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By W. Klyne, John B. Buckingham

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Extra resources for Atlas of Stereochemistry: Absolute Configurations of Organic Molecules

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IR)-( -I 2-am•no-1phenyle thanol C(l)~[6] Ph CHPhz C(Zit [7] d1phenylth11ran [2] I I CH 2 NH 2 111 5. (ZR, 3RI-(+)2,3- 4. ) ' I I c"'t> H-C-Ph H-C-Ph H-C-Ph CH 2 NH phenylprOp10111C OCid Kl8 I I I I I [7] I. (51-I- I 3- hydroxy-3- ~Hz ~Hz 'I ' N-~-H I )>" Ph I Ph 18. (51 -I+) a- benzoylbenzylamine ldesylam1ne) 19. 125,351 -I- I 2, 3d1phenylaz~r1dme G. Berti, F. Bottari, P. L. Ferrariniand B. Macchia,J. Org. , 1965,30,4091. P. L. Fereday, and S. F. Mason, Chem. , 1971, 1314. G. G. Lyle and W. Lacroix, J.

11. 12 . 13. [ 4 ][5] H I _ _,COOH 13. (25,45)-(- ) Ntosyl - 2 -t hio-5ozobocyclo - [2 . 2. I) heptane 14. (25,55)-( )2,5diozoblcyclo [2 . 2. 0 heptone 01- HCL ( + ) Class 2a Miscellaneous one- and two-centre compounds O O s ,-COOH S S QR [6] ~OOH __ cooH HOCou HOCOD __ cooH CD QR [4] [3 ] 2-carboxyl•c ac1d Am1de (+) __ cooH se '' C- H, C- H ! - ' CH2 : y- H- 4 . 125,55) - (+) selenophone 2, 5 diCO rboxyi iC OCid 3 . 125,55)-( + ) t h1aphane 2,5 d•corboxyl•c oc•d 2 . (51 - ( +I th1aphane - (5)-1+)1, 2 dlthlalane - 3corboxy llc acid 5 CH3 COOH 5.

5. 6. 7. 8. ' H I CHMe 2 II. (5) - (-)2-hydroxy-3 meth ylbut ync ac1d 10. 5;35) - ( +)2' 3 - d · - I HO - - C- H C- ' ~OOH ~ ~HzOH ' I I CH3 COOH CHMe 2 3,3- domethy lbutyro c oc1dS (X oCL , Br) N0X t[6] Ci 2 )t [ 7J '' I I CMe 3 9. (5 ) -1 + )2 - halogeno - I . I I I 8 . (R)-( - )2- omlno - 3, 3 dlmethylbutone (ponocolylomone ) CMe3 X- [6 ] I CMe 3 H 2 N-~-H CD x - ~-H : . HO - - C-H I' COOH COOH I ' . =·+·· C-OH ~OOH HO -'- C-'-H nydroxybulyroc ac1d COOH I 5 . 6 6. (9R, IORl - I + ) 9,1 0 - d1hydro 9 , I 0 - d 1hyd roxyphenant hrene H 2 N-~-H H- 1 \COOH [4] OH I I CH3 HO _;_ C_ :_ H OH HO ~ H- \ I H -C- ORO <;OOH • •..

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