142 results on '"ERMOLENKO, M. S."'
Search Results
2. Synthesis of macrolide antibiotics. 20. Synthesis of erythronolide A
3. Synthesis of macrolide antibiotics. 14. Synthesis of 1-methylene-3,5-O-isopropylidene-9,11-O-p-(methoxybenzylidene)-9(S)-dihydro derivative of seco acid of 9(S)-dihydroerythronolide B
4. Synthesis of macrocyclic antibiotics. 9. Synthesis of the C9−C13 fragments of 12-epineomethinolide and methinolide
5. Synthesis of macrolide antibiotics. 17. Synthesis of the C1-C10-fragment of erythronolides (A) and (B)
6. Selenoesters in organic synthesis. 1. Conversion of mixed carboxylic acid esters to selenoesters
7. Synthesis of macrolide antibiotics. Communication 8. Synthesis of acyclic forms of C9-C13 fragment of erythronolide B
8. Synthesis of macrolide antibiotics. Communication 6. Synthesis of C13-EPI-C9-C13 fragment of erythronolide a
9. Synthesis of macrolide antibiotics. 13. synthesis of certain derivatives of the seco-acid of erythronolide B
10. Synthesis of C-methyldesoxy sugars: Desoxygenation of tertiary alcohol xanthogenates and hydrozirconation of exomethylene derivatives of carbohydrates
11. Synthesis of macrolide antibiotics. 18. Stereospecific building up of the carbon chain of erythronolide B
12. Synthesis of macrolide antibiotics Communication 1. Synthesis of the C1-C6 fragment of 14-membered macrolide antibiotics
13. Synthesis of macrolide antibiotics. 15. Stereodirected synthesis of erythronolide B according to the coupling scheme of the (C9-C13) + (C7-C8) + (C1-C6) fragments
14. Synthesis of macrolide antibiotics Communication 2. Synthesis of the C9-C13 fragment of erythronolides A and C and megalonolide
15. Synthesis of macrolide antibiotics Communication 3. Synthesis of the C9-C13 fragments of oleandonolide and erythronolide B
16. Synthesis of macrolide antibiotics: 11. Retrosynthetic analysis of erythronolide B and synthesis of the cyclic form of the C1-C6fragment of erythronolides A and B
17. Synthesis of macrolide antibiotics. 16. Synthesis of erythronolides A and B by a coupling scheme of (C5-C9) + (C3-C4) + (C1-C2) + (C10) + (C11-C13) fragments and synthesis of the C5-C9 fragment
18. Selenoesters in organic synthesis. 2. New synthesis of saturated and α,β-unsaturated ketones and the synthesis of the Peach moth pheromone (Carposia niponensis)
19. Synthesis of macrocyclic antibiotics. 10. Synthesis of the C9−C13 fragment of neomethinolide
20. Friedel-Crafts alkylation of indoles
21. Synthesis of macrolide antibiotics.: 12. Synthesis of C1-C8 fragments of erythronolides A and B
22. Synthesis of macrolide antibiotics Communication 7. New synthesis of C9-C13 fragment of erythronolide A
23. Reaction of 3-indolylphenyliodonium betaine with electrophilic agents
24. New method for the synthesis of 2,4-didesoxy-2,4-di-C-methyl-d-glucopyranose derivatives
25. Nucleophilic substitution in iodonium derivatives of indole
26. Peculiarities of nucleophilic substitution in indolyliodonium salts
27. ChemInform Abstract: Stereocontrolled Synthesis of Erythronolides A and B in a (C5-C9) + ( C3-C4) + (C1-C2) + (C11-C13) Sequence from 1,6-Anhydro-β-D- glucopyranose (Levoglucosan). Part 2.
28. ChemInform Abstract: Stereocontrolled Synthesis of Erythronolides A and B in a (C5-C9) + ( C3-C4) + (C1-C2) + (C11-C13) Sequence from 1,6-Anhydro-β-D- glycopyranose (Levoglucosan). Part 1. Synthesis of C1-C10 and C11-C13 Segments.
29. ChemInform Abstract: Stereoselective Synthesis of the Tetrasubstituted Cyclohexane Core ( XII) of a Monocyclic Mevinic Acid Analogue.
30. ChemInform Abstract: Total Synthesis of a Monocyclic Analogue (VIII) of Compactin.
31. ChemInform Abstract: A Convergent Carbohydrate Approach to the Synthesis of Taxol. Part 1. Ring A Subunit.
32. ChemInform Abstract: Intramolecular Horner-Wadsworth-Emmons Olefination Route to Annulated Carbohydrates.
33. ChemInform Abstract: Determination of the Absolute Stereochemistry of the Antifungal Antibiotic YM-47522 by the Total Synthesis of Its Enantiomer.
34. ChemInform Abstract: Synthesis of a C(9)—C(13) Fragment of Acutiphycin from Levoglucosan.
35. ChemInform Abstract: A Convergent Carbohydrate Approach to the Synthesis of Taxol. Part 2. Ring C Subunit.
36. ChemInform Abstract: Synthesis of Macrolide Antibiotics. Part 2. Synthesis of Erythronolide A (I).
37. ChemInform Abstract: Synthesis of Macrolide Antibiotics. Part 19. Synthesis of the C7‐C13‐Fragment of Erythronolide A.
38. Synthesis of the C12−C19 Fragment of (+)-Peloruside A through a Diastereomer-Discriminating RCM Reaction
39. Synthesis of macrolide antibiotics. 16. Synthesis of erythronolides A and B by a coupling scheme of (C5-C9) + (C3-C4) + (C1-C2) + (C10) + (C11-C13) fra
40. Synthesis of macrolide antibiotics. 17. Synthesis of the C1-C10-fragment of erythronolides (A) and (B)
41. Synthesis of macrocyclic antibiotics. 9. Synthesis of the C9−C13 fragments of 12-epineomethinolide and methinolide
42. Synthesis of macrocyclic antibiotics. 10. Synthesis of the C9−C13 fragment of neomethinolide
43. Synthesis of macrolide antibiotics. Communication 8. Synthesis of acyclic forms of C9-C13 fragment of erythronolide B
44. Synthesis of macrolide antibiotics Communication 7. New synthesis of C9-C13 fragment of erythronolide A
45. Synthesis of macrolide antibiotics Communication 2. Synthesis of the C9-C13 fragment of erythronolides A and C and megalonolide
46. Synthesis of macrolide antibiotics Communication 1. Synthesis of the C1-C6 fragment of 14-membered macrolide antibiotics
47. Synthesis of macrolide antibiotics Communication 3. Synthesis of the C9-C13 fragments of oleandonolide and erythronolide B
48. ChemInform Abstract: NUCLEOPHILIC SUBSTITUTION IN IODONIUM DERIVATIVES OF INDOLE
49. ChemInform Abstract: Synthesis of Macrolide Antibiotics. Part 10. Synthesis of the C9-C13Fragment of Neomethinolide.
50. ChemInform Abstract: Stereocontrolled Synthesis of Erythronolides A and B from 1,6‐Anhydro‐β‐D‐glucopyranose (Levoglucosan). Skeleton Assembly in (C9‐C13) + (C7‐C8) + (C1‐C6) Sequence.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.