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Results: 1-3 |
Results: 3
The thionophosphate-thiolophosphate photoisomerization proceeds predominantly through a non-chain radical pathway. Synthetically viable benzylation of tetrahydrofuran, propan-2-ol and olefins
Authors: Yadav, VK Balamurugan, R Parvez, M Yamdagni, R
Citation: Vk. Yadav et al., The thionophosphate-thiolophosphate photoisomerization proceeds predominantly through a non-chain radical pathway. Synthetically viable benzylation of tetrahydrofuran, propan-2-ol and olefins, J CHEM S P1, (3), 2001, pp. 323-332
The design and synthesis of a potent Angiotensin II cyclic analogue confirms the ring cluster receptor conformation of the hormone Angiotensin II
Authors: Matsoukas, JM Polevaya, L Ancans, J Mavromoustakos, T Kolocouris, A Roumelioti, P Vlahakos, DV Yamdagni, R Wu, Q Moore, GJ
Citation: Jm. Matsoukas et al., The design and synthesis of a potent Angiotensin II cyclic analogue confirms the ring cluster receptor conformation of the hormone Angiotensin II, BIO MED CH, 8(1), 2000, pp. 1-10
7-hydroxymethyl-6-methyl-1-oxa-4-thiaspiro[4.5]dec-6-ene. Exceptionally high anti to sulfur diastereoselectivity under conditions of Johnson ortho ester Claisen rearrangement favors Cieplak mode of diastereoselection
Authors: Yadav, VK Jeyaraj, DA Parvez, M Yamdagni, R
Citation: Vk. Yadav et al., 7-hydroxymethyl-6-methyl-1-oxa-4-thiaspiro[4.5]dec-6-ene. Exceptionally high anti to sulfur diastereoselectivity under conditions of Johnson ortho ester Claisen rearrangement favors Cieplak mode of diastereoselection, J ORG CHEM, 64(8), 1999, pp. 2928-2932
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