SFX by Ex Libris Inc.

Title:	Colorado River flow dwindles as warming-driven loss of reflective snow energizes evaporation
Source:	Science [0036-8075] Milly, P. C. D. yr:2020

Basic

Sorry, no full text available...

Please use the document delivery service (see below)

Holding information

Holdings in library search engine ALBERT

Document delivery

Request document via Library/Bibliothek

Users interested in this article also expressed an interest in the following:
description	1.	Mandal, Amit K. "Stereocontrolled Total Synthesis of (-)-Ebelactone A." Organic letters 4.12 (2002): 2043-2045.
description	2.	Koller, W. "Ebelactones inhibit cutinases produced by fungal plant pathogens." The Journal of Antibiotics 43.6 (1990): 734-5.
description	3.	Mehta, G. "Toward a total synthesis of the novel polyketide natural product spiculoic acid A." Organic letters 7.25 (2005): 5569-5572.
description	4.	Archibald, Sarah C. "Stereocontrol in organic synthesis using silicon-containing compounds. Studies directed towards the synthesis of ebelactone A." Organic & biomolecular chemistry 2.7 (2004): 1051-1064.
description	5.	Nakamura, S. "Regio- and chemoselective silylmetalation of functionalized terminal alkenes." Journal of the American Chemical Society 129.1 (2007): 28-29.
description	6.	Paterson, I. "Total Synthesis of (-)-Ebelactone A and B." Journal of organic chemistry 60.11 (1995): 3288-3300.
description	7.	Uotani, K. "Biosynthetic studies of ebelactone A and B by carbon-13 NMR spectrometry." The Journal of Antibiotics 35.12 (1982): 1670-4.
description	8.	Ostrowska, H. "Ebelactone B, an inhibitor of extracellular cathepsin A-type enzyme, suppresses platelet aggregation ex vivo in renovascular hypertensive rats." Journal of cardiovascular pharmacology 45.4 (2005): 348-53.
description	9.	LOWE, C. "NATURALLY-OCCURRING BETA-LACTONES - OCCURRENCE, SYNTHESES AND PROPERTIES - A REVIEW." Organic preparations and procedures international 27.3 (1995): 305-346.
description	10.	Wen, Y. "Identification and analysis of the gene cluster involved in biosynthesis of paenibactin, a catecholate siderophore produced by Paenibacillus elgii B69." Environmental microbiology 13.10 (2011): 2726-2737.
description	11.	Livingstone, M. "A Chemical Genetic Screen for mTOR Pathway Inhibitors Based on 4E-BP-Dependent Nuclear Accumulation of eIF4E." Chemistry & biology 16.12 (2009): 1240-1249.
description	12.	Hulme, Alison N. "Synthesis of Î²-keto phosphonates from thioester intermediates. A stereocontrolled route to the C29-C35 fragment of the halichondramides." Synlett 8 (1998): 828-.
description	13.	Uchiyama, M. "Structure and reaction pathway of TMP-zincate: Amido base or alkyl base?" Journal of the American Chemical Society 128.27 (2006): 8748-8750.
description	14.	Navarro, O. "Suzuki-Miyaura, alpha-ketone arylation and dehalogenation reactions catalyzed by a versatile N-heterocyclic carbene-palladacycle complex." Journal of organic chemistry 71.2 (2006): 685-692.
description	15.	Boeckman, Robert K. "Stereocontrol in the intramolecular Diels-Alder reaction. 7. Use of the trimethylsilyl group as a removable stereocontrol element to provide greatly enhanced levels of diastereoselection." Journal of organic chemistry 50.18 (1985): 3421-3423.
description	16.	Chandrasekhar, S. "Total synthesis of 6-epi-prelactone-V via a syn-selective oxygen tethered intramolecular Michael reaction." Tetrahedron Letters 47.7 (2006): 1213-1215.
description	17.	Angeles Cubillo de Dios, M. "Silyl-cupration of a propargylsilane as a test for the reversibility of a metallo-metallation." Journal of organometallic chemistry 624.1-2 (2001): 69-72.
description	18.	Tsuji, J. "Palladium-catalyzed preparation of Î±-allyl esters and Î±,Î²-unsaturated esters from saturated esters via their ketene silyl acetals." Tetrahedron Letters 25.42 (1984): 4783-4786.
description	19.	Jones, Graeme R. "The Oxidation of the Carbon-Silicon Bond." Tetrahedron 52.22 (1996): 7599-7662.
description	20.	Zapf, Christoph W. "A Diels-Alder macrocyclization enables an efficient asymmetric synthesis of the antibacterial natural product abyssomicin C." Angewandte Chemie 44.40 (2005): 6533-6537.