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Category:Stereochemistry

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The following 139 pages are in this category, out of 139 total.
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This category has the following 7 subcategories, out of 7 total.
502:Dynamic kinetic resolution in asymmetric synthesis 1021:Tricapped trigonal prismatic molecular geometry 345:Capped square antiprismatic molecular geometry 318:Bicapped trigonal prismatic molecular geometry 8: 350:Capped trigonal prismatic molecular geometry 917:Spontaneous absolute asymmetric synthesis 781:Pentagonal bipyramidal molecular geometry 213:This list may not reflect recent changes 1026:Trigonal bipyramidal molecular geometry 922:Square antiprismatic molecular geometry 1036:Trigonal prismatic molecular geometry 7: 821:Proline isomerization in epigenetics 786:Pentagonal planar molecular geometry 340:Capped octahedral molecular geometry 208:Pages in category "Stereochemistry" 1031:Trigonal planar molecular geometry 534:Enantiomer self-disproportionation 425:Chirality-induced spin selectivity 217: 108: 64: 53: 45: 14: 335:Cahn–Ingold–Prelog priority rules 482:Diastereomeric recrystallization 370:Chiral thin-layer chromatography 18: 497:Dodecahedral molecular geometry 1: 445:Cross-linked enzyme aggregate 1087:Jacobus Henricus van 't Hoff 831:Protein quaternary structure 686:Le Bel–Van 't Hoff rule 365:Chiral column chromatography 264:Antarafacial and suprafacial 836:Protein secondary structure 759:Optical rotatory dispersion 1108: 549:Enantioselective synthesis 32:The main article for this 31: 826:Protein primary structure 375:Chiral derivatizing agent 979:Supramolecular chirality 460:Cyclohexane conformation 435:Conformational isomerism 937:Stereoelectronic effect 708:Molecular configuration 669:Kryptoracemic compounds 507:Dynamic stereochemistry 313:Bent molecular geometry 1077:Subfields of chemistry 927:Staggered conformation 902:Serine octamer cluster 248:Alkane stereochemistry 237:Absolute configuration 984:Syn and anti addition 801:Pirkle's alcohol 764:Orbital hybridisation 630:Homometric structures 524:Eclipsed conformation 415:Chirality (chemistry) 192:Stereochemistry stubs 1048:Van der Waals strain 1001:Thorpe–Ingold effect 791:Pentane interference 455:Cryptoregiochemistry 395:C2-Symmetric ligands 308:Baldwin's rules 281:Asymmetric induction 270:Antipode (chemistry) 846:Pyramidal inversion 664:Klyne–Prelog system 586:Fürst-Plattner Rule 581:Folding (chemistry) 539:Enantiomeric excess 440:Coordination number 430:Cis–trans isomerism 974:Strain (chemistry) 969:Sterimol parameter 776:P-Chiral phosphine 741:Nitrogen inversion 713:Mosher's acid 659:Kinetic resolution 647:Inherent chirality 642:Immobilized enzyme 615:Haworth projection 576:Fischer projection 554:Endo–exo isomerism 420:Chirality timeline 132:Molecular geometry 1082:Organic chemistry 1016:Torquoselectivity 952:Stereospecificity 947:Stereoselectivity 912:Specific rotation 884:Residual topology 735:Newman projection 691:Ligand cone angle 487:Diatomic molecule 400:Chiral resolution 390:Chiral Lewis acid 323:Bredt's rule 276:Asymmetric carbon 88:Enantiopure drugs 1099: 965: 886: 878:Regioselectivity 806:Planar chirality 754:Optical rotation 743: 730:Natta projection 544:Enantiopure drug 472:Desymmetrization 385:Chiral inversion 360:Chiral auxiliary 272: 250: 197: 177: 157: 152:Racemic mixtures 137: 117: 110: 93: 73: 66: 28: 26:Chemistry portal 23: 22: 21: 1107: 1106: 1102: 1101: 1100: 1098: 1097: 1096: 1067: 1066: 1065: 1064: 1063: 1062: 1053:Viedma ripening 1040: 988: 961: 942:Stereoisomerism 894: 882: 863:Racemic mixture 850: 796:Pfeiffer effect 768: 746: 739: 722: 695: 673: 651: 634: 607: 595: 568: 511: 464: 450:Cryptochirality 355:Chiral analysis 327: 295: 291:Axial chirality 268: 246: 229: 225:Stereochemistry 205: 204: 203: 202: 199: 198: 182: 179: 178: 162: 159: 158: 142: 139: 138: 122: 119: 118: 107: 98: 95: 94: 78: 75: 74: 63: 44: 43: 39:Stereochemistry 24: 19: 17: 12: 11: 5: 1105: 1103: 1095: 1094: 1089: 1084: 1079: 1069: 1068: 1061: 1060: 1055: 1050: 1044: 1041: 1039: 1038: 1033: 1028: 1023: 1018: 1013: 1008: 1003: 998: 992: 989: 987: 986: 981: 976: 971: 966: 959: 957:Steric effects 954: 949: 944: 939: 934: 929: 924: 919: 914: 909: 904: 898: 895: 893: 892: 887: 880: 875: 873:Ray–Dutt twist 870: 865: 860: 854: 851: 849: 848: 843: 841:Pseudorotation 838: 833: 828: 823: 818: 813: 808: 803: 798: 793: 788: 783: 778: 772: 769: 767: 766: 761: 756: 750: 747: 745: 744: 737: 732: 726: 723: 721: 720: 715: 710: 705: 699: 696: 694: 693: 688: 683: 677: 674: 672: 671: 666: 661: 655: 652: 650: 649: 644: 638: 635: 633: 632: 627: 622: 617: 611: 608: 606: 605: 599: 596: 594: 593: 588: 583: 578: 572: 569: 567: 566: 564:Eudysmic ratio 561: 556: 551: 546: 541: 536: 531: 526: 521: 515: 512: 510: 509: 504: 499: 494: 492:Dihedral angle 489: 484: 479: 474: 468: 465: 463: 462: 457: 452: 447: 442: 437: 432: 427: 422: 417: 412: 407: 402: 397: 392: 387: 382: 377: 372: 367: 362: 357: 352: 347: 342: 337: 331: 328: 326: 325: 320: 315: 310: 305: 299: 296: 294: 293: 288: 283: 278: 273: 266: 261: 256: 254:Allylic strain 251: 244: 239: 233: 230: 228: 227: 221: 219: 218: 209: 206: 201: 200: 190: 189: 186: 183: 181: 180: 172:Stereochemists 170: 169: 166: 163: 161: 160: 150: 149: 146: 143: 141: 140: 130: 129: 126: 123: 121: 120: 106: 105: 102: 99: 97: 96: 86: 85: 82: 79: 77: 76: 62: 61: 58: 55: 54: 49: 46: 30: 29: 13: 10: 9: 6: 4: 3: 2: 1104: 1093: 1090: 1088: 1085: 1083: 1080: 1078: 1075: 1074: 1072: 1059: 1056: 1054: 1051: 1049: 1046: 1045: 1042: 1037: 1034: 1032: 1029: 1027: 1024: 1022: 1019: 1017: 1014: 1012: 1009: 1007: 1004: 1002: 999: 997: 994: 993: 990: 985: 982: 980: 977: 975: 972: 970: 967: 964: 963:Steric number 960: 958: 955: 953: 950: 948: 945: 943: 940: 938: 935: 933: 930: 928: 925: 923: 920: 918: 915: 913: 910: 908: 907:Soai reaction 905: 903: 900: 899: 896: 891: 888: 885: 881: 879: 876: 874: 871: 869: 866: 864: 861: 859: 856: 855: 852: 847: 844: 842: 839: 837: 834: 832: 829: 827: 824: 822: 819: 817: 814: 812: 811:Prelog strain 809: 807: 804: 802: 799: 797: 794: 792: 789: 787: 784: 782: 779: 777: 774: 773: 770: 765: 762: 760: 757: 755: 752: 751: 748: 742: 738: 736: 733: 731: 728: 727: 724: 719: 716: 714: 711: 709: 706: 704: 703:Meso compound 701: 700: 697: 692: 689: 687: 684: 682: 679: 678: 675: 670: 667: 665: 662: 660: 657: 656: 653: 648: 645: 643: 640: 639: 636: 631: 628: 626: 625:Homochirality 623: 621: 618: 616: 613: 612: 609: 604: 603:Gauche effect 601: 600: 597: 592: 591:Fuzzy complex 589: 587: 584: 582: 579: 577: 574: 573: 570: 565: 562: 560: 557: 555: 552: 550: 547: 545: 542: 540: 537: 535: 532: 530: 527: 525: 522: 520: 517: 516: 513: 508: 505: 503: 500: 498: 495: 493: 490: 488: 485: 483: 480: 478: 475: 473: 470: 469: 466: 461: 458: 456: 453: 451: 448: 446: 443: 441: 438: 436: 433: 431: 428: 426: 423: 421: 418: 416: 413: 411: 408: 406: 405:Chiral switch 403: 401: 398: 396: 393: 391: 388: 386: 383: 381: 378: 376: 373: 371: 368: 366: 363: 361: 358: 356: 353: 351: 348: 346: 343: 341: 338: 336: 333: 332: 329: 324: 321: 319: 316: 314: 311: 309: 306: 304: 301: 300: 297: 292: 289: 287: 284: 282: 279: 277: 274: 271: 267: 265: 262: 260: 257: 255: 252: 249: 245: 243: 240: 238: 235: 234: 231: 226: 223: 222: 220: 216: 214: 207: 193: 188: 187: 184: 173: 168: 167: 164: 153: 148: 147: 144: 133: 128: 127: 124: 113: 109: 104: 103: 100: 89: 84: 83: 80: 69: 65: 60: 59: 56: 52: 48:Subcategories 47: 41: 40: 35: 27: 16: 1058:VSEPR theory 932:Stereocenter 868:Racemization 858:Racemic acid 816:Prochirality 718:Mutarotation 519:E–Z notation 477:Diastereomer 380:Chiral drugs 303:Bailar twist 242:Akamptisomer 210: 50: 37: 286:Atropisomer 116:(2 C, 28 P) 72:(3 C, 35 P) 1071:Categories 1011:Topoisomer 681:LCP theory 529:Enantiomer 996:Tacticity 890:Ring flip 410:Chirality 112:Isomerism 68:Chirality 1006:Topicity 34:category 92:(128 P) 559:Epimer 259:Anomer 196:(61 P) 176:(29 P) 156:(14 P) 136:(68 P) 1092:Space 620:Hexol 36:is 1073:: 215:. 194:‎ 174:‎ 154:‎ 134:‎ 114:‎ 90:‎ 70:‎ 1043:V 991:T 897:S 853:R 771:P 749:O 725:N 698:M 676:L 654:K 637:I 610:H 598:G 571:F 514:E 467:D 330:C 298:B 232:A 185:Σ 165:S 145:R 125:M 101:I 81:E 57:C 42:.

Index

Chemistry portal
category
Stereochemistry

Chirality
Enantiopure drugs

Isomerism
Molecular geometry
Racemic mixtures
Stereochemists
Stereochemistry stubs
This list may not reflect recent changes
Stereochemistry
Absolute configuration
Akamptisomer
Alkane stereochemistry
Allylic strain
Anomer
Antarafacial and suprafacial
Antipode (chemistry)
Asymmetric carbon
Asymmetric induction
Atropisomer
Axial chirality
Bailar twist
Baldwin's rules
Bent molecular geometry
Bicapped trigonal prismatic molecular geometry
Bredt's rule

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