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- Q79733511 description "artículu científicu espublizáu en febreru de 2007" @default.
- Q79733511 description "im Februar 2007 veröffentlichter wissenschaftlicher Artikel" @default.
- Q79733511 description "scientific article published on 07 February 2007" @default.
- Q79733511 description "wetenschappelijk artikel" @default.
- Q79733511 description "наукова стаття, опублікована в лютому 2007" @default.
- Q79733511 name "Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaffolds employing inter- and intramolecular mitsunobu reactions" @default.
- Q79733511 name "Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaffolds employing inter- and intramolecular mitsunobu reactions" @default.
- Q79733511 type Item @default.
- Q79733511 label "Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaffolds employing inter- and intramolecular mitsunobu reactions" @default.
- Q79733511 label "Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaffolds employing inter- and intramolecular mitsunobu reactions" @default.
- Q79733511 prefLabel "Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaffolds employing inter- and intramolecular mitsunobu reactions" @default.
- Q79733511 prefLabel "Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaffolds employing inter- and intramolecular mitsunobu reactions" @default.
- Q79733511 P1433 Q79733511-D5C3E8BD-9D5F-4C63-8C20-73782422CBA6 @default.
- Q79733511 P1476 Q79733511-C7E23FEE-D18A-4AF1-A61A-0BF1351A2C7B @default.
- Q79733511 P2093 Q79733511-37C850EB-E503-4133-9166-EDF345B3E539 @default.
- Q79733511 P2093 Q79733511-65B16289-27BC-440D-8EEA-CE6ABBE40CE9 @default.
- Q79733511 P304 Q79733511-3B5AF53E-E240-4D29-B722-419E025D711A @default.
- Q79733511 P31 Q79733511-DBCADA28-9E50-4186-8FDE-743F73B58A5F @default.
- Q79733511 P356 Q79733511-6D9193C0-2C50-453F-B7CC-EF8E58044FB2 @default.
- Q79733511 P433 Q79733511-224E172B-B41B-4047-810A-E6B007A2C051 @default.
- Q79733511 P478 Q79733511-8F81E2C2-47E1-4570-90A5-B1656521DBBD @default.
- Q79733511 P577 Q79733511-AAB4C12C-F414-4972-B999-1EE2A117945E @default.
- Q79733511 P698 Q79733511-2FC0B106-817E-4808-B820-317ECC3E31AD @default.
- Q79733511 P921 Q79733511-89D067A8-F7D4-4A8B-A11C-53A207F9032D @default.
- Q79733511 P356 CC0601480 @default.
- Q79733511 P698 17284080 @default.
- Q79733511 P1433 Q2819062 @default.
- Q79733511 P1476 "Diversity-oriented synthetic approach to naturally abundant S-amino acid based benzannulated enantiomerically pure medium ring heterocyclic scaffolds employing inter- and intramolecular mitsunobu reactions" @default.
- Q79733511 P2093 "Gautam Panda" @default.
- Q79733511 P2093 "Jitendra Kumar Mishra" @default.
- Q79733511 P304 "321-338" @default.
- Q79733511 P31 Q13442814 @default.
- Q79733511 P356 "10.1021/CC0601480" @default.
- Q79733511 P433 "2" @default.
- Q79733511 P478 "9" @default.
- Q79733511 P577 "2007-02-07T00:00:00Z" @default.
- Q79733511 P698 "17284080" @default.
- Q79733511 P921 Q494483 @default.