; cell refinement: DENZO/SCALEPACK (Otwinowski & Minor, 1997 ▶); data reduction: DENZO/SCALEPACK; program(s) used to solve structure: SIR92 (Altomare et al., 1994 ▶); program(s) used to refine structure: CRYSTALS (Betteridge et al., 2003 ▶); molecular graphics: CAMERON (Watkin et al., 1996 ▶); software used to prepare material for publication: CRYSTALS. Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536808012567/lh2623sup1.cif Structure factors: contains datablocks I. DOI: 10.1107/S1600536808012567/lh2623Isup2.hkl Additional supplementary materials: crystallographic information; 3D view; checkCIF report
C25H22O5F000 = 848
Mr = 402.45Dx = 1.304 Mg m3
Monoclinic, P21Mo Kα radiation λ = 0.71073 Å
Hall symbol: P 2ybCell parameters from 4834 reflections
a = 14.8159 (3) Åθ = 5–27º
b = 9.1959 (2) ŵ = 0.09 mm1
c = 15.0797 (2) ÅT = 150 K
β = 93.7245 (12)ºPlate, colourless
V = 2050.20 (7) Å30.80 × 0.30 × 0.10 mm
Z = 4
Nonius KappaCCD area-detector diffractometer3950 reflections with I > 2σ(I)
Monochromator: graphiteRint = 0.047
T = 150 Kθmax = 27.5º
ω scansθmin = 5.2º
Absorption correction: multi-scan(DENZO/SCALEPACK; Otwinowski & Minor, 1997)h = −19→19
Tmin = 0.55, Tmax = 0.99k = −11→11
25081 measured reflectionsl = −19→19
4938 independent reflections
Refinement on F2Hydrogen site location: inferred from neighbouring sites
Least-squares matrix: fullH-atom parameters constrained
R[F2 > 2σ(F2)] = 0.034  Method, part 1, Chebychev polynomial, (Watkin, 1994, Prince, 1982) [weight] = 1.0/[A0*T0(x) + A1*T1(x) ··· + An-1]*Tn-1(x)] where Ai are the Chebychev coefficients listed below and x = F /Fmax Method = Robust Weighting (Prince, 1982) W = [weight] * [1-(deltaF/6*sigmaF)2]2 Ai are: 16.9 24.9 12.6 3.46
wR(F2) = 0.101(Δ/σ)max = 0.0003
S = 0.89Δρmax = 0.25 e Å3
4938 reflectionsΔρmin = −0.27 e Å3
542 parametersExtinction correction: Larson (1970), Equation 22
1 restraintExtinction coefficient: 600 (50)
Primary atom site location: structure-invariant direct methods
xyzUiso*/Ueq
O10.44166 (10)0.5327 (2)0.31715 (10)0.0244
C20.40499 (15)0.5336 (3)0.22694 (15)0.0242
C30.30725 (16)0.4866 (3)0.23203 (15)0.0254
O40.25857 (10)0.5219 (2)0.15093 (10)0.0265
C50.16129 (15)0.5192 (3)0.15751 (16)0.0257
C60.13142 (16)0.6490 (3)0.21052 (15)0.0252
C70.17991 (18)0.7781 (3)0.21395 (18)0.0330
C80.1517 (2)0.8947 (3)0.26476 (19)0.0403
C90.0760 (2)0.8806 (3)0.31222 (18)0.0432
C100.0264 (2)0.7539 (4)0.30826 (19)0.0437
C110.05367 (19)0.6375 (3)0.25762 (17)0.0335
C120.12135 (15)0.5140 (3)0.06274 (15)0.0255
C130.15139 (19)0.6107 (3)0.00038 (17)0.0339
C140.1185 (2)0.6028 (4)−0.08784 (18)0.0429
C150.0551 (2)0.4987 (4)−0.11333 (19)0.0486
C160.02472 (19)0.4030 (4)−0.0519 (2)0.0479
C170.05739 (17)0.4106 (4)0.03651 (19)0.0368
C180.31556 (18)0.3212 (3)0.23435 (18)0.0323
O190.26098 (14)0.2338 (2)0.25627 (16)0.0478
O200.39494 (13)0.2813 (2)0.20131 (13)0.0344
C210.44429 (17)0.4094 (3)0.17435 (16)0.0296
C220.54422 (17)0.3886 (3)0.19447 (16)0.0335
O230.56825 (11)0.3965 (2)0.28758 (11)0.0301
C240.53776 (15)0.5268 (3)0.32352 (15)0.0255
C250.56837 (16)0.5320 (3)0.42104 (16)0.0277
C260.53029 (17)0.6335 (3)0.47592 (17)0.0318
C270.5559 (2)0.6362 (4)0.56635 (19)0.0417
C280.6204 (2)0.5396 (4)0.6014 (2)0.0479
C290.6607 (2)0.4425 (4)0.5464 (2)0.0479
C300.63432 (19)0.4375 (3)0.45597 (19)0.0359
O1010.17514 (11)0.3628 (2)0.56763 (10)0.0280
C1020.26545 (16)0.3497 (3)0.60615 (15)0.0265
C1030.26225 (16)0.3956 (3)0.70212 (16)0.0266
O1040.34196 (11)0.3412 (2)0.74916 (10)0.0274
C1050.33862 (16)0.3463 (3)0.84483 (15)0.0254
C1060.27885 (16)0.2264 (3)0.87746 (17)0.0275
C1070.25628 (19)0.1047 (3)0.82618 (19)0.0368
C1080.2043 (2)−0.0056 (4)0.8592 (2)0.0473
C1090.17436 (19)0.0054 (4)0.9435 (3)0.0506
C1100.1966 (2)0.1261 (4)0.9956 (2)0.0512
C1110.2483 (2)0.2372 (4)0.9627 (2)0.0394
C1120.43660 (16)0.3392 (3)0.88150 (15)0.0254
C1130.49799 (18)0.4396 (3)0.85136 (18)0.0320
C1140.58750 (19)0.4422 (3)0.8863 (2)0.0383
C1150.61626 (18)0.3427 (3)0.95059 (18)0.0348
C1160.55682 (18)0.2406 (3)0.97998 (16)0.0318
C1170.46694 (17)0.2387 (3)0.94582 (15)0.0276
C1180.27224 (17)0.5609 (3)0.69587 (17)0.0307
O1190.25584 (16)0.6510 (3)0.75019 (14)0.0446
O1200.30885 (13)0.5960 (2)0.61933 (12)0.0333
C1210.32735 (16)0.4648 (3)0.56966 (16)0.0299
C1220.30971 (17)0.4926 (4)0.47132 (17)0.0357
O1230.21497 (11)0.4979 (2)0.44632 (11)0.0315
C1240.17243 (16)0.3695 (3)0.47308 (15)0.0280
C1250.07503 (16)0.3717 (3)0.43830 (16)0.0286
C1260.01418 (18)0.4674 (3)0.47230 (17)0.0354
C127−0.07582 (19)0.4661 (4)0.44074 (19)0.0426
C128−0.10512 (19)0.3684 (4)0.3750 (2)0.0417
C129−0.0444 (2)0.2749 (4)0.3393 (2)0.0412
C1300.0462 (2)0.2761 (3)0.37099 (18)0.0344
H210.41020.63080.19800.0310*
H310.28150.52920.28380.0300*
H510.14610.42850.19120.0293*
H710.23320.78970.17930.0378*
H810.18540.98280.26570.0498*
H910.05740.95860.34620.0522*
H101−0.02700.74560.34170.0499*
H1110.01930.55070.25590.0398*
H1310.19440.68310.01550.0428*
H1410.14170.6660−0.13050.0511*
H1510.02930.4918−0.17220.0598*
H161−0.01950.3290−0.06680.0570*
H1710.03840.34460.07680.0465*
H2110.43120.42570.10740.0355*
H2210.57800.46290.15870.0427*
H2220.56170.28960.17660.0439*
H2410.56270.61050.29090.0328*
H2610.48460.70130.45430.0393*
H2710.52980.70650.60430.0510*
H2810.63720.54190.66400.0566*
H2910.70870.37650.57040.0512*
H3010.66220.36860.41990.0430*
H10210.29090.25130.59390.0322*
H10310.20660.36710.73080.0308*
H10510.31310.44490.85890.0297*
H10710.27550.09770.76830.0447*
H10810.1886−0.09040.82410.0582*
H10910.1414−0.06920.96760.0609*
H11010.17770.13341.05310.0637*
H11110.26190.32110.99670.0452*
H11310.47900.50640.80200.0373*
H11410.62880.51140.86310.0459*
H11510.67690.34370.97450.0399*
H11610.57880.16941.02260.0391*
H11710.42230.16780.96520.0343*
H12110.39140.43810.58510.0389*
H12210.33780.58730.45630.0426*
H12220.33940.41380.43830.0433*
H12410.20310.28340.45060.0363*
H12610.03400.53260.51870.0406*
H1271−0.11840.53050.46600.0513*
H1281−0.16770.36700.35520.0470*
H1291−0.06490.21010.29290.0471*
H13010.08950.21050.34570.0399*
U11U22U33U12U13U23
O10.0232 (7)0.0288 (9)0.0210 (7)−0.0002 (7)0.0005 (6)−0.0019 (7)
C20.0265 (11)0.0255 (12)0.0202 (10)0.0009 (9)−0.0007 (8)0.0009 (9)
C30.0275 (11)0.0277 (13)0.0209 (10)−0.0006 (10)−0.0001 (8)0.0048 (10)
O40.0243 (8)0.0340 (10)0.0209 (7)0.0030 (7)−0.0011 (6)0.0044 (7)
C50.0245 (11)0.0251 (12)0.0276 (11)−0.0001 (10)0.0017 (8)0.0027 (10)
C60.0300 (11)0.0240 (11)0.0211 (10)0.0031 (10)−0.0022 (8)0.0024 (9)
C70.0352 (13)0.0288 (13)0.0346 (13)−0.0016 (11)−0.0004 (10)−0.0027 (11)
C80.0518 (16)0.0289 (14)0.0387 (14)−0.0017 (13)−0.0081 (12)−0.0037 (12)
C90.0659 (19)0.0334 (16)0.0298 (13)0.0140 (15)0.0001 (12)−0.0040 (12)
C100.0570 (18)0.0398 (17)0.0361 (15)0.0146 (14)0.0169 (13)0.0055 (13)
C110.0390 (13)0.0283 (13)0.0341 (13)0.0044 (11)0.0094 (10)0.0046 (11)
C120.0239 (10)0.0255 (12)0.0269 (11)0.0055 (9)−0.0005 (8)−0.0051 (10)
C130.0413 (14)0.0298 (14)0.0296 (12)−0.0048 (11)−0.0048 (10)−0.0012 (11)
C140.0528 (17)0.0505 (18)0.0244 (13)0.0027 (15)−0.0041 (11)0.0001 (13)
C150.0420 (15)0.072 (2)0.0303 (13)0.0034 (16)−0.0085 (11)−0.0144 (16)
C160.0305 (13)0.066 (2)0.0468 (16)−0.0103 (15)−0.0029 (11)−0.0195 (17)
C170.0269 (12)0.0416 (16)0.0422 (14)−0.0072 (12)0.0034 (10)−0.0072 (13)
C180.0321 (13)0.0315 (14)0.0318 (13)−0.0024 (11)−0.0098 (10)0.0067 (11)
O190.0394 (11)0.0384 (12)0.0638 (14)−0.0101 (10)−0.0106 (10)0.0201 (11)
O200.0399 (10)0.0248 (9)0.0376 (10)0.0003 (8)−0.0035 (8)−0.0012 (8)
C210.0357 (12)0.0308 (13)0.0223 (10)0.0026 (11)0.0027 (9)−0.0005 (10)
C220.0373 (13)0.0370 (14)0.0267 (12)0.0071 (12)0.0052 (10)−0.0038 (11)
O230.0300 (8)0.0340 (10)0.0264 (8)0.0074 (8)0.0021 (6)−0.0025 (8)
C240.0224 (10)0.0262 (12)0.0282 (11)0.0001 (10)0.0032 (8)−0.0014 (10)
C250.0245 (11)0.0280 (12)0.0303 (12)−0.0073 (10)−0.0004 (9)−0.0015 (10)
C260.0289 (12)0.0327 (14)0.0336 (13)−0.0030 (11)0.0009 (9)−0.0074 (11)
C270.0428 (15)0.0469 (18)0.0350 (14)−0.0127 (14)−0.0017 (11)−0.0100 (14)
C280.0585 (19)0.0486 (18)0.0344 (14)−0.0137 (16)−0.0135 (13)−0.0068 (14)
C290.0542 (18)0.0407 (18)0.0456 (17)0.0004 (15)−0.0219 (14)−0.0023 (14)
C300.0372 (13)0.0318 (14)0.0373 (14)0.0023 (11)−0.0080 (11)−0.0043 (12)
O1010.0258 (8)0.0354 (10)0.0223 (8)−0.0028 (7)−0.0020 (6)0.0045 (7)
C1020.0243 (11)0.0282 (12)0.0268 (11)0.0022 (10)−0.0011 (8)0.0006 (10)
C1030.0230 (10)0.0315 (13)0.0249 (11)0.0045 (10)0.0002 (8)0.0039 (10)
O1040.0251 (8)0.0349 (10)0.0219 (8)0.0045 (7)−0.0009 (6)0.0021 (7)
C1050.0276 (11)0.0253 (12)0.0234 (10)0.0012 (10)0.0017 (8)0.0004 (10)
C1060.0224 (11)0.0293 (13)0.0309 (12)0.0040 (10)0.0017 (9)0.0040 (10)
C1070.0379 (14)0.0348 (15)0.0367 (14)−0.0038 (12)−0.0050 (11)0.0054 (12)
C1080.0436 (16)0.0373 (17)0.0591 (19)−0.0105 (14)−0.0108 (13)0.0091 (15)
C1090.0315 (14)0.0453 (19)0.075 (2)0.0004 (13)0.0064 (14)0.0245 (18)
C1100.0442 (17)0.052 (2)0.060 (2)0.0125 (16)0.0272 (15)0.0164 (17)
C1110.0377 (14)0.0385 (16)0.0435 (15)0.0096 (13)0.0152 (12)0.0036 (13)
C1120.0268 (11)0.0262 (12)0.0230 (10)0.0003 (10)0.0003 (8)−0.0033 (9)
C1130.0333 (12)0.0267 (13)0.0356 (13)−0.0018 (10)−0.0012 (10)0.0016 (11)
C1140.0342 (14)0.0329 (15)0.0473 (15)−0.0060 (12)−0.0002 (11)−0.0029 (13)
C1150.0284 (12)0.0387 (15)0.0363 (13)0.0009 (11)−0.0051 (10)−0.0111 (12)
C1160.0329 (13)0.0377 (15)0.0239 (11)0.0081 (11)−0.0051 (9)−0.0038 (11)
C1170.0307 (12)0.0303 (13)0.0215 (10)0.0026 (10)0.0008 (9)−0.0010 (10)
C1180.0294 (12)0.0332 (14)0.0291 (12)0.0039 (10)−0.0005 (9)0.0015 (11)
O1190.0597 (13)0.0362 (11)0.0382 (10)0.0110 (10)0.0052 (9)−0.0041 (10)
O1200.0381 (10)0.0317 (10)0.0304 (9)−0.0055 (8)0.0030 (7)0.0035 (8)
C1210.0255 (11)0.0375 (14)0.0268 (11)−0.0026 (11)0.0028 (9)−0.0006 (11)
C1220.0268 (12)0.0527 (18)0.0278 (12)−0.0056 (12)0.0041 (9)0.0032 (13)
O1230.0274 (8)0.0407 (11)0.0264 (8)−0.0048 (8)0.0019 (6)0.0068 (8)
C1240.0308 (11)0.0300 (13)0.0231 (11)−0.0002 (10)0.0019 (9)0.0024 (10)
C1250.0297 (12)0.0313 (13)0.0247 (11)−0.0025 (10)0.0010 (9)0.0040 (10)
C1260.0334 (13)0.0430 (16)0.0294 (12)0.0014 (12)−0.0004 (10)−0.0060 (12)
C1270.0342 (13)0.0577 (19)0.0359 (14)0.0035 (14)0.0024 (11)0.0010 (14)
C1280.0325 (13)0.0510 (19)0.0407 (14)−0.0064 (13)−0.0058 (11)0.0092 (14)
C1290.0456 (16)0.0385 (16)0.0380 (14)−0.0092 (13)−0.0091 (12)−0.0012 (13)
C1300.0420 (14)0.0284 (13)0.0319 (13)−0.0018 (12)−0.0050 (11)−0.0005 (11)
O1—C21.432 (3)O101—C1021.429 (3)
O1—C241.422 (3)O101—C1241.425 (3)
C2—C31.518 (3)C102—C1031.511 (3)
C2—C211.527 (4)C102—C1211.526 (4)
C2—H211.000C102—H10211.002
C3—O41.416 (3)C103—O1041.428 (3)
C3—C181.526 (4)C103—C1181.531 (4)
C3—H310.973C103—H10310.991
O4—C51.451 (3)O104—C1051.448 (3)
C5—C61.518 (3)C105—C1061.516 (3)
C5—C121.512 (3)C105—C1121.521 (3)
C5—H511.009C105—H10511.011
C6—C71.387 (4)C106—C1071.388 (4)
C6—C111.396 (3)C106—C1111.393 (4)
C7—C81.398 (4)C107—C1081.385 (4)
C7—H710.980C107—H10710.938
C8—C91.374 (4)C108—C1091.377 (5)
C8—H810.952C108—H10810.963
C9—C101.377 (5)C109—C1101.387 (5)
C9—H910.933C109—H10910.930
C10—C111.390 (4)C110—C1111.388 (5)
C10—H1010.969C110—H11010.932
C11—H1110.947C111—H11110.941
C12—C131.388 (4)C112—C1131.393 (4)
C12—C171.382 (4)C112—C1171.393 (3)
C13—C141.389 (4)C113—C1141.395 (4)
C13—H1310.939C113—H11310.991
C14—C151.378 (5)C114—C1151.381 (4)
C14—H1410.948C114—H11410.964
C15—C161.374 (5)C115—C1161.380 (4)
C15—H1510.946C115—H11510.946
C16—C171.390 (4)C116—C1171.396 (3)
C16—H1610.961C116—H11610.960
C17—H1710.916C117—H11710.986
C18—O191.202 (3)C118—O1191.201 (3)
C18—O201.357 (3)C118—O1201.346 (3)
O20—C211.458 (3)O120—C1211.456 (3)
C21—C221.504 (4)C121—C1221.511 (3)
C21—H2111.026C121—H12110.994
C22—O231.428 (3)C122—O1231.430 (3)
C22—H2211.021C122—H12210.998
C22—H2220.989C122—H12220.998
O23—C241.402 (3)O123—C1241.409 (3)
C24—C251.511 (3)C124—C1251.503 (3)
C24—H2410.997C124—H12410.984
C25—C261.392 (4)C125—C1261.382 (4)
C25—C301.385 (4)C125—C1301.389 (4)
C26—C271.392 (4)C126—C1271.387 (4)
C26—H2610.961C126—H12610.953
C27—C281.385 (5)C127—C1281.386 (5)
C27—H2710.961C127—H12710.962
C28—C291.380 (5)C128—C1291.379 (5)
C28—H2810.962C128—H12810.955
C29—C301.394 (4)C129—C1301.394 (4)
C29—H2910.986C129—H12910.954
C30—H3010.948C130—H13010.977
C2—O1—C24112.39 (17)C102—O101—C124112.03 (17)
O1—C2—C3104.75 (18)O101—C102—C103106.20 (18)
O1—C2—C21110.80 (19)O101—C102—C121111.3 (2)
C3—C2—C21102.2 (2)C103—C102—C121102.0 (2)
O1—C2—H21112.6O101—C102—H1021110.8
C3—C2—H21112.2C103—C102—H1021117.7
C21—C2—H21113.5C121—C102—H1021108.5
C2—C3—O4108.98 (18)C102—C103—O104107.53 (19)
C2—C3—C18102.1 (2)C102—C103—C118102.1 (2)
O4—C3—C18106.5 (2)O104—C103—C118107.4 (2)
C2—C3—H31110.6C102—C103—H1031115.0
O4—C3—H31113.3O104—C103—H1031112.1
C18—C3—H31114.7C118—C103—H1031112.1
C3—O4—C5112.91 (17)C103—O104—C105113.76 (17)
O4—C5—C6110.32 (19)O104—C105—C106111.0 (2)
O4—C5—C12105.39 (18)O104—C105—C112105.51 (17)
C6—C5—C12114.4 (2)C106—C105—C112114.5 (2)
O4—C5—H51107.6O104—C105—H1051106.0
C6—C5—H51107.6C106—C105—H1051110.5
C12—C5—H51111.3C112—C105—H1051108.9
C5—C6—C7121.7 (2)C105—C106—C107122.0 (2)
C5—C6—C11119.1 (2)C105—C106—C111118.6 (2)
C7—C6—C11119.2 (2)C107—C106—C111119.4 (3)
C6—C7—C8120.3 (3)C106—C107—C108120.6 (3)
C6—C7—H71120.5C106—C107—H1071119.8
C8—C7—H71119.2C108—C107—H1071119.6
C7—C8—C9119.7 (3)C107—C108—C109119.9 (3)
C7—C8—H81119.1C107—C108—H1081121.1
C9—C8—H81121.2C109—C108—H1081119.0
C8—C9—C10120.6 (3)C108—C109—C110120.1 (3)
C8—C9—H91119.5C108—C109—H1091121.1
C10—C9—H91119.9C110—C109—H1091118.7
C9—C10—C11120.1 (3)C109—C110—C111120.2 (3)
C9—C10—H101119.7C109—C110—H1101120.7
C11—C10—H101120.1C111—C110—H1101119.1
C6—C11—C10120.0 (3)C106—C111—C110119.8 (3)
C6—C11—H111120.7C106—C111—H1111119.4
C10—C11—H111119.3C110—C111—H1111120.8
C5—C12—C13119.8 (2)C105—C112—C113118.8 (2)
C5—C12—C17120.8 (2)C105—C112—C117122.6 (2)
C13—C12—C17119.4 (2)C113—C112—C117118.6 (2)
C12—C13—C14120.5 (3)C112—C113—C114120.9 (3)
C12—C13—H131122.2C112—C113—H1131119.8
C14—C13—H131117.3C114—C113—H1131119.2
C13—C14—C15119.6 (3)C113—C114—C115119.7 (3)
C13—C14—H141119.9C113—C114—H1141119.0
C15—C14—H141120.5C115—C114—H1141121.2
C14—C15—C16120.3 (3)C114—C115—C116120.1 (2)
C14—C15—H151122.4C114—C115—H1151120.3
C16—C15—H151117.4C116—C115—H1151119.6
C15—C16—C17120.4 (3)C115—C116—C117120.2 (2)
C15—C16—H161122.9C115—C116—H1161118.9
C17—C16—H161116.7C117—C116—H1161120.8
C16—C17—C12119.9 (3)C116—C117—C112120.3 (2)
C16—C17—H171120.0C116—C117—H1171122.7
C12—C17—H171120.0C112—C117—H1171116.9
C3—C18—O19128.2 (3)C103—C118—O119128.2 (3)
C3—C18—O20109.4 (2)C103—C118—O120109.7 (2)
O19—C18—O20122.3 (3)O119—C118—O120122.0 (3)
C18—O20—C21110.2 (2)C118—O120—C121110.0 (2)
C2—C21—O20104.14 (18)C102—C121—O120104.57 (19)
C2—C21—C22113.2 (2)C102—C121—C122113.7 (2)
O20—C21—C22110.3 (2)O120—C121—C122109.8 (2)
C2—C21—H211110.3C102—C121—H1211109.4
O20—C21—H211109.0O120—C121—H1211107.1
C22—C21—H211109.7C122—C121—H1211111.9
C21—C22—O23111.80 (19)C121—C122—O123111.63 (19)
C21—C22—H221108.5C121—C122—H1221108.8
O23—C22—H221112.7O123—C122—H1221109.1
C21—C22—H222109.5C121—C122—H1222108.2
O23—C22—H222105.2O123—C122—H1222110.5
H221—C22—H222109.0H1221—C122—H1222108.5
C22—O23—C24110.9 (2)C122—O123—C124110.2 (2)
O1—C24—O23110.67 (19)O101—C124—O123109.8 (2)
O1—C24—C25107.49 (18)O101—C124—C125108.28 (18)
O23—C24—C25108.6 (2)O123—C124—C125109.0 (2)
O1—C24—H241109.8O101—C124—H1241109.1
O23—C24—H241109.3O123—C124—H1241110.5
C25—C24—H241111.0C125—C124—H1241110.2
C24—C25—C26119.5 (2)C124—C125—C126120.9 (2)
C24—C25—C30120.7 (2)C124—C125—C130119.3 (2)
C26—C25—C30119.9 (2)C126—C125—C130119.8 (2)
C25—C26—C27120.0 (3)C125—C126—C127120.2 (3)
C25—C26—H261122.5C125—C126—H1261119.7
C27—C26—H261117.5C127—C126—H1261120.0
C26—C27—C28120.0 (3)C126—C127—C128120.0 (3)
C26—C27—H271120.1C126—C127—H1271119.9
C28—C27—H271119.9C128—C127—H1271120.0
C27—C28—C29120.0 (3)C127—C128—C129120.1 (3)
C27—C28—H281119.3C127—C128—H1281119.0
C29—C28—H281120.7C129—C128—H1281121.0
C28—C29—C30120.3 (3)C128—C129—C130120.0 (3)
C28—C29—H291120.5C128—C129—H1291119.4
C30—C29—H291119.2C130—C129—H1291120.7
C29—C30—C25119.8 (3)C129—C130—C125119.9 (3)
C29—C30—H301118.6C129—C130—H1301120.3
C25—C30—H301121.6C125—C130—H1301119.8
D—H···AD—HH···AD···AD—H···A
C8—H81···O19i0.952.573.520 (4)173
C14—H141···O119ii0.952.553.309 (4)137
C28—H281···O19iii0.962.573.225 (4)126
  4 in total

1.  Tin(II) chloride catalyzed reactions of diazodiphenylmethane with vicinal diols in an aprotic solvent. The reactions with cis- and trans-1,2-cyclohexanediols and 1,2-propanediol.

Authors:  Sigthor Petursson
Journal:  Carbohydr Res       Date:  2003-04-22       Impact factor: 2.104

2.  What is the best crystal size for collection of X-ray data? Refinement of the structure of glycyl-L-serine based on data from a very large crystal.

Authors: 
Journal:  Acta Crystallogr B       Date:  1999-12-01

3.  New evidence for the mechanism of the tin(II) chloride catalyzed reactions of vicinal diols with diazodiphenylmethane in 1,2-dimethoxyethane.

Authors:  S Pétursson
Journal:  Carbohydr Res       Date:  2001-04-12       Impact factor: 2.104

4.  2-O-Benzhydryl-3,4-(S)-O-benzyl-idene-d-lyxono-1,4-lactone.

Authors:  Sarah F Jenkinson; Sebastian D Rule; Kathrine V Booth; George W J Fleet; David J Watkin; Sigthor Petursson
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-12-06
  4 in total

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