Application of In Situ FTIR for the Preparation of 17-α-Estradiol via Mitsunobu Reaction
Author:
Affiliation:
1. Libbs Farmacêutica Ltda., Rua Alberto Correia Francfort, 88, Embu das Artes, São Paulo 06807461, Brazil
2. Mettler Toledo Ind. e Com. Ltda, Av. Tamboré, 418, Barueri, São Paulo 06460000, Brazil
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.5b00394
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1. 17α-estradiol: a less-feminizing estrogen
2. Development of 17α-Estradiol as a Neuroprotective Therapeutic Agent: Rationale and Results from a Phase I Clinical Study
3. Review of the effects of 17α-estradiol in humans: a less feminizing estrogen with neuroprotective potential
4. An easy stereoselective synthesis of 5(10)-estrene-3β,17α-diol, a biological marker of pregnancy in the mare
5. The Facile Synthesis of 19-Nortestosterone and 19-Norandrostenedione from Estrone
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