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1.	Enierga, G, et al. (author) An enantioselective synthesis of (+)-pseudohygroline. 1998 In: TETRAHEDRON LETTERS. - : PERGAMON-ELSEVIER SCIENCE LTD. ; 39:18 Other publication (other academic/artistic)abstract The enantioselective synthesis of (+)-pseudohygroline (3), employing a highly diastereoselective ring closure as a key step, has been achieved in seven steps from readily available protected lactaldehyde (6). (C) 1998 Elsevier Science Ltd. All rights res
2.	Enierga, G, et al. (author) Intramolecular amidomercurations under allylic control: a stereoselective synthesis of (+)-pseudohygroline and (+)-3-hydroxypyrrolizidine 2001 In: TETRAHEDRON-ASYMMETRY. - : PERGAMON-ELSEVIER SCIENCE LTD. - 0957-4166. ; 12:4, s. 597-604 Journal article (peer-reviewed)abstract The diastereoselectivity of intramolecular amidomercurations can be reversed by altering the remote allylic substituent of omega -alkenylcarbamates. This methodology has been applied to the synthesis of (+)-pseudohygroline and (+)-3-hydroxypyrrolizidine.

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Author/Editor: Rose, M. (2); Wong, K (2); Sjoberg, S (2); Perlmutter, P (2); Enierga, G (2); Hockless, DCR (1); show more...; Espiritu, M (1); Pham, N (1); Thienthong, N (1); show less...

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