81028-13-9Relevant articles and documents
A convergent and stereoselective total synthesis of phomolides G and H
Subba Reddy,Sivaramakrishna Reddy,Phaneendra Reddy,Yadav
, p. 501 - 504 (2014/03/21)
A stereoselective total synthesis of phomolides G and H, a polyketide natural products is described. The synthesis involves organocatalytic enantioselective asymmetric epoxidation, C1-Wittig olefination, and ring-closing metathesis as key steps. The use of organocatalytic MacMillan asymmetric epoxidation for the construction of two chiral centers of phomolides G and H makes this approach more attractive. Georg Thieme Verlag Stuttgart New York.
A New Method for the Dehydration of β-Hydroxy Sulfones: Synthesis of (E,S)-γ-Hydroxy-α,β-unsaturated Sulfones and (S)-ε-Hydroxy-(E,E)-α,γ-dienyl Sulfones
Kang, Suk-Ku,Park, Young-Won,Kim, Sung-Gyu,Jeon, Jae-Hoon
, p. 405 - 406 (2007/10/02)
Optically active (E,S)-γ-hydroxy-α,β-unsaturated sulfones and (S)-ε-hydroxy-(E,E)-α,γ-dienyl sulfones have been prepared in a one-pot dehydration procedure from β,γ-dihydroxy sulfones and δ,ε-dihydroxy allyl sulfones, respectively, via an elimination reac
A Convenient Synthesis of Polyoxamic Acid, 5-O-Carbamoylpolyoxamic Acid, and Their Unnantural D Isomers
Saksena, Anil K.,Lovey, Raymond G.,Girijavallabhan, Viyyoor M.,Ganguly, Ashit K.,McPhail, Andrew T.
, p. 5024 - 5028 (2007/10/02)
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