
(S)-2,6-Bis-tert-butoxycarbonylaminohexanoic acid | CAS:2483-46-7
(S)-2,6-Bis-tert-butoxycarbonylaminohexanoic acid
- Name:(S)-2,6-Bis-tert-butoxycarbonylaminohexanoic acid
- CAS:2483-46-7
- Synonyms:Boc-Lys(Boc)-OH
- Molecular Formula:C16H30N2O6
- Molecular Weight:346.42
- EINESC:
Description
Properties
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Safety
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SDS
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Matrix | View & Download |
Synthetic Route
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Articles
Peer-Reviewed Papers
Asymmetric total synthesis of (+)-aphanamol I based on the transition metal catalyzed [5+ 2] cycloaddition of allenes and vinylcyclopropanes.Wender P A and Zhang L Organic Letters, 2(15), 2323-2326 (2000)
Synthesis of 1?Iodopropyne.Bartko S G, et al. Organic Syntheses, 93, 245-262 (2003)
Gold (I)?Catalyzed Intermolecular [2+ 2] Cycloadditions between Allenamides and Alkenes.Faustino H, et al. Advanced Synthesis & Catalysis, 354(9), 1658-1664 (2012)
Regioconvergent and Enantioselective Rhodium?Catalyzed Hydroamination of Internal and Terminal Alkynes: A Highly Flexible Access to Chiral Pyrazoles.Haydl A M, et al. Chemistry?A European Journal , 22(19), 6547-6551 (2016)
Synthetic scope, computational chemistry and mechanism of a base induced 5-endo cyclization of benzyl alkynyl sulfides.Motto J M, et al. Tetrahedron, 67(5), 1002-1010 (2011)
Facile multi-decagram synthesis of methyl but-2-ynoate.Darses B, et al. Organic Chemistry Frontiers : An International Journal of Organic Chemistry / Royal Society of Chemistry, 1(1), 117-119 (2014)
Total Synthesis of Skyllamycins A?C. Total Synthesis of Natural Products, 119-150 (2018)
Remarks
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Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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